geneid | 59339 |
---|---|
ensemblid | ENSG00000169499.15 |
hgncid | 14336 |
symbol | PLEKHA2 |
name | pleckstrin homology domain containing A2 |
refseq_nuc | NM_021623.2 |
refseq_prot | NP_067636.1 |
ensembl_nuc | ENST00000617275.5 |
ensembl_prot | ENSP00000482228.1 |
mane_status | MANE Select |
chr | chr8 |
start | 38901346 |
end | 38973912 |
strand | + |
ver | v1.2 |
region | chr8:38901346-38973912 |
region5000 | chr8:38896346-38978912 |
regionname0 | PLEKHA2_chr8_38901346_38973912 |
regionname5000 | PLEKHA2_chr8_38896346_38978912 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 425 | 368 | 88 | 69 | 154 | 16 | 39 | 116 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0002 | 0/0 | 425 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0003 | 0/0 | 425 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0004 | 0/0 | 425 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0005 | 0/0 | 425 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0006 | 0/0 | 425 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1278 | 365 | 87 | 68 | 153 | 16 | 39 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0002 | 0/0 | 1278 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0003 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0004 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0005 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0006 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0007 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0008 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
c0009 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4259 | 123 | 8 | 32 | 65 | 6 | 12 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0002 | 0/0 | 4254 | 66 | 11 | 14 | 29 | 6 | 6 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0003 | 0/1 | 4254 | 36 | 5 | 9 | 8 | 2 | 11 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0004 | 0/0 | 4255 | 16 | 1 | 1 | 13 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0005 | 0/0 | 4261 | 13 | 0 | 4 | 8 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0006 | 0/0 | 4253 | 9 | 0 | 3 | 6 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0007 | 0/0 | 4258 | 9 | 8 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0008 | 0/0 | 4257 | 7 | 1 | 1 | 4 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0009 | 0/0 | 4262 | 7 | 7 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0010 | 0/0 | 4259 | 6 | 0 | 0 | 6 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0011 | 1/0 | 4253 | 6 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0012 | 0/0 | 4253 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0013 | 0/0 | 4253 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0014 | 0/0 | 4253 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0015 | 0/0 | 4256 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0016 | 0/0 | 4262 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0017 | 0/0 | 4252 | 3 | 0 | 2 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0018 | 0/0 | 4263 | 3 | 1 | 0 | 2 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0019 | 0/0 | 4241 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0020 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0021 | 0/0 | 4253 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0022 | 0/0 | 4256 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0023 | 0/0 | 4261 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0024 | 0/0 | 4260 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0025 | 0/0 | 4262 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0026 | 0/0 | 4264 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0027 | 0/0 | 4252 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0028 | 0/0 | 4257 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0029 | 0/0 | 4260 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0030 | 0/0 | 4253 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0031 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0032 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0033 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0034 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0035 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0036 | 0/0 | 4255 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0037 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0038 | 0/0 | 4255 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0039 | 0/0 | 4256 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0040 | 0/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0041 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0042 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0043 | 0/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0044 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0045 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0046 | 0/0 | 4258 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0047 | 0/0 | 4258 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0048 | 0/0 | 4260 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0049 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0050 | 0/0 | 4241 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0051 | 0/0 | 4253 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0052 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0053 | 0/0 | 4255 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0054 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0055 | 0/0 | 4254 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0056 | 0/0 | 4254 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
t0057 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1278 | 365 | 87 | 68 | 153 | 16 | 39 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0003 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0007 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0008 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0002c0002 | 0/0 | 1278 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0003c0006 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0004c0004 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0005c0005 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0006c0009 | 0/0 | 1278 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5536 | 120 | 7 | 31 | 64 | 6 | 12 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0002 | 0/0 | 5531 | 65 | 11 | 13 | 29 | 6 | 6 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0003 | 0/1 | 5531 | 36 | 5 | 9 | 8 | 2 | 11 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0004 | 0/0 | 5532 | 15 | 0 | 1 | 13 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0005 | 0/0 | 5538 | 12 | 0 | 3 | 8 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0006 | 0/0 | 5530 | 9 | 0 | 3 | 6 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0007 | 0/0 | 5535 | 9 | 8 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0008 | 0/0 | 5534 | 6 | 1 | 1 | 4 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0009 | 0/0 | 5539 | 7 | 7 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0010 | 0/0 | 5536 | 6 | 0 | 0 | 6 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0011 | 1/0 | 5530 | 6 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0012 | 0/0 | 5530 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0013 | 0/0 | 5530 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0014 | 0/0 | 5530 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0015 | 0/0 | 5533 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0016 | 0/0 | 5539 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0017 | 0/0 | 5529 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0018 | 0/0 | 5540 | 3 | 1 | 0 | 2 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0019 | 0/0 | 5518 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0020 | 0/0 | 5519 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0021 | 0/0 | 5530 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0022 | 0/0 | 5533 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0023 | 0/0 | 5538 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0024 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0025 | 0/0 | 5539 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0026 | 0/0 | 5541 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0027 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0028 | 0/0 | 5534 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0029 | 0/0 | 5537 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0030 | 0/0 | 5530 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0032 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0033 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0034 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0035 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0036 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0037 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0038 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0039 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0040 | 0/0 | 5536 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0041 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0042 | 0/0 | 5535 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0043 | 0/0 | 5536 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0044 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0045 | 0/0 | 5535 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0046 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0047 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0048 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0049 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0050 | 0/0 | 5518 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0052 | 0/0 | 5531 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0053 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0054 | 0/0 | 5535 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0055 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0056 | 0/0 | 5531 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0001t0057 | 0/0 | 5531 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0003t0001 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0007t0016 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0001c0008t0017 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0002c0002t0001 | 0/0 | 5536 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0002c0002t0004 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0002c0002t0031 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0002c0002t0051 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0003c0006t0001 | 0/0 | 5536 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0004c0004t0005 | 0/0 | 5538 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0005c0005t0002 | 0/0 | 5531 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
a0006c0009t0008 | 0/0 | 5534 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | copy fasta | chr8 | 38896346 | 38978912 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0006g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0007g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0008g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0010g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0010g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0010g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0010g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0010g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0011g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0011g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0012g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0013g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0013g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0014g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0015g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0015g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0015g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0015g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0016g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0016g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0017g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0017g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0018g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0018g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0018g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0019g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0020g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0020g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0021g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0021g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0022g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0022g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0023g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0023g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0024g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0024g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0025g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0025g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0026g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0026g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0027g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0027g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0028g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0028g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0029g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0029g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0030g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0032g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0033g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0034g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0035g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0036g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0037g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0038g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0039g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0040g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0041g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0042g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0043g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0044g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0045g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0046g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0047g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0048g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0049g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0050g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0052g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0053g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0054g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0055g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0056g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0001t0057g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0007t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0001c0008t0017g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0002c0002t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0002c0002t0031g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0002c0002t0051g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0003c0006t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0004c0004t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0005c0005t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
a0006c0009t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0113 | EUR | GBR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00280 | hp2 | a0001 | c0001 | t0022 | g0222 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0060 | EUR | FIN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00609 | hp2 | a0001 | c0001 | t0010 | g0327 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00621 | hp2 | a0001 | c0001 | t0015 | g0240 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00673 | hp1 | a0001 | c0001 | t0052 | g0270 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00733 | hp1 | a0001 | c0001 | t0017 | g0194 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0301 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00735 | hp1 | a0001 | c0001 | t0056 | g0224 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01070 | hp1 | a0001 | c0001 | t0023 | g0359 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01071 | hp2 | a0001 | c0001 | t0023 | g0360 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0357 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01099 | hp2 | a0005 | c0005 | t0002 | g0338 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01168 | hp2 | a0004 | c0004 | t0005 | g0355 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01192 | hp1 | a0001 | c0001 | t0029 | g0003 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01243 | hp1 | a0001 | c0001 | t0022 | g0223 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01255 | hp1 | a0001 | c0001 | t0053 | g0005 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0366 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0365 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0348 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01515 | hp1 | a0001 | c0001 | t0042 | g0242 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0115 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01884 | hp1 | a0001 | c0001 | t0013 | g0121 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01891 | hp1 | a0001 | c0001 | t0013 | g0151 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0373 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0292 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0350 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0339 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01993 | hp1 | a0001 | c0008 | t0017 | g0370 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0356 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02027 | hp1 | a0001 | c0001 | t0015 | g0216 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02040 | hp2 | a0001 | c0001 | t0008 | g0088 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02055 | hp2 | a0001 | c0001 | t0020 | g0012 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02083 | hp2 | a0001 | c0001 | t0057 | g0226 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02132 | hp1 | a0001 | c0001 | t0010 | g0320 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02132 | hp2 | a0001 | c0001 | t0015 | g0334 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02135 | hp1 | a0001 | c0001 | t0046 | g0234 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02135 | hp2 | a0001 | c0003 | t0001 | g0306 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02145 | hp2 | a0001 | c0001 | t0029 | g0162 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02257 | hp1 | a0001 | c0001 | t0016 | g0132 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02257 | hp2 | a0001 | c0001 | t0024 | g0144 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02258 | hp1 | a0001 | c0001 | t0025 | g0125 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02258 | hp2 | a0001 | c0001 | t0035 | g0183 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0344 | AMR | PEL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02451 | hp1 | a0001 | c0001 | t0014 | g0179 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0145 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02622 | hp1 | a0001 | c0001 | t0016 | g0149 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0195 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02647 | hp1 | a0001 | c0001 | t0027 | g0153 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02647 | hp2 | a0001 | c0001 | t0037 | g0217 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02683 | hp1 | a0001 | c0001 | t0040 | g0266 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02717 | hp1 | a0001 | c0001 | t0024 | g0136 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02723 | hp1 | a0001 | c0001 | t0020 | g0126 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02723 | hp2 | a0002 | c0002 | t0031 | g0046 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02738 | hp1 | a0001 | c0001 | t0036 | g0305 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02738 | hp2 | a0006 | c0009 | t0008 | g0211 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02809 | hp1 | a0001 | c0001 | t0033 | g0207 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0128 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02818 | hp2 | a0001 | c0001 | t0050 | g0167 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02886 | hp1 | a0001 | c0001 | t0028 | g0155 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02895 | hp1 | a0002 | c0002 | t0051 | g0131 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02895 | hp2 | a0001 | c0001 | t0026 | g0137 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0129 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02896 | hp2 | a0001 | c0001 | t0018 | g0244 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02897 | hp1 | a0001 | c0001 | t0026 | g0135 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0130 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0120 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02922 | hp2 | a0001 | c0001 | t0014 | g0250 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03041 | hp1 | a0001 | c0001 | t0027 | g0165 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0150 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0182 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0249 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03130 | hp1 | a0001 | c0007 | t0016 | g0157 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0156 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0184 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03209 | hp2 | a0001 | c0001 | t0025 | g0013 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03239 | hp1 | a0001 | c0001 | t0038 | g0198 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0122 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03453 | hp2 | a0001 | c0001 | t0054 | g0160 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03486 | hp1 | a0001 | c0001 | t0012 | g0230 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0117 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03491 | hp2 | a0001 | c0001 | t0021 | g0186 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03516 | hp1 | a0001 | c0001 | t0019 | g0124 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03516 | hp2 | a0001 | c0001 | t0016 | g0004 | AFR | ESN | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0196 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0154 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0123 | AFR | MSL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03688 | hp1 | a0001 | c0001 | t0030 | g0018 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03688 | hp2 | a0001 | c0001 | t0039 | g0274 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0063 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03710 | hp2 | a0001 | c0001 | t0017 | g0061 | SAS | PJL | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0322 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | BEB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0028 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04204 | hp1 | a0001 | c0001 | t0043 | g0035 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18522 | hp1 | a0001 | c0001 | t0019 | g0143 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18522 | hp2 | a0001 | c0001 | t0013 | g0146 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0232 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18906 | hp1 | a0001 | c0001 | t0034 | g0181 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0367 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18944 | hp1 | a0001 | c0001 | t0018 | g0374 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18948 | hp1 | a0001 | c0001 | t0008 | g0340 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18948 | hp2 | a0001 | c0001 | t0021 | g0278 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18949 | hp1 | a0001 | c0001 | t0008 | g0288 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0361 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18953 | hp1 | a0001 | c0001 | t0047 | g0219 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0260 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18964 | hp1 | a0001 | c0001 | t0041 | g0319 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18964 | hp2 | a0001 | c0001 | t0015 | g0287 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18981 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18985 | hp2 | a0001 | c0001 | t0048 | g0317 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0352 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19006 | hp1 | a0001 | c0001 | t0010 | g0279 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0248 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0328 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19057 | hp2 | a0001 | c0001 | t0010 | g0261 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19060 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19063 | hp1 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19075 | hp1 | a0001 | c0001 | t0007 | g0300 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0351 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19085 | hp2 | a0001 | c0001 | t0044 | g0290 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19088 | hp2 | a0001 | c0001 | t0018 | g0095 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA19240 | hp2 | a0001 | c0001 | t0032 | g0101 | AFR | YRI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20129 | hp1 | a0001 | c0001 | t0055 | g0227 | AFR | ASW | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20129 | hp2 | a0001 | c0001 | t0049 | g0147 | AFR | ASW | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0206 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0092 | EUR | TSI | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0097 | SAS | GIH | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | GIH | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG01123 | hp2 | a0003 | c0006 | t0001 | g0050 | AMR | CLM | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0164 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0158 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0163 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG02559 | hp2 | a0001 | c0001 | t0045 | g0302 | AFR | ACB | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0200 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0152 | AFR | USA | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0166 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0299 | REF | REF | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0011 | g0159 | REF | REF | PLEKHA2_chr8_38896346_38978912 | PLEKHA2 | chr8 | 38896346 | 38978912 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38901443
|
G | GT | 1 | a0001 | 3 | HG00735.hp1 HG02083.hp2 NA20129.hp1 |
splice_region_variant | LOW | c.-26_-25insT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/12 | chr8 | 38901443 | ||||||
chr8:38936025
|
C | T | 1 | a0006 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.173C>T | p.Ala58Val | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/12 | 296/5530 | 173/1278 | 58/425 | chr8 | 38936025 | ||
chr8:38952236
|
T | A | 1 | a0002 | 4 | HG02723.hp2 HG02895.hp1 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.557T>A | p.Ile186Asn | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/12 | 680/5530 | 557/1278 | 186/425 | chr8 | 38952236 | ||
chr8:38952651
|
C | T | 1 | a0003 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.649C>T | p.Arg217Cys | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/12 | 772/5530 | 649/1278 | 217/425 | chr8 | 38952651 | ||
chr8:38957365
|
C | A | 1 | a0004 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.816C>A | p.Ser272Arg | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/12 | 939/5530 | 816/1278 | 272/425 | chr8 | 38957365 | ||
chr8:38969650
|
G | A | 1 | a0005 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1145G>A | p.Arg382His | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1268/5530 | 1145/1278 | 382/425 | chr8 | 38969650 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38950918
|
G | T | 1 | a0001c0008 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.414G>T | p.Leu138Leu | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/12 | 537/5530 | 414/1278 | 138/425 | chr8 | 38950918 | ||
chr8:38950981
|
C | G | 1 | a0001c0007 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.477C>G | p.Pro159Pro | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/12 | 600/5530 | 477/1278 | 159/425 | chr8 | 38950981 | ||
chr8:38952174
|
G | A | 1 | a0001c0003 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.495G>A | p.Gly165Gly | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/12 | 618/5530 | 495/1278 | 165/425 | chr8 | 38952174 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38969826
|
G | C | 1 | a0001c0001t0010 | 6 | HG00609.hp2 HG02132.hp1 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 43 | chr8 | 38969826 | |||||
chr8:38969834
|
G | A | 1 | a0001c0001t0049 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 51 | chr8 | 38969834 | |||||
chr8:38969941
|
C | CTG | 7 | a0001c0001t0008a0001c0001t0015a0001c0001t0022others(4): Show | 16 | HG00280.hp2 HG00621.hp2 HG01243.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*194_*195dupGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | ||||
chr8:38969941
|
C | CTGTG | 16 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(13): Show | 149 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*192_*195dupGTGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | ||||
chr8:38969941
|
C | CTGTGTG | 6 | a0001c0001t0005a0001c0001t0023a0001c0001t0024others(3): Show | 20 | HG00423.hp1 HG00733.hp2 HG01070.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*190_*195dupGTGTGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | ||||
chr8:38969941
|
C | CTGTGTGT others(1): Show |
5 | a0001c0001t0009a0001c0001t0016a0001c0001t0018others(2): Show | 16 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*188_*195dupGTGTGT others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | ||||
chr8:38969941
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0026 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186_*195dupGTGTGT others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 196 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | ||||
chr8:38969941
|
CTG | C | 6 | a0001c0001t0012a0001c0001t0014a0001c0001t0017others(3): Show | 15 | HG00733.hp1 HG01993.hp1 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*194_*195delGT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 194 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | ||||
chr8:38969941
|
CTGTGTGT others(5): Show |
C | 3 | a0001c0001t0019a0001c0001t0020a0001c0001t0050 | 5 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*184_*195delGTGTGT others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 184 | INFO_REALIGN_3_PRIME | chr8 | 38969941 | ||||
chr8:38970407
|
A | T | 4 | a0001c0001t0009a0001c0001t0024a0001c0001t0025others(1): Show | 13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*624A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 624 | chr8 | 38970407 | |||||
chr8:38970466
|
T | A | 2 | a0002c0002t0031a0002c0002t0051 | 2 | HG02723.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*683T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 683 | chr8 | 38970466 | |||||
chr8:38970570
|
G | T | 1 | a0001c0001t0014 | 4 | HG02451.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*787G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 787 | chr8 | 38970570 | |||||
chr8:38970595
|
G | A | 1 | a0001c0001t0040 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*812G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 812 | chr8 | 38970595 | |||||
chr8:38970615
|
G | A | 2 | a0001c0001t0032a0001c0001t0049 | 2 | NA19240.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*832G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 832 | chr8 | 38970615 | |||||
chr8:38970742
|
G | C | 1 | a0001c0001t0055 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 959 | chr8 | 38970742 | |||||
chr8:38970842
|
G | A | 1 | a0001c0001t0041 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1059 | chr8 | 38970842 | |||||
chr8:38971331
|
G | A | 1 | a0001c0001t0023 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1548G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1548 | chr8 | 38971331 | |||||
chr8:38971390
|
C | T | 1 | a0001c0001t0037 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1607 | chr8 | 38971390 | |||||
chr8:38971737
|
C | T | 3 | a0001c0001t0019a0001c0001t0020a0001c0001t0050 | 5 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1954C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1954 | chr8 | 38971737 | |||||
chr8:38971759
|
C | T | 3 | a0001c0001t0019a0001c0001t0020a0001c0001t0050 | 5 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 1976 | chr8 | 38971759 | |||||
chr8:38971844
|
G | A | 1 | a0001c0001t0033 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2061G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2061 | chr8 | 38971844 | |||||
chr8:38971850
|
G | C | 1 | a0001c0001t0037 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2067G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2067 | chr8 | 38971850 | |||||
chr8:38971878
|
C | T | 1 | a0001c0001t0036 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2095C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2095 | chr8 | 38971878 | |||||
chr8:38971879
|
G | A | 1 | a0001c0001t0054 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2096 | chr8 | 38971879 | |||||
chr8:38971946
|
C | CA | 26 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(23): Show | 194 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2173dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2174 | INFO_REALIGN_3_PRIME | chr8 | 38971946 | ||||
chr8:38972183
|
A | AT | 6 | a0001c0001t0012a0001c0001t0014a0001c0001t0027others(3): Show | 14 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2412dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2413 | INFO_REALIGN_3_PRIME | chr8 | 38972183 | ||||
chr8:38972183
|
AT | A | 4 | a0001c0001t0019a0001c0001t0021a0001c0001t0038others(1): Show | 6 | HG01515.hp1 HG03239.hp1 HG03491.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2412delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2412 | INFO_REALIGN_3_PRIME | chr8 | 38972183 | ||||
chr8:38972349
|
G | T | 2 | a0001c0001t0028a0001c0001t0034 | 3 | HG02886.hp1 HG03579.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2566G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2566 | chr8 | 38972349 | |||||
chr8:38972422
|
T | C | 1 | a0001c0001t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2639T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2639 | chr8 | 38972422 | |||||
chr8:38972486
|
GA | G | 1 | a0001c0001t0006 | 9 | HG01928.hp2 HG01981.hp1 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2705delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2705 | INFO_REALIGN_3_PRIME | chr8 | 38972486 | ||||
chr8:38972530
|
A | G | 27 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(24): Show | 195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2747A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2747 | chr8 | 38972530 | |||||
chr8:38972531
|
A | G | 27 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(24): Show | 195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2748A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2748 | chr8 | 38972531 | |||||
chr8:38972565
|
T | C | 1 | a0001c0001t0043 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2782T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2782 | chr8 | 38972565 | |||||
chr8:38972772
|
T | G | 2 | a0001c0001t0039a0001c0001t0049 | 2 | HG03688.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2989T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 2989 | chr8 | 38972772 | |||||
chr8:38972814
|
T | G | 1 | a0001c0001t0025 | 2 | HG02258.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3031T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3031 | chr8 | 38972814 | |||||
chr8:38972887
|
A | T | 1 | a0001c0001t0044 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3104A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3104 | chr8 | 38972887 | |||||
chr8:38973540
|
A | G | 47 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(44): Show | 267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*3757A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3757 | chr8 | 38973540 | |||||
chr8:38973615
|
T | C | 4 | a0001c0001t0009a0001c0001t0024a0001c0001t0025others(1): Show | 13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3832T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 12/12 | 3832 | chr8 | 38973615 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38901439
|
C | CG | 335 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(332): Show | 337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
splice_donor_variant&intron_variant | HIGH | c.-24+1dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38901439 | |||||
chr8:38901499
|
GGGGGCTG others(17): Show |
G | 1 | a0001c0001t0018g0374 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-24+59_-24+82delCT others(22): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38901499 | |||||
chr8:38901524
|
G | A | 3 | a0001c0001t0016g0004a0001c0001t0029g0003a0001c0001t0053g0005 | 3 | HG01192.hp1 HG01255.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+79G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901524 | ||||||
chr8:38901710
|
C | T | 72 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0311others(69): Show | 73 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-24+265C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901710 | ||||||
chr8:38901730
|
C | CG | 10 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0002g0007others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+291dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38901730 | |||||
chr8:38901745
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0177a0001c0001t0001g0185others(204): Show | 209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.-24+300C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901745 | ||||||
chr8:38901890
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-24+445C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901890 | ||||||
chr8:38901951
|
C | T | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-24+506C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38901951 | ||||||
chr8:38902074
|
G | C | 55 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(52): Show | 55 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-24+629G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902074 | ||||||
chr8:38902092
|
C | A | 72 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0311others(69): Show | 73 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-24+647C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902092 | ||||||
chr8:38902130
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA18982.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-24+685C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902130 | ||||||
chr8:38902145
|
C | T | 1 | a0001c0001t0005g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24+700C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902145 | ||||||
chr8:38902203
|
A | C | 1 | a0001c0001t0007g0300 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-24+758A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902203 | ||||||
chr8:38902216
|
GGT | G | 16 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0229others(13): Show | 16 | HG02257.hp2 HG02451.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-24+775_-24+776del others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902216 | |||||
chr8:38902218
|
