Item | Value |
---|---|
geneid | 8437 |
ensemblid | ENSG00000111344.12 |
hgncid | 9873 |
symbol | RASAL1 |
name | RAS protein activator like 1 |
refseq_nuc | NM_001301202.2 |
refseq_prot | NP_001288131.1 |
ensembl_nuc | ENST00000548055.2 |
ensembl_prot | ENSP00000448510.1 |
mane_status | MANE Select |
chr | chr12 |
start | 113099278 |
end | 113135761 |
strand | - |
ver | v1.2 |
region | chr12:113099278-113135761 |
region5000 | chr12:113094278-113140761 |
regionname0 | RASAL1_chr12_113099278_113135761 |
regionname5000 | RASAL1_chr12_113094278_113140761 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 805 | 222 | 53 | 47 | 83 | 10 | 28 | 60 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002 | 1/0 | 805 | 83 | 25 | 6 | 41 | 3 | 7 | 35 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0003 | 0/0 | 805 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0004 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0005 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0006 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0007 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0008 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0009 | 0/0 | 691 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0010 | 0/0 | 805 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0011 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0012 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0013 | 0/0 | 805 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2418 | 208 | 46 | 45 | 80 | 10 | 26 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0002 | 1/0 | 2418 | 53 | 21 | 5 | 19 | 1 | 6 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0003 | 0/0 | 2418 | 22 | 0 | 0 | 22 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0004 | 0/0 | 2418 | 4 | 3 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0005 | 0/0 | 2418 | 3 | 2 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0006 | 0/0 | 2418 | 3 | 0 | 1 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0007 | 0/0 | 2418 | 3 | 0 | 0 | 2 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0008 | 0/0 | 2418 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0009 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0010 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0011 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0012 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0013 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0014 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0015 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0016 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0017 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0018 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0019 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0020 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0021 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0022 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0023 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0024 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0025 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
c0026 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 951 | 235 | 62 | 50 | 85 | 10 | 27 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0002 | 1/0 | 951 | 62 | 9 | 3 | 42 | 1 | 6 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0003 | 0/0 | 951 | 5 | 5 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0004 | 0/0 | 951 | 5 | 1 | 1 | 0 | 2 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0005 | 0/0 | 951 | 3 | 2 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0006 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0007 | 0/0 | 951 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0008 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0009 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
t0010 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 3 | 6 | 0 | 3 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0002 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0003 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0006 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0008 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2418 | 208 | 46 | 45 | 80 | 10 | 26 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0001c0004 | 0/0 | 2418 | 4 | 3 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0001c0005 | 0/0 | 2418 | 3 | 2 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0001c0007 | 0/0 | 2418 | 3 | 0 | 0 | 2 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0001c0011 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0001c0013 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0001c0017 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0001c0022 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0002c0002 | 1/0 | 2418 | 53 | 21 | 5 | 19 | 1 | 6 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0002c0003 | 0/0 | 2418 | 22 | 0 | 0 | 22 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0002c0006 | 0/0 | 2418 | 3 | 0 | 1 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0002c0008 | 0/0 | 2418 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0002c0018 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0002c0019 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0002c0025 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0003c0010 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0004c0009 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0005c0024 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0006c0021 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0007c0026 | 0/0 | 2418 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0008c0016 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0009c0014 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0010c0012 | 0/0 | 2418 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0011c0015 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0012c0020 | 0/0 | 2418 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 | |
a0013c0023 | 0/0 | 2418 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3368 | 202 | 44 | 45 | 78 | 10 | 24 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0001t0002 | 0/0 | 3368 | 2 | 0 | 0 | 1 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0001t0003 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0001t0008 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0001t0009 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0001t0010 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0004t0001 | 0/0 | 3368 | 4 | 3 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0005t0001 | 0/0 | 3368 | 3 | 2 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0007t0001 | 0/0 | 3368 | 3 | 0 | 0 | 2 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0011t0001 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0013t0001 | 0/0 | 3368 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0017t0001 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0001c0022t0001 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0002t0001 | 0/0 | 3368 | 13 | 10 | 2 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0002t0002 | 1/0 | 3368 | 36 | 7 | 3 | 19 | 1 | 5 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0002t0003 | 0/0 | 3368 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0002t0006 | 0/0 | 3368 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0003t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0003t0002 | 0/0 | 3368 | 21 | 0 | 0 | 21 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0006t0004 | 0/0 | 3368 | 3 | 0 | 1 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0008t0005 | 0/0 | 3368 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0018t0004 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0019t0003 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0002c0025t0004 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0003c0010t0007 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0004c0009t0002 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0005c0024t0003 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0006c0021t0001 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0007c0026t0002 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0008c0016t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0009c0014t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0010c0012t0001 | 0/0 | 3368 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0011c0015t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0012c0020t0002 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
a0013c0023t0005 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | copy fasta | chr12 | 113094278 | 113140761 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 12 | 0 | 3 | 6 | 0 | 3 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0006 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0008 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0004t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0005t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0007t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0007t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0011t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0013t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0017t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0001c0022t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0002t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0006t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0006t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0006t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0008t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0008t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0018t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0019t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0002c0025t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0003c0010t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0004c0009t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0005c0024t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0006c0021t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0007c0026t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0008c0016t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0009c0014t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0010c0012t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0011c0015t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0012c0020t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
a0013c0023t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0006 | t0004 | g0198 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00280 | hp1 | a0002 | c0006 | t0004 | g0203 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00280 | hp2 | a0003 | c0010 | t0007 | g0027 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00438 | hp2 | a0002 | c0003 | t0002 | g0075 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01109 | hp1 | a0001 | c0005 | t0001 | g0160 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01346 | hp1 | a0010 | c0012 | t0001 | g0131 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01358 | hp2 | a0002 | c0006 | t0004 | g0089 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01993 | hp2 | a0001 | c0013 | t0001 | g0223 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02055 | hp1 | a0002 | c0002 | t0006 | g0033 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02071 | hp2 | a0002 | c0003 | t0002 | g0069 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02132 | hp2 | a0009 | c0014 | t0001 | g0091 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02155 | hp1 | a0002 | c0003 | t0002 | g0082 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0243 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02572 | hp2 | a0002 | c0008 | t0005 | g0038 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02615 | hp2 | a0002 | c0002 | t0003 | g0035 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02622 | hp1 | a0001 | c0017 | t0001 | g0226 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02622 | hp2 | a0004 | c0009 | t0002 | g0036 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02698 | hp2 | a0001 | c0001 | t0010 | g0247 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0181 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02738 | hp2 | a0001 | c0011 | t0001 | g0102 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0242 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02976 | hp1 | a0006 | c0021 | t0001 | g0216 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0166 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0241 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03139 | hp1 | a0001 | c0022 | t0001 | g0103 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03209 | hp1 | a0002 | c0018 | t0004 | g0040 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03209 | hp2 | a0001 | c0005 | t0001 | g0221 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03486 | hp2 | a0002 | c0019 | t0003 | g0032 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0245 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04115 | hp1 | a0001 | c0007 | t0001 | g0083 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04184 | hp2 | a0002 | c0025 | t0004 | g0113 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG04228 | hp2 | a0013 | c0023 | t0005 | g0120 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18522 | hp1 | a0001 | c0005 | t0001 | g0162 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18945 | hp2 | a0001 | c0007 | t0001 | g0072 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18946 | hp2 | a0002 | c0003 | t0002 | g0078 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18949 | hp1 | a0011 | c0015 | t0001 | g0156 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18950 | hp1 | a0008 | c0016 | t0001 | g0106 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18950 | hp2 | a0001 | c0001 | t0009 | g0210 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18951 | hp1 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18954 | hp1 | a0002 | c0003 | t0002 | g0081 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18956 | hp1 | a0002 | c0003 | t0002 | g0237 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18957 | hp1 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0074 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18969 | hp1 | a0002 | c0003 | t0002 | g0064 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18969 | hp2 | a0012 | c0020 | t0002 | g0054 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18974 | hp2 | a0002 | c0003 | t0002 | g0085 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18977 | hp2 | a0002 | c0003 | t0002 | g0077 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18979 | hp2 | a0002 | c0003 | t0002 | g0068 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18984 | hp1 | a0001 | c0004 | t0001 | g0192 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18984 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18992 | hp2 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19043 | hp1 | a0007 | c0026 | t0002 | g0046 | AFR | LWK | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19043 | hp2 | a0002 | c0002 | t0006 | g0030 | AFR | LWK | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19063 | hp1 | a0002 | c0003 | t0002 | g0084 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19064 | hp1 | a0002 | c0003 | t0002 | g0119 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19065 | hp1 | a0001 | c0007 | t0001 | g0070 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19066 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19070 | hp1 | a0002 | c0003 | t0002 | g0079 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19074 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19075 | hp1 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ASW | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA20129 | hp2 | a0005 | c0024 | t0003 | g0034 | AFR | ASW | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0183 | EUR | TSI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG02559 | hp2 | a0002 | c0002 | t0003 | g0028 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03471 | hp1 | a0002 | c0008 | t0005 | g0039 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0206 | REF | REF | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0182 | REF | REF | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:113103975 | C | T | 1 | a0009 | 1 | HG02132.hp2 | stop_gained | HIGH | c.2075G>A | p.Trp692* | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/21 | 2374/3368 | 2075/2418 | 692/805 | chr12 | 113103975 | ||
chr12:113105737 | A | G | 1 | a0010 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1807T>C | p.Phe603Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2106/3368 | 1807/2418 | 603/805 | chr12 | 113105737 | ||
chr12:113105800 | C | G | 1 | a0011 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1744G>C | p.Gly582Arg | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2043/3368 | 1744/2418 | 582/805 | chr12 | 113105800 | ||
chr12:113105802 | G | C | 1 | a0011 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1742C>G | p.Ala581Gly | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2041/3368 | 1742/2418 | 581/805 | chr12 | 113105802 | ||
chr12:113105803 | C | A | 1 | a0011 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1741G>T | p.Ala581Ser | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2040/3368 | 1741/2418 | 581/805 | chr12 | 113105803 | ||
chr12:113107125 | G | C | 1 | a0012 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1629C>G | p.Asp543Glu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/21 | 1928/3368 | 1629/2418 | 543/805 | chr12 | 113107125 | ||
chr12:113112093 | T | G | 1 | a0008 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.1367A>C | p.Glu456Ala | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/21 | 1666/3368 | 1367/2418 | 456/805 | chr12 | 113112093 | ||
chr12:113115676 | C | T | 7 | a0001a0005a0006others(4): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
missense_variant | MODERATE | c.962G>A | p.Arg321His | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/21 | 1261/3368 | 962/2418 | 321/805 | chr12 | 113115676 | ||
chr12:113116005 | G | A | 2 | a0006a0007 | 2 | HG02976.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.778C>T | p.Arg260Cys | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/21 | 1077/3368 | 778/2418 | 260/805 | chr12 | 113116005 | ||
chr12:113127832 | G | A | 1 | a0013 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.278C>T | p.Ala93Val | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 577/3368 | 278/2418 | 93/805 | chr12 | 113127832 | ||
chr12:113127847 | G | A | 1 | a0005 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.263C>T | p.Ser88Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 562/3368 | 263/2418 | 88/805 | chr12 | 113127847 | ||
chr12:113128128 | G | A | 1 | a0003 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.173C>T | p.Thr58Met | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/21 | 472/3368 | 173/2418 | 58/805 | chr12 | 113128128 | ||
chr12:113135432 | C | G | 2 | a0003a0004 | 2 | HG00280.hp2 HG02622.hp2 |
missense_variant | MODERATE | c.31G>C | p.Val11Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 330/3368 | 31/2418 | 11/805 | chr12 | 113135432 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:113099959 | C | T | 1 | a0002c0018 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.2388G>A | p.Gly796Gly | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 2687/3368 | 2388/2418 | 796/805 | chr12 | 113099959 | ||
chr12:113099968 | C | T | 4 | a0002c0006a0002c0018a0002c0025others(1): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
synonymous_variant | LOW | c.2379G>A | p.Gln793Gln | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 2678/3368 | 2379/2418 | 793/805 | chr12 | 113099968 | ||
chr12:113102008 | G | A | 1 | a0001c0005 | 3 | HG01109.hp1 HG03209.hp2 NA18522.hp1 |
splice_region_variant&synonymous_variant | LOW | c.2106C>T | p.Ala702Ala | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/21 | 2405/3368 | 2106/2418 | 702/805 | chr12 | 113102008 | ||
chr12:113103995 | A | T | 1 | a0011c0015 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.2055T>A | p.Gly685Gly | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/21 | 2354/3368 | 2055/2418 | 685/805 | chr12 | 113103995 | ||
chr12:113104194 | C | T | 1 | a0001c0013 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.1935G>A | p.Thr645Thr | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/21 | 2234/3368 | 1935/2418 | 645/805 | chr12 | 113104194 | ||
chr12:113104293 | A | G | 5 | a0002c0006a0002c0008a0002c0018others(2): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
synonymous_variant | LOW | c.1836T>C | p.Cys612Cys | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/21 | 2135/3368 | 1836/2418 | 612/805 | chr12 | 113104293 | ||
chr12:113105753 | G | A | 1 | a0002c0019 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1791C>T | p.Ser597Ser | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2090/3368 | 1791/2418 | 597/805 | chr12 | 113105753 | ||
chr12:113114889 | G | A | 1 | a0001c0017 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1092C>T | p.His364His | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/21 | 1391/3368 | 1092/2418 | 364/805 | chr12 | 113114889 | ||
chr12:113117141 | G | A | 3 | a0002c0006a0002c0025a0003c0010 | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
synonymous_variant | LOW | c.663C>T | p.Thr221Thr | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/21 | 962/3368 | 663/2418 | 221/805 | chr12 | 113117141 | ||
chr12:113127822 | G | A | 1 | a0001c0022 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.288C>T | p.Ala96Ala | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 587/3368 | 288/2418 | 96/805 | chr12 | 113127822 | ||
chr12:113127858 | G | A | 1 | a0002c0025 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.252C>T | p.Ile84Ile | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 551/3368 | 252/2418 | 84/805 | chr12 | 113127858 | ||
chr12:113127870 | G | A | 2 | a0001c0004a0007c0026 | 5 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(2): Show |
synonymous_variant | LOW | c.240C>T | p.His80His | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 539/3368 | 240/2418 | 80/805 | chr12 | 113127870 | ||
chr12:113128084 | G | A | 2 | a0001c0007a0002c0003 | 25 | HG00438.hp2 HG02071.hp2 HG02155.hp1 others(22): Show |
synonymous_variant | LOW | c.217C>T | p.Leu73Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/21 | 516/3368 | 217/2418 | 73/805 | chr12 | 113128084 | ||
chr12:113128127 | C | T | 1 | a0001c0011 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.174G>A | p.Thr58Thr | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/21 | 473/3368 | 174/2418 | 58/805 | chr12 | 113128127 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:113099321 | G | A | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(25): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*608C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 608 | chr12 | 113099321 | |||||
chr12:113099416 | C | T | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(22): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 513 | chr12 | 113099416 | |||||
chr12:113099418 | C | G | 1 | a0001c0001t0009 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 511 | chr12 | 113099418 | |||||
chr12:113099553 | C | T | 4 | a0002c0006t0004a0002c0018t0004a0002c0025t0004others(1): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*376G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 376 | chr12 | 113099553 | |||||
chr12:113099757 | C | T | 4 | a0002c0006t0004a0002c0018t0004a0002c0025t0004others(1): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*172G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 172 | chr12 | 113099757 | |||||
chr12:113135652 | C | G | 1 | a0003c0010t0007 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-190G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 190 | chr12 | 113135652 | |||||
chr12:113135682 | T | G | 1 | a0001c0001t0010 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-220A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 220 | chr12 | 113135682 | |||||
chr12:113135695 | A | C | 7 | a0001c0001t0003a0001c0001t0008a0002c0002t0003others(4): Show | 9 | HG00280.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-233T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 233 | chr12 | 113135695 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:113100147 | T | C | 2 | a0002c0002t0001g0042a0002c0019t0003g0032 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2279-79A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100147 | ||||||
chr12:113100228 | T | C | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2279-160A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100228 | ||||||
chr12:113100262 | T | C | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2279-194A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100262 | ||||||
chr12:113100309 | T | G | 4 | a0001c0001t0008g0031a0002c0008t0005g0038a0002c0008t0005g0039others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2279-241A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100309 | ||||||
chr12:113100359 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2278+269G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100359 | ||||||
chr12:113100407 | T | C | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2278+221A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100407 | ||||||
chr12:113100407 | T | G | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2278+221A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100407 | ||||||
chr12:113100610 | A | T | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2278+18T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100610 | ||||||
chr12:113100793 | C | CCAT | 3 | a0001c0001t0001g0171a0001c0001t0001g0187a0001c0001t0001g0232 | 3 | NA18992.hp1 NA19009.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2226-116_2226-114d others(5): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113100793 | ||||||
chr12:113101011 | T | C | 2 | a0002c0002t0001g0042a0002c0019t0003g0032 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2226-331A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101011 | ||||||
chr12:113101182 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2226-502C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101182 | ||||||
chr12:113101196 | A | T | 2 | a0002c0002t0001g0042a0002c0019t0003g0032 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2226-516T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101196 | ||||||
chr12:113101267 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2226-587G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101267 | ||||||
chr12:113101433 | A | T | 2 | a0001c0001t0001g0139a0013c0023t0005g0120 | 2 | HG04228.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2225+456T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101433 | ||||||
chr12:113101571 | C | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.2225+318G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101571 | ||||||
chr12:113101656 | GCTCCAGG others(40): Show |
G | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2225+186_2225+232d others(49): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101656 | ||||||
chr12:113101759 | T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0127others(15): Show | 24 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2225+130A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101759 | ||||||