T | TG | 49 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0047others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.-24+774dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | |||||
chr8:38902218
|
T | TGG | 33 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0029others(30): Show | 33 | HG00280.hp1 HG00639.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-24+774_-24+775ins others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | |||||
chr8:38902218
|
T | TGGG | 24 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(21): Show | 24 | HG01358.hp1 HG01516.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24+774_-24+775ins others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | |||||
chr8:38902218
|
T | TGGGG | 11 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(8): Show | 11 | HG00423.hp2 HG03540.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+774_-24+775ins others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38902218 | |||||
chr8:38902219
|
GT | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0127others(45): Show | 48 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-24+775delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902219 | ||||||
chr8:38902220
|
T | G | 218 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-24+775T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902220 | ||||||
chr8:38902221
|
G | C | 4 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0010g0232others(1): Show | 4 | HG02135.hp1 NA18612.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+776G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902221 | ||||||
chr8:38902222
|
G | C | 28 | a0001c0001t0001g0177a0001c0001t0001g0185a0001c0001t0001g0188others(25): Show | 28 | HG00733.hp1 HG00738.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-24+777G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902222 | ||||||
chr8:38902233
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0008g0196a0001c0001t0032g0101 | 3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+788T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902233 | ||||||
chr8:38902387
|
G | A | 47 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-24+942G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902387 | ||||||
chr8:38902406
|
A | G | 1 | a0001c0001t0001g0371 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-24+961A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902406 | ||||||
chr8:38902501
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-24+1056G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902501 | ||||||
chr8:38902507
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-24+1062G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902507 | ||||||
chr8:38902516
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0002g0228a0001c0001t0012g0195others(1): Show | 4 | HG00733.hp1 HG02630.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+1071C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902516 | ||||||
chr8:38902529
|
A | G | 61 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(58): Show | 61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-24+1084A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902529 | ||||||
chr8:38902614
|
C | A | 223 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(220): Show | 224 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.-24+1169C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902614 | ||||||
chr8:38902731
|
A | G | 3 | a0001c0001t0001g0298a0001c0001t0003g0297a0001c0001t0003g0299 | 3 | HG00741.hp1 HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-24+1286A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902731 | ||||||
chr8:38902933
|
C | T | 3 | a0001c0001t0001g0294a0001c0001t0001g0296a0001c0001t0004g0295 | 3 | HG02015.hp2 HG02083.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-24+1488C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38902933 | ||||||
chr8:38903076
|
A | G | 25 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0213others(22): Show | 25 | HG00280.hp2 HG00735.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-24+1631A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903076 | ||||||
chr8:38903216
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-24+1771A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903216 | ||||||
chr8:38903494
|
G | A | 8 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0212others(5): Show | 8 | HG01123.hp1 HG01168.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+2049G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903494 | ||||||
chr8:38903577
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-24+2132A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903577 | ||||||
chr8:38903617
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0008g0196a0001c0001t0032g0101 | 3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+2172A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903617 | ||||||
chr8:38903665
|
C | G | 49 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0098others(46): Show | 49 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-24+2220C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903665 | ||||||
chr8:38903708
|
G | A | 3 | a0001c0001t0016g0004a0001c0001t0029g0003a0001c0001t0053g0005 | 3 | HG01192.hp1 HG01255.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+2263G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38903708 | ||||||
chr8:38904098
|
G | C | 11 | a0001c0001t0007g0122a0001c0001t0007g0129a0001c0001t0007g0130others(8): Show | 11 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+2653G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904098 | ||||||
chr8:38904133
|
C | T | 1 | a0001c0001t0011g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+2688C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904133 | ||||||
chr8:38904287
|
G | T | 144 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0177others(141): Show | 145 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.-24+2842G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904287 | ||||||
chr8:38904323
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-24+2878G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904323 | ||||||
chr8:38904334
|
G | T | 100 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-24+2889G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904334 | ||||||
chr8:38904425
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-24+2980T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904425 | ||||||
chr8:38904538
|
A | G | 100 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-24+3093A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904538 | ||||||
chr8:38904671
|
T | C | 47 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-24+3226T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904671 | ||||||
chr8:38904728
|
G | A | 2 | a0001c0001t0003g0171a0001c0001t0003g0172 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-24+3283G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904728 | ||||||
chr8:38904791
|
C | G | 2 | a0001c0001t0049g0147a0001c0001t0050g0167 | 2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+3346C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904791 | ||||||
chr8:38904837
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-24+3392A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904837 | ||||||
chr8:38904966
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-24+3521T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38904966 | ||||||
chr8:38905017
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-24+3572C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905017 | ||||||
chr8:38905228
|
G | T | 1 | a0001c0001t0002g0014 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-24+3783G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905228 | ||||||
chr8:38905352
|
G | A | 2 | a0001c0001t0002g0201a0001c0001t0009g0200 | 2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-24+3907G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905352 | ||||||
chr8:38905412
|
C | T | 1 | a0001c0001t0002g0369 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-24+3967C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905412 | ||||||
chr8:38905458
|
TA | T | 284 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(281): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-24+4025delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38905458 | |||||
chr8:38905599
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-24+4154G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905599 | ||||||
chr8:38905661
|
G | C | 1 | a0001c0001t0036g0305 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-24+4216G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905661 | ||||||
chr8:38905685
|
C | CT | 240 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-24+4257dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38905685 | |||||
chr8:38905685
|
C | CTT | 9 | a0001c0001t0001g0064a0001c0001t0001g0127a0001c0001t0001g0368others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-24+4256_-24+4257d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38905685 | |||||
chr8:38905715
|
C | T | 1 | a0001c0001t0012g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-24+4270C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905715 | ||||||
chr8:38905729
|
T | G | 289 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-24+4284T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905729 | ||||||
chr8:38905753
|
C | T | 3 | a0001c0001t0016g0004a0001c0001t0029g0003a0001c0001t0053g0005 | 3 | HG01192.hp1 HG01255.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+4308C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905753 | ||||||
chr8:38905789
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-24+4344A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905789 | ||||||
chr8:38905802
|
A | G | 1 | a0001c0001t0017g0194 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-24+4357A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905802 | ||||||
chr8:38905882
|
C | T | 9 | a0001c0001t0001g0316a0001c0001t0001g0363a0001c0001t0001g0364others(6): Show | 9 | HG01257.hp1 HG01258.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24+4437C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38905882 | ||||||
chr8:38906089
|
G | A | 53 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(50): Show | 53 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-24+4644G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906089 | ||||||
chr8:38906150
|
G | T | 11 | a0001c0001t0007g0122a0001c0001t0007g0129a0001c0001t0007g0130others(8): Show | 11 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+4705G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906150 | ||||||
chr8:38906198
|
C | T | 143 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0177others(140): Show | 144 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.-24+4753C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906198 | ||||||
chr8:38906207
|
A | C | 1 | a0001c0001t0008g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-24+4762A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906207 | ||||||
chr8:38906261
|
T | C | 46 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.-24+4816T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906261 | ||||||
chr8:38906465
|
C | A | 3 | a0001c0001t0001g0100a0001c0001t0008g0196a0001c0001t0032g0101 | 3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+5020C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906465 | ||||||
chr8:38906853
|
G | A | 1 | a0001c0001t0011g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-24+5408G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906853 | ||||||
chr8:38906857
|
A | G | 1 | a0001c0001t0005g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24+5412A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906857 | ||||||
chr8:38906974
|
C | G | 3 | a0001c0001t0012g0182a0001c0001t0012g0184a0001c0001t0035g0183 | 3 | HG02258.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-24+5529C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38906974 | ||||||
chr8:38907206
|
A | G | 4 | a0001c0001t0001g0213a0001c0001t0002g0212a0001c0001t0003g0210others(1): Show | 4 | HG01168.hp1 HG01256.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+5761A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907206 | ||||||
chr8:38907211
|
T | C | 1 | a0001c0001t0038g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-24+5766T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907211 | ||||||
chr8:38907322
|
ATTAT | A | 3 | a0001c0001t0001g0241a0001c0001t0002g0243a0001c0001t0042g0242 | 3 | HG00735.hp2 HG01069.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-24+5882_-24+5885d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907322 | |||||
chr8:38907424
|
G | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0204a0001c0001t0001g0205others(23): Show | 26 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.-24+5979G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907424 | ||||||
chr8:38907608
|
A | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0127others(24): Show | 27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-24+6163A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907608 | ||||||
chr8:38907675
|
C | A | 11 | a0001c0001t0007g0122a0001c0001t0007g0129a0001c0001t0007g0130others(8): Show | 11 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+6230C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907675 | ||||||
chr8:38907760
|
C | CA | 243 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-24+6330dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907760 | |||||
chr8:38907760
|
C | CAA | 113 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0083others(110): Show | 114 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-24+6329_-24+6330d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907760 | |||||
chr8:38907780
|
T | A | 8 | a0001c0001t0007g0122a0001c0001t0007g0129a0001c0001t0007g0130others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+6335T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907780 | ||||||
chr8:38907796
|
C | T | 7 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0014others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24+6351C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38907796 | ||||||
chr8:38907818
|
T | TTATG | 143 | a0001c0001t0001g0038a0001c0001t0001g0073a0001c0001t0001g0077others(140): Show | 144 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-24+6417_-24+6420d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | |||||
chr8:38907818
|
T | TTATGTAT others(1): Show |
4 | a0001c0001t0002g0079a0001c0001t0002g0321a0001c0001t0002g0322others(1): Show | 4 | HG00673.hp2 HG03831.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+6413_-24+6420d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | |||||
chr8:38907818
|
TTATG | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0236a0001c0001t0001g0241others(8): Show | 12 | HG00735.hp2 HG01069.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.-24+6417_-24+6420d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | |||||
chr8:38907818
|
TTATGTAT others(1): Show |
T | 5 | a0001c0001t0001g0043a0001c0001t0001g0291a0001c0001t0002g0041others(2): Show | 5 | HG02056.hp1 HG02486.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+6413_-24+6420d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | |||||
chr8:38907818
|
TTATGTAT others(5): Show |
T | 46 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(43): Show | 46 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-24+6409_-24+6420d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38907818 | |||||
chr8:38908114
|
C | A | 6 | a0001c0001t0007g0148a0001c0001t0007g0150a0001c0001t0013g0151others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+6669C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908114 | ||||||
chr8:38908237
|
C | A | 6 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221others(3): Show | 6 | HG02027.hp1 HG02165.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+6792C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908237 | ||||||
chr8:38908388
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0003g0042 | 2 | HG02486.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-24+6943G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908388 | ||||||
chr8:38908556
|
A | G | 48 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0177others(45): Show | 48 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.-24+7111A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908556 | ||||||
chr8:38908671
|
C | T | 1 | a0001c0001t0003g0299 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-24+7226C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908671 | ||||||
chr8:38908929
|
T | G | 280 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-24+7484T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38908929 | ||||||
chr8:38909073
|
G | A | 118 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0177others(115): Show | 119 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.-24+7628G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909073 | ||||||
chr8:38909142
|
C | CA | 7 | a0001c0001t0001g0084a0001c0001t0001g0251a0001c0001t0001g0252others(4): Show | 7 | NA18973.hp2 NA18985.hp1 NA19030.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+7711dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909142 | |||||
chr8:38909142
|
CA | C | 78 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-24+7711delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909142 | |||||
chr8:38909335
|
G | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0127others(24): Show | 27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-24+7890G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909335 | ||||||
chr8:38909393
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-24+7948A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909393 | ||||||
chr8:38909453
|
C | T | 1 | a0001c0001t0005g0357 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-24+8008C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909453 | ||||||
chr8:38909467
|
A | AG | 281 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(278): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-24+8022_-24+8023i others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909467 | ||||||
chr8:38909493
|
G | C | 2 | a0001c0001t0002g0112a0001c0001t0002g0115 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-24+8048G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909493 | ||||||
chr8:38909532
|
T | C | 5 | a0001c0001t0001g0083a0001c0001t0001g0363a0001c0001t0002g0082others(2): Show | 5 | NA18951.hp1 NA18957.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+8087T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909532 | ||||||
chr8:38909586
|
T | C | 1 | a0001c0001t0037g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-24+8141T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909586 | ||||||
chr8:38909925
|
C | T | 4 | a0001c0001t0001g0314a0001c0001t0002g0318a0001c0001t0002g0348others(1): Show | 4 | HG01361.hp2 HG01496.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-7982C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38909925 | ||||||
chr8:38909959
|
C | CT | 121 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0083others(118): Show | 122 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(119): Show |
intron_variant | MODIFIER | c.-23-7933dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909959 | |||||
chr8:38909959
|
C | CTT | 6 | a0001c0001t0001g0313a0001c0001t0001g0346a0001c0001t0002g0347others(3): Show | 6 | HG00423.hp1 HG02132.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-7934_-23-7933d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38909959 | |||||
chr8:38910216
|
C | T | 2 | a0001c0001t0002g0109a0001c0001t0018g0095 | 2 | NA18982.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-23-7691C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910216 | ||||||
chr8:38910266
|
G | T | 285 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(282): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-23-7641G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910266 | ||||||