chr12:113102017 | A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
splice_region_variant&intron_variant | LOW | c.2105-8T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102017 | ||||||
chr12:113102024 | C | T | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2105-15G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102024 | ||||||
chr12:113102067 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2105-58G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102067 | ||||||
chr12:113102079 | C | A | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2105-70G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102079 | ||||||
chr12:113102144 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2105-135C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102144 | ||||||
chr12:113102170 | C | G | 6 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(3): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2105-161G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102170 | ||||||
chr12:113102207 | A | G | 1 | a0002c0025t0004g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2105-198T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102207 | ||||||
chr12:113102296 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2105-287C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102296 | ||||||
chr12:113102468 | G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2105-459C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102468 | ||||||
chr12:113102567 | C | A | 10 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2105-558G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102567 | ||||||
chr12:113102580 | C | T | 1 | a0002c0002t0001g0153 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2105-571G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102580 | ||||||
chr12:113102595 | G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2105-586C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102595 | ||||||
chr12:113102681 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2105-672G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102681 | ||||||
chr12:113102711 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2105-702G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102711 | ||||||
chr12:113102725 | A | G | 1 | a0002c0002t0006g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2105-716T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102725 | ||||||
chr12:113102750 | T | G | 1 | a0001c0001t0001g0019 | 2 | HG01099.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2105-741A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102750 | ||||||
chr12:113102828 | A | G | 7 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(4): Show | 8 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2105-819T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102828 | ||||||
chr12:113102829 | C | T | 7 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(4): Show | 8 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2105-820G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102829 | ||||||
chr12:113102912 | A | G | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2105-903T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102912 | ||||||
chr12:113102958 | C | T | 2 | a0002c0008t0005g0038a0002c0008t0005g0039 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2105-949G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102958 | ||||||
chr12:113103174 | TTTATATA others(3): Show |
T | 1 | a0002c0019t0003g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2104+762_2104+771d others(12): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103174 | ||||||
chr12:113103178 | T | C | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2104+768A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103178 | ||||||
chr12:113103179 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2104+767T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103179 | ||||||
chr12:113103187 | T | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+759A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103187 | ||||||
chr12:113103234 | GTTA | G | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+709_2104+711d others(5): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103234 | ||||||
chr12:113103282 | T | C | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2104+664A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103282 | ||||||
chr12:113103343 | G | C | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+603C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103343 | ||||||
chr12:113103419 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2104+527T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103419 | ||||||
chr12:113103426 | G | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+520C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103426 | ||||||
chr12:113103605 | C | CA | 29 | a0001c0001t0001g0090a0001c0001t0001g0170a0001c0001t0001g0175others(26): Show | 35 | HG00642.hp1 HG01123.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.2104+340dupT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103605 | ||||||
chr12:113103659 | A | G | 7 | a0002c0002t0001g0020a0002c0002t0001g0152a0002c0002t0001g0153others(4): Show | 8 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+287T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103659 | ||||||
chr12:113103669 | A | G | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2104+277T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103669 | ||||||
chr12:113103891 | C | A | 1 | a0011c0015t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2104+55G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103891 | ||||||
chr12:113104099 | C | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1969-18G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/20 | chr12 | 113104099 | ||||||
chr12:113104135 | C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1968+26G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/20 | chr12 | 113104135 | ||||||
chr12:113104626 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1831-328G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104626 | ||||||
chr12:113104646 | C | T | 2 | a0002c0002t0001g0042a0002c0019t0003g0032 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1831-348G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104646 | ||||||
chr12:113104657 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1831-359C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104657 | ||||||
chr12:113104712 | G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1831-414C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104712 | ||||||
chr12:113104740 | G | A | 1 | a0002c0002t0006g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1831-442C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104740 | ||||||
chr12:113104743 | C | G | 1 | a0013c0023t0005g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1831-445G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104743 | ||||||
chr12:113104752 | C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1831-454G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104752 | ||||||
chr12:113104754 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1831-456C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104754 | ||||||
chr12:113104803 | C | T | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1831-505G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104803 | ||||||
chr12:113104904 | A | G | 2 | a0002c0008t0005g0038a0002c0008t0005g0039 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1831-606T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104904 | ||||||
chr12:113105056 | A | G | 1 | a0002c0019t0003g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1830+658T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105056 | ||||||
chr12:113105155 | G | A | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1830+559C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105155 | ||||||
chr12:113105202 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1830+512G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105202 | ||||||
chr12:113105308 | C | T | 1 | a0001c0001t0008g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1830+406G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105308 | ||||||
chr12:113105309 | G | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1830+405C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105309 | ||||||
chr12:113105418 | T | C | 3 | a0002c0002t0001g0096a0002c0002t0001g0097a0002c0002t0001g0240 | 3 | HG00642.hp1 HG00733.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1830+296A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105418 | ||||||
chr12:113105426 | A | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1830+288T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105426 | ||||||
chr12:113105472 | G | A | 6 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(3): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1830+242C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105472 | ||||||
chr12:113105508 | G | A | 1 | a0002c0002t0002g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1830+206C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105508 | ||||||
chr12:113105697 | G | A | 1 | a0002c0002t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1830+17C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105697 | ||||||
chr12:113105936 | G | T | 1 | a0005c0024t0003g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1658-50C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113105936 | ||||||
chr12:113106023 | G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1658-137C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106023 | ||||||
chr12:113106077 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1658-191C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106077 | ||||||
chr12:113106127 | G | T | 10 | a0002c0002t0001g0020a0002c0002t0001g0096a0002c0002t0001g0097others(7): Show | 11 | HG00642.hp1 HG00733.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1658-241C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106127 | ||||||
chr12:113106146 | C | G | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1658-260G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106146 | ||||||
chr12:113106147 | C | A | 1 | a0005c0024t0003g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1658-261G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106147 | ||||||
chr12:113106219 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1658-333C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106219 | ||||||
chr12:113106262 | C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1658-376G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106262 | ||||||
chr12:113106371 | C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1658-485G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106371 | ||||||
chr12:113106384 | A | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1658-498T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106384 | ||||||
chr12:113106564 | C | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1657+533G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106564 | ||||||
chr12:113106572 | G | A | 10 | a0002c0002t0001g0020a0002c0002t0001g0096a0002c0002t0001g0097others(7): Show | 11 | HG00642.hp1 HG00733.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1657+525C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106572 | ||||||
chr12:113106650 | C | CT | 12 | a0001c0001t0001g0092a0001c0001t0001g0194a0001c0001t0008g0031others(9): Show | 12 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1657+446dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106650 | ||||||
chr12:113106747 | G | C | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1657+350C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106747 | ||||||
chr12:113106765 | TTC | T | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1657+330_1657+331d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106765 | ||||||
chr12:113106827 | G | A | 1 | a0005c0024t0003g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1657+270C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106827 | ||||||
chr12:113107038 | C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0174 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1657+59G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113107038 | ||||||
chr12:113107069 | C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1657+28G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113107069 | ||||||
chr12:113107266 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1513-25G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107266 | ||||||
chr12:113107267 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1513-26C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107267 | ||||||
chr12:113107360 | T | C | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1513-119A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107360 | ||||||
chr12:113107388 | C | T | 2 | a0002c0003t0002g0080a0002c0003t0002g0081 | 2 | NA18954.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1513-147G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107388 | ||||||
chr12:113107426 | G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1513-185C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107426 | ||||||
chr12:113107442 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1513-201C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107442 | ||||||
chr12:113107588 | A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1513-347T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107588 | ||||||
chr12:113107687 | T | C | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1512+398A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107687 | ||||||
chr12:113107771 | A | C | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+314T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107771 | ||||||
chr12:113107773 | G | GC | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+311_1512+312i others(3): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107773 | ||||||
chr12:113107774 | G | A | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1512+311C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107774 | ||||||
chr12:113107805 | C | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+280G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107805 | ||||||
chr12:113107892 | T | C | 1 | a0002c0002t0002g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1512+193A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107892 | ||||||
chr12:113107953 | G | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+132C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107953 | ||||||
chr12:113107982 | A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1512+103T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107982 | ||||||
chr12:113108355 | G | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-133C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108355 | ||||||
chr12:113108427 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1375-205A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108427 | ||||||
chr12:113108451 | T | G | 1 | a0001c0001t0001g0133 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1375-229A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108451 | ||||||
chr12:113108620 | C | T | 1 | a0002c0002t0006g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1375-398G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108620 | ||||||
chr12:113108672 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1375-450C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108672 | ||||||
chr12:113108740 | A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1375-518T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108740 | ||||||
chr12:113108828 | T | C | 2 | a0001c0001t0008g0031a0002c0002t0001g0042 | 2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1375-606A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108828 | ||||||
chr12:113108837 | C | CT | 6 | a0002c0002t0002g0181a0002c0006t0004g0089a0002c0006t0004g0198others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-616dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108837 | ||||||
chr12:113108837 | CT | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1375-616delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108837 | ||||||
chr12:113108837 | CTT | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0095others(8): Show | 12 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1375-617_1375-616d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108837 | ||||||
chr12:113108875 | T | C | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-653A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108875 | ||||||
chr12:113109035 | TTGTGTG | T | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-819_1375-814d others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109035 | ||||||
chr12:113109037 | G | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1375-815C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109037 | ||||||
chr12:113109039 | G | T | 2 | a0001c0001t0001g0018a0001c0001t0008g0031 | 3 | HG02602.hp2 HG02809.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1375-817C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109039 | ||||||
chr12:113109043 | G | T | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-821C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109043 | ||||||
chr12:113109043 | GT | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(92): Show | 128 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1375-822delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109043 | ||||||
chr12:113109043 | GTT | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(108): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1375-823_1375-822d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109043 | ||||||
chr12:113109045 | T | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0229a0002c0003t0002g0076 | 4 | HG01515.hp2 HG02602.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-823A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109045 | ||||||
chr12:113109046 | T | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0093a0001c0001t0001g0218others(6): Show | 10 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1375-824A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109046 | ||||||
chr12:113109047 | T | G | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1375-825A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109047 | ||||||
chr12:113109048 | T | G | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1375-826A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109048 | ||||||
chr12:113109059 | T | A | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-837A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109059 | ||||||
chr12:113109124 | A | G | 1 | a0002c0008t0005g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1375-902T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109124 | ||||||
chr12:113109128 | G | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-906C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109128 | ||||||
chr12:113109133 | A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1375-911T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109133 | ||||||
chr12:113109211 | C | T | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-989G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109211 | ||||||
chr12:113109215 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1375-993G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109215 | ||||||
chr12:113109618 | G | C | 2 | a0002c0008t0005g0038a0002c0008t0005g0039 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1375-1396C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109618 | ||||||
chr12:113109681 | G | A | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1375-1459C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109681 | ||||||
chr12:113109756 | G | T | 1 | a0008c0016t0001g0106 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1375-1534C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109756 | ||||||
chr12:113109904 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1375-1682T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109904 | ||||||
chr12:113109909 | C | A | 1 | a0013c0023t0005g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1375-1687G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109909 | ||||||
chr12:113109951 | G | A | 1 | a0006c0021t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1375-1729C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109951 | ||||||
chr12:113109960 | G | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-1738C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109960 | ||||||
chr12:113109977 | G | C | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-1755C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109977 | ||||||
chr12:113110005 | C | A | 4 | a0001c0001t0008g0031a0002c0002t0001g0042a0002c0002t0006g0033others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375-1783G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110005 | ||||||
chr12:113110354 | G | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+1732C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110354 | ||||||
chr12:113110438 | T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(34): Show | 58 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1374+1648A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110438 | ||||||
chr12:113110448 | T | C | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+1638A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110448 | ||||||
chr12:113110499 | G | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0093 | 3 | HG02015.hp1 HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1374+1587C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110499 | ||||||
chr12:113110570 | A | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1374+1516T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110570 | ||||||
chr12:113110582 | T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(34): Show | 58 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1374+1504A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110582 | ||||||
chr12:113110614 | T | A | 1 | a0001c0001t0008g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1374+1472A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110614 | ||||||
chr12:113110668 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1374+1418G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110668 | ||||||
chr12:113111071 | A | G | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+1015T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111071 | ||||||
chr12:113111074 | T | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1374+1012A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111074 | ||||||
chr12:113111094 | CTG | C | 14 | a0001c0001t0001g0025a0001c0001t0001g0101a0001c0001t0001g0107others(11): Show | 15 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1374+990_1374+991d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111094 | ||||||
chr12:113111098 | T | C | 13 | a0001c0001t0008g0031a0002c0002t0001g0042a0002c0002t0006g0033others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1374+988A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111098 | ||||||
chr12:113111118 | G | A | 1 | a0005c0024t0003g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1374+968C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111118 | ||||||
chr12:113111217 | G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0124 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1374+869C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111217 | ||||||
chr12:113111322 | G | C | 1 | a0002c0002t0001g0096 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1374+764C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111322 | ||||||
chr12:113111610 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1374+476A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111610 | ||||||
chr12:113111913 | A | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+173T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111913 | ||||||
chr12:113112028 | G | T | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1374+58C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113112028 | ||||||
chr12:113112382 | C | A | 1 | a0002c0002t0002g0183 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1182-104G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112382 | ||||||
chr12:113112530 | C | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-252G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112530 | ||||||
chr12:113112541 | C | G | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-263G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112541 | ||||||
chr12:113112649 | C | G | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1182-371G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112649 | ||||||
chr12:113112766 | C | T | 1 | a0002c0002t0002g0166 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1182-488G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112766 | ||||||
chr12:113112812 | C | T | 1 | a0001c0001t0008g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1182-534G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112812 | ||||||
chr12:113112866 | C | T | 5 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(2): Show | 5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-588G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112866 | ||||||
chr12:113112939 | G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0213 | 2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1182-661C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112939 | ||||||
chr12:113112954 | A | AAAAT | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-680_1182-677d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | ||||||
chr12:113112954 | A | AAAATAAA others(1): Show |
163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1182-684_1182-677d others(10): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | ||||||
chr12:113112954 | A | AAAATAAA others(5): Show |
5 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0001t0001g0128others(2): Show | 5 | HG04228.hp1 NA18946.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-688_1182-677d others(14): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | ||||||
chr12:113112954 | A | AAAATAAA others(9): Show |
1 | a0002c0002t0006g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1182-692_1182-677d others(18): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | ||||||
chr12:113112954 | A | AAAATAAA others(13): Show |
2 | a0002c0002t0001g0042a0002c0019t0003g0032 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1182-696_1182-677d others(22): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | ||||||
chr12:113112954 | A | AAAATAAA others(17): Show |
1 | a0001c0001t0008g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1182-677_1182-676i others(26): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | ||||||
chr12:113113048 | G | A | 1 | a0002c0002t0006g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1182-770C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113048 | ||||||
chr12:113113204 | C | T | 1 | a0010c0012t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1182-926G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113204 | ||||||