chr8:38910561
|
G | A | 4 | a0001c0001t0001g0314a0001c0001t0002g0318a0001c0001t0002g0348others(1): Show | 4 | HG01361.hp2 HG01496.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-7346G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910561 | ||||||
chr8:38910916
|
G | A | 40 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-6991G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38910916 | ||||||
chr8:38911049
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-23-6858G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911049 | ||||||
chr8:38911170
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-23-6737C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911170 | ||||||
chr8:38911171
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-23-6736G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911171 | ||||||
chr8:38911244
|
C | CT | 221 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0022others(218): Show | 222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-23-6653dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38911244 | |||||
chr8:38911298
|
A | G | 224 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0022others(221): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-23-6609A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911298 | ||||||
chr8:38911636
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-23-6271G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38911636 | ||||||
chr8:38912038
|
C | T | 1 | a0001c0001t0021g0278 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-23-5869C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912038 | ||||||
chr8:38912475
|
C | T | 1 | a0001c0001t0002g0345 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-23-5432C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912475 | ||||||
chr8:38912534
|
C | T | 1 | a0001c0001t0019g0143 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-23-5373C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912534 | ||||||
chr8:38912606
|
A | G | 1 | a0001c0001t0003g0277 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-23-5301A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912606 | ||||||
chr8:38912690
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-23-5217G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38912690 | ||||||
chr8:38913295
|
C | T | 39 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.-23-4612C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913295 | ||||||
chr8:38913370
|
G | GA | 283 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-23-4521dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38913370 | |||||
chr8:38913370
|
G | GAA | 6 | a0001c0001t0001g0016a0001c0001t0001g0110a0001c0001t0007g0130others(3): Show | 6 | HG02129.hp2 HG02897.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-4522_-23-4521d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38913370 | |||||
chr8:38913379
|
A | AG | 3 | a0001c0001t0003g0060a0001c0001t0005g0063a0001c0001t0043g0035 | 3 | HG00323.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-23-4528_-23-4527i others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913379 | ||||||
chr8:38913396
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-23-4511A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913396 | ||||||
chr8:38913469
|
A | G | 291 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-23-4438A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913469 | ||||||
chr8:38913497
|
A | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0127others(24): Show | 27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-23-4410A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913497 | ||||||
chr8:38913742
|
TC | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0002g0033others(5): Show | 8 | HG02015.hp1 HG02155.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23-4160delC | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38913742 | |||||
chr8:38913748
|
G | A | 1 | a0001c0001t0007g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-23-4159G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913748 | ||||||
chr8:38913890
|
A | G | 291 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-23-4017A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913890 | ||||||
chr8:38913968
|
T | C | 27 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0127others(24): Show | 27 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-23-3939T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913968 | ||||||
chr8:38913985
|
G | T | 1 | a0001c0001t0003g0349 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-23-3922G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38913985 | ||||||
chr8:38914063
|
G | A | 291 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-23-3844G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914063 | ||||||
chr8:38914247
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-23-3660G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914247 | ||||||
chr8:38914644
|
A | C | 289 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-3263A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914644 | ||||||
chr8:38914731
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0008g0196a0001c0001t0032g0101 | 3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-23-3176T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914731 | ||||||
chr8:38914883
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-23-3024C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914883 | ||||||
chr8:38914953
|
A | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0003g0080others(1): Show | 4 | HG00423.hp2 NA19005.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-2954A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38914953 | ||||||
chr8:38914957
|
CTCT | C | 81 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0081others(78): Show | 81 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-23-2943_-23-2941d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 38914957 | |||||
chr8:38915038
|
T | C | 289 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2869T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915038 | ||||||
chr8:38915100
|
G | A | 289 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2807G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915100 | ||||||
chr8:38915168
|
A | G | 7 | a0001c0001t0001g0197a0001c0001t0002g0228a0001c0001t0014g0248others(4): Show | 7 | HG00733.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-2739A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915168 | ||||||
chr8:38915183
|
C | T | 51 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0177others(48): Show | 51 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-23-2724C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915183 | ||||||
chr8:38915202
|
C | T | 289 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2705C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915202 | ||||||
chr8:38915370
|
G | T | 26 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0127others(23): Show | 26 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23-2537G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915370 | ||||||
chr8:38915462
|
C | T | 26 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0127others(23): Show | 26 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23-2445C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915462 | ||||||
chr8:38915695
|
T | G | 1 | a0001c0001t0002g0245 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-23-2212T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915695 | ||||||
chr8:38915709
|
C | A | 59 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(56): Show | 59 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-23-2198C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915709 | ||||||
chr8:38915711
|
G | A | 6 | a0001c0001t0007g0122a0001c0001t0007g0129a0001c0001t0007g0130others(3): Show | 6 | HG02257.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-2196G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915711 | ||||||
chr8:38915746
|
T | C | 289 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-23-2161T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915746 | ||||||
chr8:38915830
|
T | G | 2 | a0001c0001t0001g0325a0001c0001t0002g0324 | 2 | NA18943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-23-2077T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915830 | ||||||
chr8:38915873
|
T | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(53): Show | 56 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-23-2034T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915873 | ||||||
chr8:38915922
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0002g0074a0001c0001t0002g0079others(2): Show | 5 | NA18941.hp1 NA18944.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-1985T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915922 | ||||||
chr8:38915937
|
C | G | 3 | a0001c0001t0001g0127a0001c0001t0020g0126a0002c0002t0004g0123 | 3 | HG02055.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-23-1970C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38915937 | ||||||
chr8:38916034
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-23-1873G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916034 | ||||||
chr8:38916138
|
G | A | 1 | a0001c0001t0037g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-23-1769G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916138 | ||||||
chr8:38916255
|
G | T | 5 | a0001c0001t0001g0073a0001c0001t0002g0074a0001c0001t0002g0079others(2): Show | 5 | NA18941.hp1 NA18944.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-1652G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916255 | ||||||
chr8:38916376
|
T | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(13): Show | 16 | HG00423.hp2 HG02040.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23-1531T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916376 | ||||||
chr8:38916482
|
A | G | 1 | a0001c0001t0006g0344 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-23-1425A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916482 | ||||||
chr8:38916554
|
C | T | 1 | a0001c0001t0050g0167 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-23-1353C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916554 | ||||||
chr8:38916841
|
T | C | 296 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-23-1066T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916841 | ||||||
chr8:38916934
|
G | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0068others(1): Show | 4 | HG02080.hp2 HG02129.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-973G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38916934 | ||||||
chr8:38917178
|
C | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0213a0001c0001t0001g0214others(6): Show | 9 | HG00280.hp2 HG00639.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23-729C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917178 | ||||||
chr8:38917178
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-23-729C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917178 | ||||||
chr8:38917288
|
C | T | 65 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23-619C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917288 | ||||||
chr8:38917423
|
C | T | 1 | a0001c0001t0001g0343 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-23-484C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917423 | ||||||
chr8:38917675
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-23-232A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 1/11 | chr8 | 38917675 | ||||||
chr8:38918282
|
C | T | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.141+212C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918282 | ||||||
chr8:38918312
|
C | G | 40 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.141+242C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918312 | ||||||
chr8:38918423
|
C | G | 373 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(370): Show | 375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.141+353C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918423 | ||||||
chr8:38918474
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.141+404C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918474 | ||||||
chr8:38918553
|
C | CACACAAA others(190): Show |
1 | a0001c0001t0013g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | |||||
chr8:38918553
|
C | CACACAAA others(190): Show |
1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | |||||
chr8:38918553
|
C | CACACAAA others(179): Show |
2 | a0001c0001t0005g0350a0001c0001t0028g0154 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+488_141+489ins others(186): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | |||||
chr8:38918553
|
C | CACACAAA others(190): Show |
324 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | |||||
chr8:38918553
|
C | CACACAAA others(190): Show |
1 | a0001c0001t0049g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | |||||
chr8:38918553
|
C | CACACAAA others(190): Show |
40 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | |||||
chr8:38918553
|
C | CACACAAA others(190): Show |
1 | a0001c0001t0017g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918553 | |||||
chr8:38918556
|
A | ACAAACAC others(190): Show |
3 | a0001c0001t0007g0148a0001c0001t0007g0150a0001c0001t0013g0151 | 3 | HG01891.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.141+488_141+489ins others(197): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38918556 | |||||
chr8:38918561
|
T | C | 2 | a0001c0001t0005g0350a0001c0001t0028g0154 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+491T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918561 | ||||||
chr8:38918562
|
T | C | 2 | a0001c0001t0005g0350a0001c0001t0028g0154 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+492T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918562 | ||||||
chr8:38918564
|
T | G | 2 | a0001c0001t0005g0350a0001c0001t0028g0154 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+494T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918564 | ||||||
chr8:38918572
|
C | T | 2 | a0001c0001t0005g0350a0001c0001t0028g0154 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+502C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918572 | ||||||
chr8:38918575
|
G | A | 2 | a0001c0001t0005g0350a0001c0001t0028g0154 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.141+505G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918575 | ||||||
chr8:38918646
|
A | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | NA18946.hp1 NA18946.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+576A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918646 | ||||||
chr8:38918679
|
C | A | 6 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221others(3): Show | 6 | HG02027.hp1 HG02165.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+609C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918679 | ||||||
chr8:38918681
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0008g0196a0001c0001t0032g0101 | 3 | HG01891.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.141+611C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918681 | ||||||
chr8:38918685
|
G | A | 8 | a0001c0001t0001g0177a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 8 | HG00733.hp2 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+615G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918685 | ||||||
chr8:38918707
|
G | A | 1 | a0001c0001t0053g0005 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+637G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918707 | ||||||
chr8:38918738
|
G | A | 2 | a0001c0001t0019g0124a0001c0001t0025g0125 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.141+668G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918738 | ||||||
chr8:38918743
|
C | T | 3 | a0001c0001t0012g0182a0001c0001t0012g0184a0001c0001t0035g0183 | 3 | HG02258.hp2 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.141+673C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918743 | ||||||
chr8:38918744
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141+674G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918744 | ||||||
chr8:38918746
|
A | G | 1 | a0001c0001t0008g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.141+676A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918746 | ||||||
chr8:38918892
|
T | C | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+822T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918892 | ||||||
chr8:38918905
|
C | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(291): Show | 295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.141+835C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918905 | ||||||
chr8:38918957
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.141+887C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38918957 | ||||||
chr8:38919090
|
T | G | 1 | a0001c0001t0033g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141+1020T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919090 | ||||||
chr8:38919120
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.141+1050G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919120 | ||||||
chr8:38919395
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(160): Show | 164 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(161): Show |
intron_variant | MODIFIER | c.141+1325T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919395 | ||||||
chr8:38919628
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(158): Show | 162 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.141+1558G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919628 | ||||||
chr8:38919831
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.141+1761A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919831 | ||||||
chr8:38919942
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.141+1872G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38919942 | ||||||
chr8:38920118
|
T | A | 1 | a0001c0001t0053g0005 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+2048T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920118 | ||||||
chr8:38920133
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.141+2063G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920133 | ||||||
chr8:38920182
|
T | G | 1 | a0001c0001t0021g0278 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.141+2112T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920182 | ||||||
chr8:38920199
|
A | G | 4 | a0001c0001t0003g0134a0001c0001t0003g0141a0001c0001t0009g0142others(1): Show | 4 | HG02451.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+2129A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920199 | ||||||
chr8:38920211
|
C | T | 1 | a0001c0001t0005g0063 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.141+2141C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920211 | ||||||
chr8:38920225
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0019others(179): Show | 183 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.141+2155G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920225 | ||||||
chr8:38920236
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.141+2166T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920236 | ||||||
chr8:38920296
|
A | G | 46 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.141+2226A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920296 | ||||||
chr8:38920308
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.141+2238G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920308 | ||||||
chr8:38920355
|
T | C | 28 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0054others(25): Show | 28 | HG00408.hp2 HG01175.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.141+2285T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920355 | ||||||
chr8:38920358
|
G | T | 25 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0054others(22): Show | 25 | HG00408.hp2 HG01175.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+2288G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920358 | ||||||