chr12:113113316 | G | A | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-1038C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113316 | ||||||
chr12:113113365 | C | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-1087G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113365 | ||||||
chr12:113113428 | A | G | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-1150T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113428 | ||||||
chr12:113113587 | A | G | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181+1213T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113587 | ||||||
chr12:113113654 | T | C | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1181+1146A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113654 | ||||||
chr12:113113720 | C | T | 8 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181+1080G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113720 | ||||||
chr12:113113812 | C | A | 1 | a0001c0001t0008g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1181+988G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113812 | ||||||
chr12:113113883 | T | C | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+917A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113883 | ||||||
chr12:113113920 | A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1181+880T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113920 | ||||||
chr12:113113991 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1181+809T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113991 | ||||||
chr12:113114189 | T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1181+611A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114189 | ||||||
chr12:113114243 | C | T | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1181+557G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114243 | ||||||
chr12:113114298 | C | A | 2 | a0002c0002t0006g0033a0002c0019t0003g0032 | 2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+502G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114298 | ||||||
chr12:113114335 | A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1181+465T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114335 | ||||||
chr12:113114410 | G | A | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1181+390C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114410 | ||||||
chr12:113114420 | G | A | 1 | a0013c0023t0005g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1181+380C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114420 | ||||||
chr12:113114465 | C | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1181+335G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114465 | ||||||
chr12:113114473 | CA | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1181+326delT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114473 | ||||||
chr12:113114473 | CAA | C | 13 | a0001c0001t0001g0185a0001c0001t0001g0207a0002c0002t0002g0026others(10): Show | 14 | HG01168.hp1 HG01168.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1181+325_1181+326d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114473 | ||||||
chr12:113114491 | A | G | 1 | a0001c0007t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1181+309T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114491 | ||||||
chr12:113114494 | A | G | 1 | a0002c0002t0006g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1181+306T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114494 | ||||||
chr12:113114566 | C | T | 2 | a0002c0002t0006g0033a0002c0019t0003g0032 | 2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+234G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114566 | ||||||
chr12:113114590 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1181+210G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114590 | ||||||
chr12:113114652 | G | A | 8 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(5): Show | 9 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181+148C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114652 | ||||||
chr12:113114746 | T | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0059a0011c0015t0001g0156 | 3 | NA18946.hp1 NA18949.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1181+54A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114746 | ||||||
chr12:113115009 | G | T | 9 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(6): Show | 10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1069-97C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115009 | ||||||
chr12:113115076 | G | A | 1 | a0002c0002t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1068+124C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115076 | ||||||
chr12:113115110 | G | A | 9 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(6): Show | 10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1068+90C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115110 | ||||||
chr12:113115180 | G | C | 9 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(6): Show | 10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1068+20C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115180 | ||||||
chr12:113115446 | C | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0148a0001c0001t0001g0169others(1): Show | 4 | HG01192.hp2 HG01255.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004-182G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115446 | ||||||
chr12:113115460 | C | T | 2 | a0002c0008t0005g0038a0002c0008t0005g0039 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1003+175G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115460 | ||||||
chr12:113115543 | C | T | 9 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(6): Show | 10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1003+92G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115543 | ||||||
chr12:113115603 | C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1003+32G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115603 | ||||||
chr12:113115615 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1003+20C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115615 | ||||||
chr12:113115624 | G | A | 2 | a0002c0008t0005g0038a0002c0008t0005g0039 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1003+11C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115624 | ||||||
chr12:113115819 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-31G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115819 | ||||||
chr12:113115847 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.850-59G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115847 | ||||||
chr12:113115862 | G | A | 3 | a0002c0002t0003g0028a0002c0002t0006g0033a0002c0019t0003g0032 | 3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+72C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115862 | ||||||
chr12:113115869 | AG | A | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+64delC | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115869 | ||||||
chr12:113116091 | C | T | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.732-40G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116091 | ||||||
chr12:113116095 | C | T | 19 | a0002c0002t0002g0007a0002c0002t0002g0012a0002c0002t0002g0013others(16): Show | 24 | HG01123.hp1 HG02040.hp2 HG02148.hp1 others(21): Show |
intron_variant | MODIFIER | c.732-44G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116095 | ||||||
chr12:113116107 | C | T | 1 | a0001c0001t0008g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.732-56G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116107 | ||||||
chr12:113116180 | AC | A | 8 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(5): Show | 9 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.732-130delG | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116180 | ||||||
chr12:113116230 | C | T | 1 | a0002c0002t0002g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.732-179G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116230 | ||||||
chr12:113116319 | C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0190a0001c0001t0001g0214 | 3 | HG02630.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.732-268G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116319 | ||||||
chr12:113116593 | G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0178 | 2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.731+480C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116593 | ||||||
chr12:113116624 | A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.731+449T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116624 | ||||||
chr12:113116677 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.731+396C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116677 | ||||||
chr12:113116803 | G | C | 1 | a0002c0003t0002g0067 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.731+270C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116803 | ||||||
chr12:113116810 | G | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.731+263C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116810 | ||||||
chr12:113116884 | G | A | 14 | a0001c0001t0001g0025a0001c0001t0001g0101a0001c0001t0001g0107others(11): Show | 15 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.731+189C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116884 | ||||||
chr12:113116908 | T | C | 9 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(6): Show | 10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.731+165A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116908 | ||||||
chr12:113117028 | C | T | 6 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(3): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.731+45G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113117028 | ||||||
chr12:113117311 | TC | T | 6 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(3): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-151delG | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117311 | ||||||
chr12:113117495 | T | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.643-334A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117495 | ||||||
chr12:113117742 | A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.643-581T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117742 | ||||||
chr12:113117840 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.643-679G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117840 | ||||||
chr12:113117873 | G | GT | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-713dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117873 | ||||||
chr12:113118051 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.643-890G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118051 | ||||||
chr12:113118060 | T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 5 | HG02258.hp2 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-899A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118060 | ||||||
chr12:113118581 | G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.642+547C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118581 | ||||||
chr12:113118608 | G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0127a0001c0001t0001g0138others(8): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.642+520C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118608 | ||||||
chr12:113118894 | G | C | 1 | a0002c0002t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.642+234C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118894 | ||||||
chr12:113119000 | C | G | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+128G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113119000 | ||||||
chr12:113119267 | C | T | 1 | a0002c0006t0004g0203 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.511-8G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 6/20 | chr12 | 113119267 | ||||||
chr12:113119268 | G | A | 10 | a0002c0002t0001g0020a0002c0002t0001g0096a0002c0002t0001g0097others(7): Show | 11 | HG00642.hp1 HG00733.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-9C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 6/20 | chr12 | 113119268 | ||||||
chr12:113119584 | C | T | 1 | a0002c0002t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.429-141G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119584 | ||||||
chr12:113119596 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.429-153G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119596 | ||||||
chr12:113119772 | TG | T | 6 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-330delC | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119772 | ||||||
chr12:113119809 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-366G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119809 | ||||||
chr12:113119870 | A | G | 2 | a0002c0003t0002g0071a0002c0003t0002g0073 | 2 | NA18951.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.429-427T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119870 | ||||||
chr12:113120069 | A | G | 8 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(5): Show | 9 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-626T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120069 | ||||||
chr12:113120172 | G | C | 6 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(3): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.429-729C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120172 | ||||||
chr12:113120410 | C | T | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.429-967G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120410 | ||||||
chr12:113120452 | C | T | 2 | a0002c0008t0005g0038a0002c0008t0005g0039 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.429-1009G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120452 | ||||||
chr12:113120471 | C | T | 13 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(10): Show | 14 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.429-1028G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120471 | ||||||