chr8:38920360
|
T | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | NA18977.hp2 NA18982.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2290T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920360 | ||||||
chr8:38920361
|
A | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | NA18977.hp2 NA18982.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2291A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920361 | ||||||
chr8:38920374
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.141+2304T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920374 | ||||||
chr8:38920376
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(282): Show | 286 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.141+2306A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920376 | ||||||
chr8:38920378
|
G | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(282): Show | 286 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.141+2308G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920378 | ||||||
chr8:38920405
|
T | C | 1 | a0001c0001t0003g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.141+2335T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920405 | ||||||
chr8:38920434
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0003g0108 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.141+2364A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920434 | ||||||
chr8:38920459
|
G | C | 1 | a0001c0001t0005g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.141+2389G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920459 | ||||||
chr8:38920575
|
G | GT | 14 | a0001c0001t0001g0053a0001c0001t0001g0083a0001c0001t0001g0247others(11): Show | 14 | HG00408.hp1 HG00673.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+2518dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38920575 | |||||
chr8:38920607
|
C | T | 1 | a0001c0001t0055g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.141+2537C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920607 | ||||||
chr8:38920743
|
G | A | 34 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.141+2673G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920743 | ||||||
chr8:38920847
|
C | A | 1 | a0001c0001t0003g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+2777C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920847 | ||||||
chr8:38920863
|
C | T | 45 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(42): Show | 45 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.141+2793C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38920863 | ||||||
chr8:38921021
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.141+2951G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921021 | ||||||
chr8:38921197
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.141+3127G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921197 | ||||||
chr8:38921204
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.141+3134A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921204 | ||||||
chr8:38921640
|
C | T | 5 | a0001c0001t0007g0122a0001c0001t0013g0117a0001c0001t0016g0132others(2): Show | 5 | HG02257.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+3570C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921640 | ||||||
chr8:38921700
|
C | A | 1 | a0001c0001t0003g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141+3630C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38921700 | ||||||
chr8:38922129
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(269): Show | 273 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.141+4059G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922129 | ||||||
chr8:38922168
|
T | G | 15 | a0001c0001t0001g0127a0001c0001t0002g0138a0001c0001t0003g0134others(12): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+4098T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922168 | ||||||
chr8:38922248
|
C | T | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+4178C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922248 | ||||||
chr8:38922308
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0013g0117 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.141+4238G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922308 | ||||||
chr8:38922533
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.141+4463C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922533 | ||||||
chr8:38922611
|
A | G | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(45): Show | 48 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.141+4541A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38922611 | ||||||
chr8:38923088
|
A | C | 146 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(143): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.141+5018A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923088 | ||||||
chr8:38923134
|
C | T | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+5064C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923134 | ||||||
chr8:38923394
|
A | G | 3 | a0001c0001t0016g0132a0001c0001t0037g0217a0001c0007t0016g0157 | 3 | HG02257.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.141+5324A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923394 | ||||||
chr8:38923500
|
C | T | 6 | a0001c0001t0002g0229a0001c0001t0007g0122a0001c0001t0011g0158others(3): Show | 6 | HG01884.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+5430C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923500 | ||||||
chr8:38923515
|
A | T | 5 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+5445A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923515 | ||||||
chr8:38923522
|
C | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(199): Show | 203 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.141+5452C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923522 | ||||||
chr8:38923578
|
C | T | 1 | a0001c0001t0017g0194 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.141+5508C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923578 | ||||||
chr8:38923611
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0017g0194 | 2 | HG00733.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.141+5541C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923611 | ||||||
chr8:38923702
|
ACAATTGG others(18): Show |
A | 3 | a0001c0001t0003g0293a0001c0001t0036g0305a0001c0001t0040g0266 | 3 | HG02683.hp1 HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.141+5634_141+5658d others(27): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38923702 | |||||
chr8:38923970
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.141+5900G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38923970 | ||||||
chr8:38924002
|
C | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+5932C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924002 | ||||||
chr8:38924141
|
C | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+6071C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924141 | ||||||
chr8:38924143
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.141+6073C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924143 | ||||||
chr8:38924151
|
G | A | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+6081G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924151 | ||||||
chr8:38924178
|
T | C | 57 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(54): Show | 57 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.141+6108T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924178 | ||||||
chr8:38924190
|
C | T | 2 | a0001c0001t0011g0158a0001c0001t0012g0195 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.141+6120C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924190 | ||||||
chr8:38924332
|
G | A | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+6262G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924332 | ||||||
chr8:38924369
|
C | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+6299C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924369 | ||||||
chr8:38924393
|
T | C | 1 | a0002c0002t0031g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141+6323T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924393 | ||||||
chr8:38924406
|
C | T | 84 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.141+6336C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924406 | ||||||
chr8:38924497
|
G | C | 8 | a0001c0001t0001g0247a0001c0001t0001g0262a0001c0001t0001g0354others(5): Show | 8 | HG00408.hp1 NA18952.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+6427G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924497 | ||||||
chr8:38924573
|
G | A | 58 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(55): Show | 58 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.141+6503G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924573 | ||||||
chr8:38924757
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0100others(53): Show | 57 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.141+6687C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924757 | ||||||
chr8:38924800
|
G | A | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(3): Show | 6 | HG01106.hp2 HG01358.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+6730G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38924800 | ||||||
chr8:38925109
|
T | C | 80 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.141+7039T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925109 | ||||||
chr8:38925265
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.141+7195C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925265 | ||||||
chr8:38925295
|
C | T | 1 | a0001c0001t0044g0290 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.141+7225C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925295 | ||||||
chr8:38925296
|
G | A | 1 | a0001c0001t0013g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.141+7226G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925296 | ||||||
chr8:38925502
|
C | T | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.141+7432C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925502 | ||||||
chr8:38925550
|
G | A | 1 | a0001c0001t0013g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.141+7480G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925550 | ||||||
chr8:38925911
|
C | A | 1 | a0001c0001t0052g0270 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.141+7841C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925911 | ||||||
chr8:38925935
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.141+7865A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38925935 | ||||||
chr8:38926066
|
G | A | 57 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(54): Show | 57 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.141+7996G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926066 | ||||||
chr8:38926081
|
T | A | 2 | a0001c0001t0001g0364a0001c0001t0048g0317 | 2 | NA18985.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.141+8011T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926081 | ||||||
chr8:38926230
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.141+8160A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926230 | ||||||
chr8:38926381
|
C | CT | 55 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(52): Show | 55 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.141+8328dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38926381 | |||||
chr8:38926381
|
CT | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(53): Show | 56 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.141+8328delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38926381 | |||||
chr8:38926418
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.141+8348C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926418 | ||||||
chr8:38926615
|
G | A | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.141+8545G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926615 | ||||||
chr8:38926659
|
G | T | 1 | a0001c0001t0003g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.141+8589G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926659 | ||||||
chr8:38926782
|
T | G | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+8712T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926782 | ||||||
chr8:38926899
|
G | C | 22 | a0001c0001t0001g0127a0001c0001t0001g0197a0001c0001t0001g0199others(19): Show | 22 | HG00733.hp1 HG02055.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.141+8829G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926899 | ||||||
chr8:38926932
|
C | A | 4 | a0001c0001t0001g0100a0001c0001t0028g0154a0001c0001t0028g0155others(1): Show | 4 | HG01891.hp2 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+8862C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38926932 | ||||||
chr8:38927006
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.141+8936G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927006 | ||||||
chr8:38927027
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.141+8957G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927027 | ||||||
chr8:38927162
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0100others(53): Show | 57 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.142-8832A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927162 | ||||||
chr8:38927606
|
T | C | 1 | a0001c0001t0003g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.142-8388T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927606 | ||||||
chr8:38927678
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0100others(54): Show | 58 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.142-8316A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927678 | ||||||
chr8:38927893
|
G | A | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-8101G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927893 | ||||||
chr8:38927976
|
A | C | 1 | a0001c0007t0016g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142-8018A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38927976 | ||||||
chr8:38928085
|
A | G | 1 | a0001c0001t0007g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.142-7909A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928085 | ||||||
chr8:38928172
|
GCAGT | G | 16 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0138others(13): Show | 16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-7818_142-7815d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928172 | |||||
chr8:38928236
|
C | CT | 136 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.142-7738dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928236 | |||||
chr8:38928236
|
C | CTT | 56 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(53): Show | 56 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.142-7739_142-7738d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928236 | |||||
chr8:38928236
|
CT | C | 9 | a0001c0001t0001g0197a0001c0001t0001g0218a0001c0001t0001g0346others(6): Show | 9 | HG00733.hp1 HG02055.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-7738delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38928236 | |||||
chr8:38928397
|
C | T | 1 | a0001c0001t0002g0367 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.142-7597C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928397 | ||||||
chr8:38928406
|
A | T | 82 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.142-7588A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928406 | ||||||
chr8:38928474
|
C | T | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-7520C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928474 | ||||||
chr8:38928538
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-7456C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928538 | ||||||
chr8:38928549
|
C | T | 137 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0049others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.142-7445C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928549 | ||||||
chr8:38928680
|
A | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0115 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.142-7314A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928680 | ||||||
chr8:38928862
|
G | A | 2 | a0001c0001t0014g0179a0001c0001t0019g0143 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-7132G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928862 | ||||||
chr8:38928909
|
G | A | 1 | a0001c0001t0012g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.142-7085G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928909 | ||||||
chr8:38928913
|
C | G | 2 | a0001c0001t0011g0158a0001c0001t0012g0195 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.142-7081C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928913 | ||||||
chr8:38928919
|
G | A | 12 | a0001c0001t0001g0177a0001c0001t0001g0202a0001c0001t0001g0203others(9): Show | 12 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-7075G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928919 | ||||||
chr8:38928968
|
G | A | 25 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(22): Show | 25 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.142-7026G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38928968 | ||||||
chr8:38929016
|
C | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0341others(1): Show | 4 | HG00423.hp2 NA18961.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-6978C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929016 | ||||||
chr8:38929209
|
G | A | 2 | a0001c0001t0002g0318a0001c0001t0002g0348 | 2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.142-6785G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929209 | ||||||
chr8:38929248
|
A | T | 8 | a0001c0001t0001g0311a0001c0001t0001g0343a0001c0001t0002g0342others(5): Show | 8 | HG01099.hp2 HG01257.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-6746A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929248 | ||||||
chr8:38929299
|
C | A | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-6695C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929299 | ||||||
chr8:38929881
|
AT | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0218others(49): Show | 53 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-6112delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929881 | ||||||
chr8:38929952
|
C | T | 14 | a0001c0001t0001g0254a0001c0001t0001g0276a0001c0001t0001g0313others(11): Show | 14 | HG01168.hp2 HG01934.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-6042C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929952 | ||||||
chr8:38929954
|
C | T | 1 | a0001c0001t0005g0301 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.142-6040C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929954 | ||||||
chr8:38929995
|
G | A | 2 | a0001c0001t0005g0063a0001c0001t0043g0035 | 2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.142-5999G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38929995 | ||||||
chr8:38930090
|
C | G | 82 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.142-5904C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930090 | ||||||
chr8:38930160
|
G | A | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-5834G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930160 | ||||||
chr8:38930161
|
G | C | 2 | a0001c0001t0020g0012a0002c0002t0004g0123 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.142-5833G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930161 | ||||||
chr8:38930186
|
C | CTTTA | 10 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(7): Show | 10 | HG01106.hp2 HG01358.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-5780_142-5777d others(6): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | |||||
chr8:38930186
|
C | CTTTATTT others(1): Show |
53 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(50): Show | 53 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.142-5784_142-5777d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | |||||
chr8:38930186
|
C | CTTTATTT others(5): Show |
3 | a0001c0001t0001g0068a0001c0001t0002g0024a0001c0001t0002g0228 | 3 | HG02080.hp2 HG03017.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.142-5788_142-5777d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | |||||
chr8:38930186
|
C | CTTTATTT others(9): Show |
1 | a0001c0001t0001g0054 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.142-5792_142-5777d others(18): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | |||||
chr8:38930186
|
CTTTATTT others(1): Show |
C | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-5784_142-5777d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930186 | |||||
chr8:38930245
|
G | A | 1 | a0001c0001t0042g0242 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.142-5749G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930245 | ||||||
chr8:38930346
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0002g0243a0001c0001t0042g0242 | 3 | HG00639.hp2 HG01069.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.142-5648C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930346 | ||||||
chr8:38930445
|
C | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(114): Show | 118 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.142-5549C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930445 | ||||||
chr8:38930447
|
C | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(114): Show | 118 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.142-5547C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930447 | ||||||
chr8:38930496
|
G | A | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-5498G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930496 | ||||||
chr8:38930510
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.142-5484C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930510 | ||||||
chr8:38930637
|
G | A | 6 | a0001c0001t0001g0311a0001c0001t0002g0342a0001c0001t0006g0339others(3): Show | 6 | HG01099.hp2 HG01257.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-5357G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930637 | ||||||
chr8:38930646
|
CGGCAT | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(169): Show | 173 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.142-5333_142-5329d others(7): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38930646 | |||||
chr8:38930914
|
A | G | 3 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250 | 3 | HG02922.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.142-5080A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38930914 | ||||||
chr8:38931064
|
T | G | 4 | a0001c0001t0001g0314a0001c0001t0002g0318a0001c0001t0002g0348others(1): Show | 4 | HG01361.hp2 HG01496.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-4930T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931064 | ||||||
chr8:38931135
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-4859G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931135 | ||||||
chr8:38931304
|
C | T | 1 | a0001c0001t0011g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142-4690C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931304 | ||||||
chr8:38931310
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.142-4684G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931310 | ||||||
chr8:38931356
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.142-4638C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931356 | ||||||
chr8:38931593
|
G | C | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-4401G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931593 | ||||||
chr8:38931809
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-4185C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931809 | ||||||
chr8:38931980
|
A | T | 2 | a0001c0001t0002g0365a0001c0001t0002g0366 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.142-4014A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931980 | ||||||
chr8:38931995
|
C | A | 1 | a0001c0001t0049g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.142-3999C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38931995 | ||||||
chr8:38932021
|
C | T | 3 | a0001c0001t0002g0304a0001c0001t0003g0310a0001c0001t0004g0303 | 3 | NA18970.hp1 NA18980.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.142-3973C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932021 | ||||||
chr8:38932055
|
A | C | 2 | a0001c0001t0014g0179a0001c0001t0019g0143 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-3939A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932055 | ||||||
chr8:38932145
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(285): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.142-3849T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932145 | ||||||
chr8:38932173
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0011g0158others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-3821T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932173 | ||||||
chr8:38932279
|
C | T | 84 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.142-3715C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932279 | ||||||
chr8:38932497
|
G | A | 1 | a0001c0001t0016g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142-3497G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932497 | ||||||
chr8:38932675
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.142-3319G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932675 | ||||||
chr8:38932969
|
C | G | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-3025C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38932969 | ||||||
chr8:38933080
|
G | A | 16 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0138others(13): Show | 16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-2914G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933080 | ||||||
chr8:38933089
|
T | C | 16 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0138others(13): Show | 16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-2905T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933089 | ||||||
chr8:38933117
|
C | T | 20 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0138others(17): Show | 20 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-2877C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933117 | ||||||
chr8:38933218
|
A | G | 2 | a0001c0001t0016g0132a0001c0007t0016g0157 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142-2776A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933218 | ||||||
chr8:38933248
|
C | T | 16 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0138others(13): Show | 16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-2746C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933248 | ||||||
chr8:38933268
|
T | G | 196 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(193): Show | 196 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.142-2726T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933268 | ||||||
chr8:38933432
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(280): Show | 284 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.142-2562G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933432 | ||||||
chr8:38933586
|
C | CCG | 3 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0002g0140 | 3 | HG02109.hp1 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.142-2408_142-2407i others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933586 | ||||||
chr8:38933778
|
T | TAAAAAAA others(3): Show |
6 | a0001c0001t0001g0100a0001c0001t0001g0368a0001c0001t0003g0026others(3): Show | 6 | HG00733.hp1 HG01891.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2209_142-2200d others(12): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | |||||
chr8:38933778
|
T | TAAAAAAA others(4): Show |
48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(45): Show | 48 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.142-2210_142-2200d others(13): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | |||||
chr8:38933778
|
T | TAAAAAAA others(5): Show |
6 | a0001c0001t0001g0241a0001c0001t0002g0027a0001c0001t0002g0067others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2211_142-2200d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | |||||
chr8:38933778
|
T | TAAAAAAA others(6): Show |
5 | a0001c0001t0001g0054a0001c0001t0001g0068a0001c0001t0002g0024others(2): Show | 5 | HG01243.hp2 HG02080.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-2212_142-2200d others(15): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | |||||
chr8:38933778
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0003g0171 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.142-2213_142-2200d others(16): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933778 | |||||
chr8:38933790
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0037g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.142-2200_142-2199i others(44): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0275a0001c0001t0016g0149 | 2 | HG01070.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(31): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0263a0001c0001t0002g0170a0001c0001t0002g0318 | 3 | HG01175.hp2 HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(30): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(20): Show |
12 | a0001c0001t0001g0177a0001c0001t0001g0264a0001c0001t0002g0041others(9): Show | 12 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(29): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(19): Show |
16 | a0001c0001t0001g0049a0001c0001t0001g0084a0001c0001t0001g0202others(13): Show | 16 | HG00642.hp2 HG00733.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(28): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(18): Show |
23 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0098others(20): Show | 23 | HG00280.hp2 HG01106.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(27): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(17): Show |
14 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0190others(11): Show | 14 | HG01516.hp1 HG01517.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(26): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(16): Show |
5 | a0001c0001t0003g0097a0001c0001t0003g0297a0001c0001t0003g0299others(2): Show | 5 | HG01081.hp2 HG01099.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(25): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(13): Show |
4 | a0001c0001t0001g0204a0001c0001t0003g0175a0001c0001t0056g0224others(1): Show | 4 | HG00735.hp1 HG02572.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(22): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(12): Show |
22 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(19): Show | 22 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.142-2200_142-2199i others(21): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-2200_142-2199i others(20): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0013g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142-2200_142-2199i others(19): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0014g0179a0001c0001t0019g0143 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0008g0196a0001c0001t0009g0071 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.142-2200_142-2199i others(13): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933790
|
A | AAAAGAAA others(1): Show |
14 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0138others(11): Show | 14 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.142-2201_142-2200i others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38933790 | |||||
chr8:38933830
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0015g0216 | 2 | HG02027.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.142-2164A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933830 | ||||||
chr8:38933911
|
A | T | 1 | a0001c0001t0002g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-2083A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933911 | ||||||
chr8:38933985
|
C | G | 4 | a0001c0001t0001g0294a0001c0001t0001g0296a0001c0001t0002g0059others(1): Show | 4 | HG02015.hp2 HG02083.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-2009C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38933985 | ||||||
chr8:38934157
|
A | AAT | 7 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0002g0140others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-1823_142-1822d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38934157 | |||||
chr8:38934191
|
C | T | 108 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(105): Show | 108 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.142-1803C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934191 | ||||||
chr8:38934197
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.142-1797A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934197 | ||||||
chr8:38934234
|
A | G | 43 | a0001c0001t0001g0084a0001c0001t0001g0177a0001c0001t0001g0185others(40): Show | 43 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-1760A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934234 | ||||||
chr8:38934285
|
C | T | 20 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0138others(17): Show | 20 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-1709C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934285 | ||||||
chr8:38934374
|
C | T | 3 | a0001c0001t0002g0112a0001c0001t0002g0115a0001c0001t0003g0107 | 3 | HG01361.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.142-1620C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934374 | ||||||
chr8:38934410
|
C | T | 23 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.142-1584C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934410 | ||||||
chr8:38934515
|
C | G | 1 | a0001c0001t0002g0212 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.142-1479C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934515 | ||||||
chr8:38934518
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.142-1476G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934518 | ||||||
chr8:38934597
|
G | A | 1 | a0001c0001t0003g0277 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.142-1397G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934597 | ||||||
chr8:38934614
|
C | T | 1 | a0001c0001t0011g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142-1380C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934614 | ||||||
chr8:38934622
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-1372G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934622 | ||||||
chr8:38934644
|
C | A | 77 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(74): Show | 77 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.142-1350C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934644 | ||||||
chr8:38934694
|
T | G | 1 | a0001c0001t0013g0117 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142-1300T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934694 | ||||||
chr8:38934816
|
GTA | G | 110 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(107): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.142-1164_142-1163d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38934816 | |||||
chr8:38934848
|
C | T | 77 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(74): Show | 77 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.142-1146C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934848 | ||||||
chr8:38934872
|
TA | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.142-1112delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38934872 | |||||
chr8:38934873
|
A | T | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142-1121A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38934873 | ||||||
chr8:38935040
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.142-954G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935040 | ||||||
chr8:38935256
|
G | A | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-738G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935256 | ||||||
chr8:38935353
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0218others(49): Show | 53 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-641G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935353 | ||||||
chr8:38935368
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0002g0140 | 3 | HG02109.hp1 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.142-626A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935368 | ||||||
chr8:38935381
|
A | C | 1 | a0002c0002t0031g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142-613A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935381 | ||||||
chr8:38935430
|
C | CT | 16 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0007others(13): Show | 16 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-548dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 38935430 | |||||
chr8:38935457
|
G | T | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(56): Show | 59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.142-537G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935457 | ||||||
chr8:38935606
|
A | T | 9 | a0001c0001t0001g0100a0001c0001t0001g0197a0001c0001t0003g0171others(6): Show | 9 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-388A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935606 | ||||||
chr8:38935637
|
T | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(281): Show | 285 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.142-357T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935637 | ||||||
chr8:38935816
|
A | G | 1 | a0001c0001t0025g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.142-178A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 2/11 | chr8 | 38935816 | ||||||
chr8:38936115
|
G | A | 1 | a0001c0001t0013g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198+65G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936115 | ||||||
chr8:38936150
|
A | C | 1 | a0001c0001t0049g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+100A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936150 | ||||||
chr8:38936164
|
T | G | 50 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.198+114T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936164 | ||||||
chr8:38936181
|
C | A | 1 | a0001c0001t0003g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.198+131C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936181 | ||||||
chr8:38936312
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0069 | 2 | HG02523.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.198+262C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936312 | ||||||
chr8:38936318
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0218others(52): Show | 56 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.198+268A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936318 | ||||||
chr8:38936320
|
G | A | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+270G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936320 | ||||||
chr8:38936357
|
A | G | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+307A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936357 | ||||||
chr8:38936408
|
T | C | 1 | a0001c0001t0005g0361 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.198+358T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936408 | ||||||
chr8:38936558
|
C | T | 1 | a0001c0001t0008g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.198+508C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936558 | ||||||
chr8:38936580
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198+530A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936580 | ||||||
chr8:38936858
|
G | C | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+808G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936858 | ||||||
chr8:38936939
|
A | G | 112 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(109): Show | 112 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.198+889A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936939 | ||||||
chr8:38936946
|
T | C | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+896T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38936946 | ||||||
chr8:38937128
|
A | T | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1078A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937128 | ||||||
chr8:38937268
|
C | T | 1 | a0001c0001t0049g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+1218C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937268 | ||||||
chr8:38937313
|