chr12:113120582 | C | G | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+927G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120582 | ||||||
chr12:113120840 | T | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.428+669A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120840 | ||||||
chr12:113120924 | G | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0098a0001c0001t0001g0145others(1): Show | 6 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+585C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120924 | ||||||
chr12:113121067 | T | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.428+442A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121067 | ||||||
chr12:113121084 | C | T | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.428+425G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121084 | ||||||
chr12:113121281 | C | T | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.428+228G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121281 | ||||||
chr12:113121322 | C | T | 1 | a0002c0019t0003g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.428+187G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121322 | ||||||
chr12:113121642 | A | G | 19 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(16): Show | 20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.299-4T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121642 | ||||||
chr12:113121726 | ATT | A | 10 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(7): Show | 11 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-90_299-89delAA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121726 | ||||||
chr12:113121777 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.299-139T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121777 | ||||||
chr12:113121800 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.299-162G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121800 | ||||||
chr12:113122065 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.299-427A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122065 | ||||||
chr12:113122227 | C | T | 14 | a0002c0002t0002g0007a0002c0002t0002g0012a0002c0002t0002g0013others(11): Show | 19 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-589G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122227 | ||||||
chr12:113122234 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299-596G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122234 | ||||||
chr12:113122426 | C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0129a0001c0001t0001g0142others(1): Show | 7 | HG00642.hp2 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-788G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122426 | ||||||
chr12:113122506 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-868C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122506 | ||||||
chr12:113122544 | C | T | 14 | a0002c0002t0002g0007a0002c0002t0002g0012a0002c0002t0002g0013others(11): Show | 19 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-906G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122544 | ||||||
chr12:113122569 | C | T | 1 | a0009c0014t0001g0091 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-931G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122569 | ||||||
chr12:113122574 | C | G | 2 | a0002c0003t0002g0071a0002c0003t0002g0073 | 2 | NA18951.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.299-936G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122574 | ||||||
chr12:113122601 | A | AGGCAGGA others(14): Show |
3 | a0002c0002t0003g0028a0002c0002t0006g0033a0002c0019t0003g0032 | 3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.299-984_299-964dup others(21): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122601 | ||||||
chr12:113122706 | A | T | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1068T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122706 | ||||||
chr12:113122841 | T | A | 15 | a0001c0001t0001g0025a0001c0001t0001g0101a0001c0001t0001g0107others(12): Show | 16 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-1203A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122841 | ||||||
chr12:113122850 | T | A | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.299-1212A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122850 | ||||||
chr12:113122966 | A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0190a0001c0001t0001g0214 | 3 | HG02630.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-1328T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122966 | ||||||
chr12:113123099 | C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.299-1461G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123099 | ||||||
chr12:113123144 | C | T | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-1506G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123144 | ||||||
chr12:113123189 | C | T | 1 | a0010c0012t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-1551G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123189 | ||||||
chr12:113123279 | A | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.299-1641T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123279 | ||||||
chr12:113123466 | C | T | 3 | a0002c0002t0003g0028a0002c0002t0006g0033a0002c0019t0003g0032 | 3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.299-1828G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123466 | ||||||
chr12:113123513 | G | A | 5 | a0002c0006t0004g0089a0002c0006t0004g0198a0002c0006t0004g0203others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1875C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123513 | ||||||
chr12:113123548 | CT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.299-1911delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123548 | ||||||
chr12:113123568 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-1930C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123568 | ||||||
chr12:113123708 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.299-2070G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123708 | ||||||
chr12:113123826 | G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(6): Show | 28 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.299-2188C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123826 | ||||||
chr12:113123923 | T | C | 3 | a0002c0002t0003g0028a0002c0002t0006g0033a0002c0019t0003g0032 | 3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.299-2285A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123923 | ||||||
chr12:113123926 | A | G | 15 | a0002c0002t0002g0007a0002c0002t0002g0012a0002c0002t0002g0013others(12): Show | 20 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-2288T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123926 | ||||||
chr12:113124090 | T | C | 23 | a0001c0001t0001g0037a0001c0001t0001g0059a0002c0002t0002g0007others(20): Show | 28 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.299-2452A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124090 | ||||||
chr12:113124133 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299-2495C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124133 | ||||||
chr12:113124174 | T | C | 1 | a0002c0003t0002g0077 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.299-2536A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124174 | ||||||
chr12:113124209 | C | A | 15 | a0002c0002t0002g0007a0002c0002t0002g0012a0002c0002t0002g0013others(12): Show | 20 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-2571G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124209 | ||||||
chr12:113124217 | C | CA | 9 | a0001c0001t0001g0205a0001c0001t0001g0238a0001c0001t0001g0239others(6): Show | 10 | HG01891.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-2580dupT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124217 | ||||||
chr12:113124217 | CA | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 159 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.299-2580delT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124217 | ||||||
chr12:113124217 | CAA | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(34): Show | 48 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.299-2581_299-2580d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124217 | ||||||
chr12:113124239 | A | AAT | 22 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0128others(19): Show | 27 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.299-2602_299-2601i others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124239 | ||||||
chr12:113124239 | A | AT | 11 | a0001c0001t0003g0029a0001c0001t0008g0031a0002c0002t0001g0020others(8): Show | 12 | HG00642.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-2602_299-2601i others(3): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124239 | ||||||
chr12:113124239 | A | T | 1 | a0002c0002t0001g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.299-2601T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124239 | ||||||
chr12:113124535 | C | A | 1 | a0001c0001t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-2897G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124535 | ||||||
chr12:113124670 | A | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0023others(19): Show | 29 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.299-3032T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124670 | ||||||
chr12:113124726 | T | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0003g0029 | 3 | HG01891.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.298+3086A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124726 | ||||||
chr12:113124745 | C | T | 2 | a0002c0002t0003g0028a0002c0002t0006g0033 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.298+3067G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124745 | ||||||
chr12:113124882 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.298+2930T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124882 | ||||||
chr12:113124895 | T | G | 1 | a0013c0023t0005g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+2917A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124895 | ||||||
chr12:113124916 | T | C | 2 | a0002c0008t0005g0038a0002c0008t0005g0039 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.298+2896A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124916 | ||||||
chr12:113125012 | G | A | 3 | a0002c0002t0002g0049a0002c0002t0002g0055a0002c0003t0002g0079 | 3 | NA18945.hp1 NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.298+2800C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125012 | ||||||
chr12:113125097 | T | TA | 36 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0065others(33): Show | 42 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(39): Show |
intron_variant | MODIFIER | c.298+2714dupT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125097 | ||||||
chr12:113125097 | TA | T | 24 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0129others(21): Show | 25 | HG00558.hp2 HG01071.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.298+2714delT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125097 | ||||||
chr12:113125122 | CAT | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0123a0001c0001t0001g0189 | 3 | NA18948.hp1 NA18954.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.298+2688_298+2689d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125122 | ||||||
chr12:113125167 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.298+2645C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125167 | ||||||
chr12:113125300 | C | T | 73 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0056others(70): Show | 83 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.298+2512G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125300 | ||||||
chr12:113125316 | G | A | 35 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0008g0031others(32): Show | 42 | HG00280.hp2 HG02040.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.298+2496C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125316 | ||||||
chr12:113125708 | G | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02056.hp2 NA18949.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.298+2104C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125708 | ||||||
chr12:113125762 | G | T | 28 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0008g0031others(25): Show | 34 | HG02040.hp2 HG02055.hp1 HG02080.hp2 others(31): Show |
intron_variant | MODIFIER | c.298+2050C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125762 | ||||||
chr12:113125947 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.298+1865T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125947 | ||||||
chr12:113126087 | C | A | 1 | a0002c0002t0002g0043 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.298+1725G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126087 | ||||||
chr12:113126111 | C | T | 1 | a0001c0001t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+1701G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126111 | ||||||
chr12:113126142 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.298+1670C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126142 | ||||||
chr12:113126182 | G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0140a0001c0001t0001g0157others(2): Show | 6 | HG01943.hp2 HG02572.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+1630C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126182 | ||||||
chr12:113126280 | G | A | 2 | a0002c0002t0003g0035a0002c0019t0003g0032 | 2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.298+1532C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126280 | ||||||
chr12:113126295 | A | T | 1 | a0002c0002t0006g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.298+1517T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126295 | ||||||
chr12:113126488 | G | A | 2 | a0002c0003t0002g0119a0002c0003t0002g0237 | 2 | NA18956.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.298+1324C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126488 | ||||||
chr12:113126688 | T | A | 1 | a0003c0010t0007g0027 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.298+1124A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | T | TCA | 27 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(24): Show | 44 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+1122_298+1123d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | T | TCACA | 10 | a0001c0001t0001g0151a0001c0001t0001g0190a0001c0001t0001g0191others(7): Show | 10 | HG00140.hp2 HG01891.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+1120_298+1123d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | T | TCACACA | 17 | a0001c0007t0001g0070a0001c0007t0001g0072a0002c0003t0001g0074others(14): Show | 18 | HG00438.hp2 HG02155.hp1 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+1118_298+1123d others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | T | TCACACAC others(1): Show |
4 | a0002c0003t0002g0080a0002c0003t0002g0081a0002c0003t0002g0084others(1): Show | 4 | HG02622.hp2 NA18954.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1116_298+1123d others(10): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | T | TCACACAC others(7): Show |
1 | a0001c0007t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.298+1110_298+1123d others(16): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | TCA | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0139a0001c0001t0001g0140others(8): Show | 12 | HG01943.hp2 HG02572.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+1122_298+1123d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | TCACA | T | 15 | a0001c0001t0001g0063a0001c0001t0001g0116a0001c0001t0001g0138others(12): Show | 16 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+1120_298+1123d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126688 | TCACACA | T | 17 | a0001c0001t0001g0050a0001c0001t0001g0056a0002c0002t0002g0007others(14): Show | 22 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.298+1118_298+1123d others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | ||||||
chr12:113126690 | A | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0004t0001g0014others(2): Show | 6 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+1122T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126690 | ||||||
chr12:113126692 | A | T | 3 | a0001c0004t0001g0014a0001c0004t0001g0062a0007c0026t0002g0046 | 4 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1120T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126692 | ||||||
chr12:113126694 | A | T | 9 | a0001c0001t0001g0063a0002c0002t0002g0026a0002c0002t0002g0047others(6): Show | 10 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+1118T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126694 | ||||||
chr12:113126696 | A | T | 13 | a0001c0001t0001g0050a0001c0001t0001g0056a0002c0002t0002g0007others(10): Show | 18 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+1116T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126696 | ||||||
chr12:113126698 | A | T | 2 | a0001c0001t0001g0050a0002c0018t0004g0040 | 2 | HG02080.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+1114T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126698 | ||||||
chr12:113126765 | A | C | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298+1047T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126765 | ||||||
chr12:113126769 | C | T | 4 | a0002c0002t0002g0026a0002c0002t0002g0243a0002c0002t0002g0244others(1): Show | 5 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1043G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126769 | ||||||
chr12:113126815 | T | C | 69 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0056others(66): Show | 78 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+997A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126815 | ||||||
chr12:113126928 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.298+884A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126928 | ||||||
chr12:113126944 | T | C | 3 | a0001c0004t0001g0014a0001c0004t0001g0062a0007c0026t0002g0046 | 4 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+868A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126944 | ||||||
chr12:113126950 | A | ATTATTAT others(25): Show |
29 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0008g0031others(26): Show | 35 | HG02040.hp2 HG02055.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.298+830_298+861dup others(32): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126950 | ||||||
chr12:113127067 | T | TAAATTAT others(38): Show |
1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.298+744_298+745ins others(45): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127067 | ||||||
chr12:113127069 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.298+743T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127069 | ||||||
chr12:113127070 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.298+742C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127070 | ||||||
chr12:113127119 | G | C | 28 | a0001c0001t0001g0050a0001c0001t0001g0056a0002c0002t0001g0020others(25): Show | 35 | HG02040.hp2 HG02055.hp2 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.298+693C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127119 | ||||||
chr12:113127267 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01099.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.298+545T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127267 | ||||||
chr12:113127430 | G | T | 33 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 35 | HG00438.hp2 HG00642.hp1 HG02071.hp2 others(32): Show |
intron_variant | MODIFIER | c.298+382C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127430 | ||||||
chr12:113127523 | A | C | 1 | a0002c0002t0001g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.298+289T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127523 | ||||||
chr12:113127527 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.298+285C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127527 | ||||||
chr12:113127543 | C | G | 35 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0008g0031others(32): Show | 42 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.298+269G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127543 | ||||||
chr12:113127578 | G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0101others(19): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.298+234C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127578 | ||||||
chr12:113127606 | C | T | 1 | a0004c0009t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.298+206G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127606 | ||||||
chr12:113127612 | C | T | 12 | a0001c0001t0008g0031a0001c0004t0001g0014a0001c0004t0001g0062others(9): Show | 13 | HG00280.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.298+200G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127612 | ||||||
chr12:113127735 | G | A | 8 | a0001c0001t0008g0031a0002c0002t0003g0028a0002c0002t0003g0035others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+77C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127735 | ||||||
chr12:113127918 | T | G | 1 | a0002c0003t0002g0066 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.237-45A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127918 | ||||||
chr12:113127919 | G | C | 1 | a0002c0003t0002g0066 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.237-46C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127919 | ||||||
chr12:113127923 | C | T | 1 | a0013c0023t0005g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.237-50G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127923 | ||||||
chr12:113127982 | G | C | 1 | a0002c0002t0001g0240 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.236+83C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127982 | ||||||
chr12:113127997 | C | T | 14 | a0001c0001t0001g0050a0001c0001t0001g0056a0002c0002t0002g0007others(11): Show | 19 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.236+68G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127997 | ||||||
chr12:113128245 | G | GAC | 32 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(29): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.123-69_123-68dupGT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | G | GACAC | 3 | a0001c0001t0001g0213a0002c0003t0002g0068a0002c0006t0004g0203 | 3 | HG00280.hp1 NA18747.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.123-71_123-68dupGT others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | G | GACACAC | 19 | a0001c0007t0001g0070a0001c0007t0001g0072a0002c0003t0001g0074others(16): Show | 20 | HG00438.hp2 HG02071.hp2 NA18945.hp2 others(17): Show |
intron_variant | MODIFIER | c.123-73_123-68dupGT others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | G | GACACACA others(1): Show |
3 | a0002c0003t0002g0082a0002c0003t0002g0085a0004c0009t0002g0036 | 3 | HG02155.hp1 HG02622.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.123-75_123-68dupGT others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | G | GACACACA others(3): Show |
1 | a0001c0007t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.123-77_123-68dupGT others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | G | GACACACA others(9): Show |
1 | a0001c0001t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-83_123-68dupGT others(14): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | GAC | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0017others(45): Show | 56 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.123-69_123-68delGT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | GACAC | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0095others(8): Show | 12 | HG00642.hp1 HG01358.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-71_123-68delGT others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | GACACAC | G | 3 | a0002c0008t0005g0038a0002c0008t0005g0039a0013c0023t0005g0120 | 3 | HG02572.hp2 HG03471.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.123-73_123-68delGT others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | GACACACA others(1): Show |
G | 26 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0008g0031others(23): Show | 32 | HG00280.hp2 HG02040.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.123-75_123-68delGT others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128245 | GACACACA others(5): Show |
G | 1 | a0007c0026t0002g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123-79_123-68delGT others(10): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | ||||||
chr12:113128282 | G | C | 1 | a0002c0003t0002g0084 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123-104C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128282 | ||||||
chr12:113128490 | A | AAC | 10 | a0001c0001t0001g0092a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG00741.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-314_123-313dup others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128490 | ||||||
chr12:113128512 | C | CACAG | 22 | a0001c0001t0001g0050a0001c0001t0001g0056a0002c0002t0002g0007others(19): Show | 28 | HG02040.hp2 HG02080.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.123-335_123-334ins others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128512 | ||||||
chr12:113128512 | C | G | 3 | a0002c0002t0006g0030a0002c0018t0004g0040a0003c0010t0007g0027 | 3 | HG00280.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.123-334G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128512 | ||||||
chr12:113128630 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.123-452G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128630 | ||||||
chr12:113128676 | C | T | 1 | a0003c0010t0007g0027 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123-498G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128676 | ||||||
chr12:113128712 | C | T | 2 | a0001c0001t0001g0104a0002c0002t0001g0240 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.123-534G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128712 | ||||||
chr12:113128839 | A | G | 1 | a0005c0024t0003g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.123-661T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128839 | ||||||
chr12:113128972 | G | GAC | 41 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0094others(38): Show | 46 | HG01168.hp1 HG01346.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.123-796_123-795dup others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | ||||||
chr12:113128972 | G | GACAC | 18 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0214others(15): Show | 20 | HG00642.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.123-798_123-795dup others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | ||||||
chr12:113128972 | G | GACACAC | 26 | a0001c0001t0001g0065a0001c0007t0001g0070a0001c0007t0001g0072others(23): Show | 28 | HG00438.hp2 HG02040.hp2 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-800_123-795dup others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | ||||||
chr12:113128972 | GAC | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 6 | HG02602.hp2 HG02647.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-796_123-795del others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | ||||||
chr12:113128972 | GACAC | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0005t0001g0221 | 3 | HG01099.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.123-798_123-795del others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | ||||||
chr12:113129067 | C | G | 1 | a0010c0012t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.123-889G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129067 | ||||||
chr12:113129124 | C | A | 14 | a0001c0001t0001g0050a0001c0001t0001g0056a0002c0002t0002g0007others(11): Show | 19 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.123-946G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129124 | ||||||
chr12:113129232 | C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0130 | 3 | HG01099.hp2 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.123-1054G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129232 | ||||||
chr12:113129361 | C | T | 1 | a0001c0001t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-1183G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129361 | ||||||
chr12:113129557 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+1328C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129557 | ||||||
chr12:113129713 | C | T | 1 | a0002c0002t0002g0219 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.122+1172G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129713 | ||||||
chr12:113129721 | C | T | 30 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0008g0031others(27): Show | 37 | HG02040.hp2 HG02055.hp1 HG02080.hp2 others(34): Show |
intron_variant | MODIFIER | c.122+1164G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129721 | ||||||
chr12:113129722 | G | A | 1 | a0005c0024t0003g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.122+1163C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129722 | ||||||
chr12:113129722 | G | GCACA | 3 | a0002c0008t0005g0038a0002c0008t0005g0039a0002c0018t0004g0040 | 3 | HG02572.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122+1159_122+1162d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129722 | ||||||
chr12:113129738 | A | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.122+1147T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129738 | ||||||
chr12:113130044 | G | A | 1 | a0002c0018t0004g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122+841C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130044 | ||||||
chr12:113130049 | G | T | 1 | a0013c0023t0005g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.122+836C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130049 | ||||||
chr12:113130094 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.122+791T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130094 | ||||||
chr12:113130253 | C | T | 1 | a0001c0022t0001g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.122+632G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130253 | ||||||
chr12:113130273 | T | G | 1 | a0001c0001t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+612A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130273 | ||||||
chr12:113130421 | C | A | 6 | a0001c0001t0008g0031a0002c0002t0003g0028a0002c0002t0003g0035others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+464G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130421 | ||||||
chr12:113130450 | T | G | 2 | a0001c0001t0001g0126a0003c0010t0007g0027 | 2 | HG00280.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.122+435A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130450 | ||||||
chr12:113130457 | G | A | 2 | a0001c0001t0003g0029a0002c0002t0006g0030 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.122+428C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130457 | ||||||
chr12:113130514 | C | G | 61 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0056others(58): Show | 70 | HG00438.hp2 HG00642.hp1 HG02040.hp2 others(67): Show |
intron_variant | MODIFIER | c.122+371G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130514 | ||||||
chr12:113130529 | A | G | 71 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0056others(68): Show | 80 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.122+356T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130529 | ||||||
chr12:113130536 | C | T | 3 | a0001c0001t0001g0126a0001c0001t0003g0029a0003c0010t0007g0027 | 3 | HG00280.hp2 HG01361.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.122+349G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130536 | ||||||
chr12:113130601 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.122+284C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130601 | ||||||
chr12:113130612 | G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 8 | HG00642.hp1 HG02148.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+273C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130612 | ||||||
chr12:113130690 | G | A | 1 | a0002c0002t0002g0236 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.122+195C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130690 | ||||||
chr12:113130772 | C | A | 16 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0002g0058others(13): Show | 21 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+113G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130772 | ||||||
chr12:113130943 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.66-2A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113130943 | ||||||
chr12:113130992 | A | G | 74 | a0001c0001t0001g0016a0001c0001t0001g0050a0001c0001t0001g0056others(71): Show | 83 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.66-51T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113130992 | ||||||
chr12:113131056 | C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02056.hp2 NA18949.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.66-115G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131056 | ||||||
chr12:113131100 | G | A | 1 | a0001c0005t0001g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.66-159C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131100 | ||||||
chr12:113131168 | A | G | 3 | a0002c0008t0005g0038a0002c0008t0005g0039a0002c0018t0004g0040 | 3 | HG02572.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.66-227T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131168 | ||||||
chr12:113131247 | T | G | 5 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.66-306A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131247 | ||||||
chr12:113131248 | G | T | 1 | a0001c0001t0001g0016 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.66-307C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131248 | ||||||
chr12:113131250 | G | C | 1 | a0001c0001t0001g0065 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.66-309C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131250 | ||||||
chr12:113131383 | G | A | 2 | a0002c0002t0001g0041a0002c0002t0001g0042 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.66-442C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131383 | ||||||
chr12:113131434 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.66-493G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131434 | ||||||
chr12:113131643 | T | C | 1 | a0001c0017t0001g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.66-702A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131643 | ||||||
chr12:113131857 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.66-916G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131857 | ||||||
chr12:113131932 | C | T | 13 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0107others(10): Show | 13 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.66-991G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131932 | ||||||
chr12:113131964 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.66-1023A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131964 | ||||||
chr12:113131968 | C | CT | 10 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0095others(7): Show | 11 | HG00642.hp1 HG00673.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.66-1028dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131968 | ||||||
chr12:113131968 | CT | C | 20 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(17): Show | 21 | HG00323.hp2 HG00408.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.66-1028delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131968 | ||||||
chr12:113131968 | CTT | C | 53 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0059others(50): Show | 59 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(56): Show |
intron_variant | MODIFIER | c.66-1029_66-1028del others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131968 | ||||||
chr12:113131983 | T | G | 1 | a0002c0003t0002g0237 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.66-1042A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131983 | ||||||
chr12:113132074 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.66-1133G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132074 | ||||||
chr12:113132239 | T | C | 62 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0059others(59): Show | 70 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.66-1298A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132239 | ||||||
chr12:113132269 | G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.66-1328C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132269 | ||||||
chr12:113132456 | C | A | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.66-1515G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132456 | ||||||
chr12:113132456 | C | T | 26 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0086others(23): Show | 27 | HG00408.hp2 HG00438.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.66-1515G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132456 | ||||||
chr12:113132457 | G | C | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.66-1516C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132457 | ||||||
chr12:113132524 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.66-1583G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132524 | ||||||
chr12:113132792 | C | A | 1 | a0002c0002t0001g0240 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.66-1851G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132792 | ||||||
chr12:113132879 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.66-1938G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132879 | ||||||
chr12:113132945 | C | T | 2 | a0001c0001t0001g0005a0009c0014t0001g0091 | 6 | HG02132.hp2 NA18956.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.66-2004G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132945 | ||||||
chr12:113133063 | G | A | 2 | a0001c0004t0001g0014a0001c0004t0001g0062 | 3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.66-2122C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133063 | ||||||
chr12:113133111 | C | T | 1 | a0003c0010t0007g0027 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.66-2170G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133111 | ||||||
chr12:113133379 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.65+2019G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133379 | ||||||
chr12:113133532 | T | C | 28 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0086others(25): Show | 29 | HG00408.hp2 HG00438.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.65+1866A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133532 | ||||||
chr12:113133564 | T | C | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1834A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133564 | ||||||
chr12:113133565 | C | T | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1833G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133565 | ||||||
chr12:113133568 | G | C | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1830C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133568 | ||||||
chr12:113133953 | C | G | 1 | a0002c0006t0004g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.65+1445G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133953 | ||||||
chr12:113134096 | AGGCCGTC others(10): Show |
A | 6 | a0001c0001t0008g0031a0002c0002t0003g0028a0002c0002t0003g0035others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.65+1285_65+1301del others(17): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134096 | ||||||
chr12:113134241 | T | G | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1157A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134241 | ||||||
chr12:113134250 | T | A | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1148A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134250 | ||||||
chr12:113134361 | A | G | 73 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0056others(70): Show | 81 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.65+1037T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134361 | ||||||
chr12:113134493 | G | A | 6 | a0002c0002t0002g0026a0002c0002t0002g0241a0002c0002t0002g0242others(3): Show | 7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.65+905C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134493 | ||||||
chr12:113134772 | G | C | 1 | a0001c0001t0001g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.65+626C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134772 | ||||||
chr12:113134846 | C | T | 1 | a0002c0002t0003g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65+552G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134846 | ||||||
chr12:113134929 | A | T | 1 | a0002c0002t0003g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65+469T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134929 | ||||||
chr12:113134930 | T | A | 1 | a0002c0002t0003g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65+468A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134930 | ||||||
chr12:113135059 | C | A | 1 | a0002c0002t0003g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65+339G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113135059 | ||||||
chr12:113135173 | C | T | 8 | a0001c0001t0003g0029a0001c0001t0008g0031a0002c0002t0003g0028others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.65+225G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113135173 |