C | G | 1 | a0001c0001t0009g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198+1263C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937313 | ||||||
chr8:38937431
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0002g0033others(2): Show | 5 | HG02015.hp1 HG02155.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+1381G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937431 | ||||||
chr8:38937481
|
G | A | 3 | a0001c0001t0013g0117a0001c0001t0013g0152a0001c0001t0027g0153 | 3 | HG02647.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.198+1431G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937481 | ||||||
chr8:38937485
|
G | C | 76 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(73): Show | 76 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.198+1435G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937485 | ||||||
chr8:38937521
|
G | A | 1 | a0001c0001t0001g0336 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.198+1471G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937521 | ||||||
chr8:38937684
|
A | T | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1634A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937684 | ||||||
chr8:38937709
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.198+1659C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937709 | ||||||
chr8:38937844
|
C | T | 4 | a0001c0001t0002g0180a0001c0001t0013g0146a0001c0001t0045g0302others(1): Show | 4 | HG02559.hp2 HG02818.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1794C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937844 | ||||||
chr8:38937870
|
C | T | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198+1820C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937870 | ||||||
chr8:38937871
|
G | A | 1 | a0001c0001t0006g0373 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.198+1821G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937871 | ||||||
chr8:38937898
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0006g0072 | 2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.198+1848C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937898 | ||||||
chr8:38937900
|
T | G | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1850T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937900 | ||||||
chr8:38937901
|
G | C | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1851G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937901 | ||||||
chr8:38937909
|
G | T | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1859G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937909 | ||||||
chr8:38937950
|
A | T | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1900A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937950 | ||||||
chr8:38937951
|
G | C | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1901G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937951 | ||||||
chr8:38937952
|
T | TGTGTTCT others(10): Show |
1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1903_198+1904i others(19): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38937952 | |||||
chr8:38937956
|
G | T | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1906G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937956 | ||||||
chr8:38937971
|
G | C | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1921G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937971 | ||||||
chr8:38937973
|
C | A | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1923C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937973 | ||||||
chr8:38937973
|
C | T | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+1923C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38937973 | ||||||
chr8:38938091
|
T | G | 22 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0003g0134others(19): Show | 22 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.198+2041T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938091 | ||||||
chr8:38938129
|
C | A | 31 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(28): Show | 31 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.198+2079C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938129 | ||||||
chr8:38938129
|
C | T | 9 | a0001c0001t0001g0100a0001c0001t0001g0197a0001c0001t0003g0171others(6): Show | 9 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+2079C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938129 | ||||||
chr8:38938177
|
G | A | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2127G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938177 | ||||||
chr8:38938383
|
A | T | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2333A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938383 | ||||||
chr8:38938452
|
G | GCTGCCAC others(5): Show |
8 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0325others(5): Show | 8 | HG00621.hp1 HG00621.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+2409_198+2420d others(14): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938452 | |||||
chr8:38938667
|
A | C | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2617A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938667 | ||||||
chr8:38938671
|
C | A | 1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2621C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938671 | ||||||
chr8:38938758
|
G | GTGGATGG others(84): Show |
1 | a0001c0001t0002g0362 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+2731_198+2732i others(93): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938758 | |||||
chr8:38938857
|
C | T | 2 | a0001c0001t0002g0193a0001c0001t0005g0192 | 2 | NA19009.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.198+2807C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38938857 | ||||||
chr8:38938900
|
C | CT | 107 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0021others(104): Show | 108 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.198+2865dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938900 | |||||
chr8:38938900
|
CT | C | 9 | a0001c0001t0001g0083a0001c0001t0001g0251a0001c0001t0003g0171others(6): Show | 9 | HG01168.hp2 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+2865delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38938900 | |||||
chr8:38939013
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(260): Show | 264 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.198+2963T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939013 | ||||||
chr8:38939368
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0218others(52): Show | 56 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.198+3318A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939368 | ||||||
chr8:38939420
|
A | T | 19 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0003g0134others(16): Show | 19 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+3370A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939420 | ||||||
chr8:38939637
|
G | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0045 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.198+3587G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939637 | ||||||
chr8:38939679
|
C | T | 15 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0003g0134others(12): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+3629C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939679 | ||||||
chr8:38939698
|
A | G | 1 | a0006c0009t0008g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.198+3648A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939698 | ||||||
chr8:38939774
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(285): Show | 289 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.198+3724T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939774 | ||||||
chr8:38939818
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(286): Show | 290 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.198+3768A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939818 | ||||||
chr8:38939996
|
G | T | 2 | a0001c0001t0003g0175a0001c0001t0013g0121 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-3793G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38939996 | ||||||
chr8:38940045
|
G | T | 1 | a0001c0001t0007g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-3744G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940045 | ||||||
chr8:38940073
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(239): Show | 243 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.199-3716C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940073 | ||||||
chr8:38940093
|
T | TA | 22 | a0001c0001t0001g0031a0001c0001t0001g0103a0001c0001t0001g0127others(19): Show | 22 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-3675dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | |||||
chr8:38940093
|
TA | T | 90 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(87): Show | 90 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.199-3675delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | |||||
chr8:38940093
|
TAA | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0043others(107): Show | 111 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.199-3676_199-3675d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | |||||
chr8:38940093
|
TAAA | T | 6 | a0001c0001t0002g0229a0001c0001t0003g0255a0001c0001t0007g0122others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-3677_199-3675d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940093 | |||||
chr8:38940124
|
G | A | 1 | a0001c0001t0003g0307 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-3665G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940124 | ||||||
chr8:38940142
|
A | G | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-3647A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940142 | ||||||
chr8:38940315
|
CT | C | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3472delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940315 | |||||
chr8:38940322
|
C | T | 96 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(93): Show | 96 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.199-3467C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940322 | ||||||
chr8:38940398
|
C | T | 1 | a0001c0001t0013g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-3391C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940398 | ||||||
chr8:38940485
|
G | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3304G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940485 | ||||||
chr8:38940486
|
G | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3303G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940486 | ||||||
chr8:38940494
|
T | G | 1 | a0001c0001t0001g0311 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.199-3295T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940494 | ||||||
chr8:38940539
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.199-3250G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940539 | ||||||
chr8:38940548
|
A | T | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-3241A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940548 | ||||||
chr8:38940630
|
C | G | 23 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-3159C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940630 | ||||||
chr8:38940631
|
G | A | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(56): Show | 59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.199-3158G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940631 | ||||||
chr8:38940650
|
C | CG | 99 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0029others(96): Show | 100 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.199-3127dupG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | |||||
chr8:38940650
|
C | CGG | 73 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0043others(70): Show | 74 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.199-3128_199-3127d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | |||||
chr8:38940650
|
C | CGGG | 19 | a0001c0001t0001g0008a0001c0001t0001g0199a0001c0001t0001g0221others(16): Show | 19 | HG00621.hp1 HG00621.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.199-3129_199-3127d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | |||||
chr8:38940650
|
CG | C | 52 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0039others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.199-3127delG | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940650 | |||||
chr8:38940656
|
G | C | 3 | a0001c0001t0003g0060a0001c0001t0005g0063a0001c0001t0043g0035 | 3 | HG00323.hp2 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.199-3133G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940656 | ||||||
chr8:38940657
|
G | GT | 4 | a0001c0001t0007g0148a0001c0001t0007g0150a0001c0001t0013g0151others(1): Show | 4 | HG01891.hp1 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3132_199-3131i others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940657 | ||||||
chr8:38940696
|
T | C | 2 | a0001c0001t0003g0175a0001c0001t0013g0121 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-3093T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38940696 | ||||||
chr8:38940893
|
A | ATT | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(56): Show | 59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.199-2895_199-2894d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940893 | |||||
chr8:38940894
|
T | TTA | 36 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(33): Show | 36 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.199-2882_199-2881d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38940894 | |||||
chr8:38941030
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.199-2759T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941030 | ||||||
chr8:38941055
|
CT | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(243): Show | 247 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.199-2716delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38941055 | |||||
chr8:38941055
|
CTT | C | 9 | a0001c0001t0001g0329a0001c0001t0003g0026a0001c0001t0003g0042others(6): Show | 9 | HG01069.hp2 HG02451.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-2717_199-2716d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38941055 | |||||
chr8:38941110
|
G | A | 2 | a0001c0001t0003g0175a0001c0001t0013g0121 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-2679G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941110 | ||||||
chr8:38941117
|
C | T | 2 | a0001c0001t0016g0132a0001c0007t0016g0157 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-2672C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941117 | ||||||
chr8:38941149
|
C | T | 1 | a0001c0001t0002g0335 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.199-2640C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941149 | ||||||
chr8:38941159
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0007g0161a0001c0001t0017g0194 | 3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.199-2630C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941159 | ||||||
chr8:38941218
|
G | C | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.199-2571G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941218 | ||||||
chr8:38941256
|
A | C | 3 | a0001c0001t0001g0197a0001c0001t0007g0161a0001c0001t0017g0194 | 3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.199-2533A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941256 | ||||||
chr8:38941301
|
C | T | 15 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0003g0134others(12): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-2488C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941301 | ||||||
chr8:38941335
|
C | T | 23 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-2454C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941335 | ||||||
chr8:38941382
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.199-2407A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941382 | ||||||
chr8:38941539
|
G | A | 77 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(74): Show | 77 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.199-2250G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941539 | ||||||
chr8:38941601
|
A | T | 1 | a0001c0001t0037g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.199-2188A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941601 | ||||||
chr8:38941687
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-2102T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941687 | ||||||
chr8:38941794
|
A | T | 23 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-1995A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38941794 | ||||||
chr8:38942124
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0019others(158): Show | 162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.199-1665G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942124 | ||||||
chr8:38942359
|
C | T | 1 | a0001c0001t0049g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.199-1430C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942359 | ||||||
chr8:38942360
|
G | T | 76 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(73): Show | 76 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.199-1429G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942360 | ||||||
chr8:38942453
|
C | CA | 5 | a0001c0001t0001g0169a0001c0001t0001g0316a0001c0001t0002g0069others(2): Show | 5 | HG01515.hp1 HG02523.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-1329dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 38942453 | |||||
chr8:38942454
|
A | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-1335A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942454 | ||||||
chr8:38942466
|
C | T | 7 | a0001c0001t0001g0073a0001c0001t0001g0280a0001c0001t0002g0074others(4): Show | 7 | HG01257.hp1 HG01258.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-1323C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942466 | ||||||
chr8:38942546
|
G | C | 2 | a0001c0001t0003g0175a0001c0001t0013g0121 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-1243G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942546 | ||||||
chr8:38942610
|
C | A | 5 | a0001c0001t0002g0229a0001c0001t0007g0122a0001c0001t0011g0158others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-1179C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942610 | ||||||
chr8:38942777
|
G | A | 3 | a0001c0001t0014g0179a0001c0001t0019g0143a0001c0001t0037g0217 | 3 | HG02451.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199-1012G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942777 | ||||||
chr8:38942842
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.199-947G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942842 | ||||||
chr8:38942899
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.199-890C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942899 | ||||||
chr8:38942947
|
G | A | 1 | a0001c0001t0011g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199-842G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38942947 | ||||||
chr8:38943083
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0218others(48): Show | 52 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.199-706C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943083 | ||||||
chr8:38943153
|
A | G | 2 | a0001c0001t0003g0175a0001c0001t0013g0121 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.199-636A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943153 | ||||||
chr8:38943246
|
T | A | 1 | a0001c0001t0002g0347 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.199-543T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943246 | ||||||
chr8:38943281
|
G | T | 24 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0002g0229others(21): Show | 24 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-508G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943281 | ||||||
chr8:38943425
|
G | A | 76 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(73): Show | 76 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.199-364G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943425 | ||||||
chr8:38943446
|
A | G | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.199-343A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943446 | ||||||
chr8:38943542
|
A | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-247A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943542 | ||||||
chr8:38943561
|
C | T | 3 | a0001c0001t0001g0313a0001c0001t0001g0337a0001c0001t0010g0279 | 3 | NA18612.hp2 NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.199-228C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943561 | ||||||
chr8:38943767
|
T | C | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-22T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 3/11 | chr8 | 38943767 | ||||||
chr8:38944024
|
A | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0218others(48): Show | 52 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.247+187A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944024 | ||||||
chr8:38944041
|
G | A | 2 | a0001c0001t0012g0184a0001c0001t0035g0183 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.247+204G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944041 | ||||||
chr8:38944107
|
A | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.247+270A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944107 | ||||||
chr8:38944121
|
A | G | 105 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(102): Show | 105 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.247+284A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944121 | ||||||
chr8:38944163
|
A | G | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.247+326A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944163 | ||||||
chr8:38944168
|
A | C | 3 | a0001c0001t0002g0229a0001c0001t0007g0122a0002c0002t0051g0131 | 3 | HG02895.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.247+331A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944168 | ||||||
chr8:38944221
|
G | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(107): Show | 111 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.247+384G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944221 | ||||||
chr8:38944236
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0002g0140others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+399C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944236 | ||||||
chr8:38944237
|
G | A | 2 | a0001c0001t0016g0132a0001c0007t0016g0157 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.247+400G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944237 | ||||||
chr8:38944369
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.247+532T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944369 | ||||||
chr8:38944409
|
C | T | 1 | a0001c0001t0012g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.247+572C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944409 | ||||||
chr8:38944504
|
G | GA | 111 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(108): Show | 111 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.247+677dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 38944504 | |||||
chr8:38944693
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0045g0302 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.247+856A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944693 | ||||||
chr8:38944738
|
C | T | 30 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.247+901C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944738 | ||||||
chr8:38944777
|
T | C | 2 | a0001c0001t0011g0158a0001c0001t0012g0195 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.247+940T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944777 | ||||||
chr8:38944931
|
ATGT | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.247+1098_247+1100d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr8 | 38944931 | |||||
chr8:38944964
|
G | C | 2 | a0001c0001t0016g0132a0001c0007t0016g0157 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.247+1127G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944964 | ||||||
chr8:38944968
|
C | T | 1 | a0001c0001t0008g0288 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.247+1131C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944968 | ||||||
chr8:38944973
|
A | G | 1 | a0001c0001t0035g0183 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.247+1136A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38944973 | ||||||
chr8:38945052
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0007g0161a0001c0001t0017g0194 | 3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.248-1072G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945052 | ||||||
chr8:38945069
|
C | T | 2 | a0001c0001t0028g0154a0001c0001t0028g0155 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.248-1055C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945069 | ||||||
chr8:38945147
|
G | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-977G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945147 | ||||||
chr8:38945167
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0007g0161a0001c0001t0017g0194 | 3 | HG00733.hp1 HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.248-957G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945167 | ||||||
chr8:38945180
|
C | G | 3 | a0001c0001t0013g0117a0001c0001t0013g0152a0001c0001t0027g0153 | 3 | HG02647.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.248-944C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945180 | ||||||
chr8:38945208
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0218others(50): Show | 54 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.248-916T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945208 | ||||||
chr8:38945369
|
A | T | 2 | a0001c0001t0014g0179a0001c0001t0019g0143 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.248-755A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945369 | ||||||
chr8:38945374
|
C | G | 2 | a0001c0001t0014g0179a0001c0001t0019g0143 | 2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.248-750C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945374 | ||||||
chr8:38945437
|
G | A | 15 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0003g0134others(12): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.248-687G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945437 | ||||||
chr8:38945441
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0006g0072 | 2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.248-683C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945441 | ||||||
chr8:38945639
|
G | A | 4 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0275others(1): Show | 4 | HG00642.hp1 HG01070.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-485G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945639 | ||||||
chr8:38945672
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.248-452A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945672 | ||||||
chr8:38945814
|
G | T | 2 | a0001c0001t0001g0100a0001c0001t0032g0101 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.248-310G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945814 | ||||||
chr8:38945850
|
G | A | 1 | a0001c0001t0007g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.248-274G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945850 | ||||||
chr8:38945883
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.248-241G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945883 | ||||||
chr8:38945894
|
T | C | 1 | a0001c0001t0013g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.248-230T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38945894 | ||||||
chr8:38946033
|
T | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(29): Show | 32 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.248-91T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 4/11 | chr8 | 38946033 | ||||||
chr8:38946362
|
G | A | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.345+141G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946362 | ||||||
chr8:38946375
|
G | T | 76 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(73): Show | 76 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.345+154G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946375 | ||||||
chr8:38946487
|
G | A | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.345+266G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946487 | ||||||
chr8:38946551
|
A | G | 112 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0049others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.345+330A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946551 | ||||||
chr8:38946708
|
C | A | 258 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(255): Show | 258 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.345+487C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946708 | ||||||
chr8:38946779
|
T | C | 1 | a0001c0001t0009g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.345+558T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38946779 | ||||||
chr8:38947069
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.345+848T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947069 | ||||||
chr8:38947111
|
C | G | 281 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(278): Show | 281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.345+890C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947111 | ||||||
chr8:38947160
|
AAG | A | 163 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(160): Show | 163 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.345+946_345+947del others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38947160 | |||||
chr8:38947239
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.345+1018C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947239 | ||||||
chr8:38947398
|
C | T | 4 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0011g0164others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+1177C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947398 | ||||||
chr8:38947404
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0006g0072 | 2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.345+1183C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947404 | ||||||
chr8:38947428
|
C | T | 4 | a0001c0001t0014g0248a0001c0001t0014g0249a0001c0001t0014g0250others(1): Show | 4 | HG02896.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+1207C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947428 | ||||||
chr8:38947443
|
T | G | 1 | a0001c0001t0002g0212 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.345+1222T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947443 | ||||||
chr8:38947531
|
G | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.345+1310G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947531 | ||||||
chr8:38947552
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.345+1331G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947552 | ||||||
chr8:38947560
|
C | G | 2 | a0001c0001t0016g0132a0001c0007t0016g0157 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.345+1339C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947560 | ||||||
chr8:38947577
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345+1356C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947577 | ||||||
chr8:38947596
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.345+1375C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947596 | ||||||
chr8:38947614
|
G | A | 2 | a0001c0001t0003g0175a0001c0001t0013g0121 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.345+1393G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947614 | ||||||
chr8:38947881
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.345+1660G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947881 | ||||||
chr8:38947918
|
C | T | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(56): Show | 59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+1697C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947918 | ||||||
chr8:38947963
|
G | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0031others(27): Show | 30 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.345+1742G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38947963 | ||||||
chr8:38948010
|
C | G | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(56): Show | 59 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+1789C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948010 | ||||||
chr8:38948025
|
G | A | 3 | a0001c0001t0002g0229a0001c0001t0007g0122a0002c0002t0051g0131 | 3 | HG02895.hp1 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.345+1804G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948025 | ||||||
chr8:38948085
|
C | CA | 82 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0043others(79): Show | 83 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.345+1883dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948085 | |||||
chr8:38948085
|
C | CAAA | 74 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(71): Show | 74 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.345+1881_345+1883d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948085 | |||||
chr8:38948085
|
CA | C | 11 | a0001c0001t0001g0197a0001c0001t0001g0363a0001c0001t0002g0304others(8): Show | 11 | HG00733.hp1 HG02630.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.345+1883delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948085 | |||||
chr8:38948118
|
CCTT | C | 5 | a0001c0001t0001g0100a0001c0001t0001g0197a0001c0001t0007g0161others(2): Show | 5 | HG00733.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+1901_345+1903d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38948118 | |||||
chr8:38948315
|
C | T | 78 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(75): Show | 78 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.345+2094C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948315 | ||||||
chr8:38948341
|
T | A | 49 | a0001c0001t0001g0043a0001c0001t0001g0218a0001c0001t0001g0220others(46): Show | 49 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.345+2120T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948341 | ||||||
chr8:38948380
|
A | T | 2 | a0001c0001t0003g0175a0001c0001t0013g0121 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.345+2159A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948380 | ||||||
chr8:38948507
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.345+2286A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948507 | ||||||
chr8:38948550
|
G | A | 166 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(163): Show | 166 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.346-2300G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948550 | ||||||
chr8:38948592
|
G | T | 15 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0003g0134others(12): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.346-2258G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948592 | ||||||
chr8:38948638
|
T | C | 2 | a0001c0001t0007g0163a0001c0001t0053g0005 | 2 | HG01255.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.346-2212T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948638 | ||||||
chr8:38948787
|
G | A | 15 | a0001c0001t0001g0127a0001c0001t0001g0199a0001c0001t0003g0134others(12): Show | 15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.346-2063G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948787 | ||||||
chr8:38948868
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0002g0140others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-1982T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948868 | ||||||
chr8:38948901
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346-1949C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948901 | ||||||
chr8:38948937
|
C | T | 1 | a0001c0001t0011g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.346-1913C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948937 | ||||||
chr8:38948946
|
C | A | 56 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0081others(53): Show | 56 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.346-1904C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948946 | ||||||
chr8:38948985
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.346-1865C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38948985 | ||||||
chr8:38949006
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.346-1844G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949006 | ||||||
chr8:38949051
|
A | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0197a0001c0001t0007g0161others(1): Show | 4 | HG00733.hp1 HG02148.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-1799A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949051 | ||||||
chr8:38949114
|
G | A | 238 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(235): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.346-1736G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949114 | ||||||
chr8:38949189
|
C | T | 1 | a0001c0001t0002g0347 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.346-1661C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949189 | ||||||
chr8:38949235
|
T | C | 1 | a0001c0001t0001g0308 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.346-1615T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949235 | ||||||
chr8:38949350
|
A | T | 11 | a0001c0001t0002g0014a0001c0001t0007g0163a0001c0001t0009g0133others(8): Show | 11 | HG02257.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.346-1500A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949350 | ||||||
chr8:38949416
|
T | C | 16 | a0001c0001t0002g0007a0001c0001t0002g0201a0001c0001t0003g0175others(13): Show | 16 | HG01192.hp1 HG01884.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.346-1434T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949416 | ||||||
chr8:38949636
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.346-1214A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949636 | ||||||
chr8:38949696
|
C | T | 40 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0037others(37): Show | 40 | HG00323.hp2 HG00621.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.346-1154C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949696 | ||||||
chr8:38949766
|
A | G | 152 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0029others(149): Show | 152 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.346-1084A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949766 | ||||||
chr8:38949910
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.346-940C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38949910 | ||||||
chr8:38950019
|
T | G | 3 | a0001c0001t0009g0071a0001c0001t0020g0012a0001c0001t0032g0101 | 3 | HG02055.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346-831T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950019 | ||||||
chr8:38950055
|
A | AT | 14 | a0001c0001t0001g0100a0001c0001t0002g0014a0001c0001t0003g0175others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.346-788dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38950055 | |||||
chr8:38950360
|
G | A | 2 | a0001c0001t0002g0109a0001c0001t0018g0095 | 2 | NA18982.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.346-490G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950360 | ||||||
chr8:38950505
|
G | GT | 119 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0021others(116): Show | 119 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.346-336dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 38950505 | |||||
chr8:38950529
|
T | G | 1 | a0001c0001t0002g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346-321T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950529 | ||||||
chr8:38950530
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346-320A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950530 | ||||||
chr8:38950532
|
C | A | 1 | a0001c0001t0002g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346-318C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950532 | ||||||
chr8:38950561
|
C | T | 45 | a0001c0001t0001g0202a0001c0001t0001g0214a0001c0001t0001g0264others(42): Show | 46 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.346-289C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950561 | ||||||
chr8:38950699
|
G | C | 53 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0031others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.346-151G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950699 | ||||||
chr8:38950730
|
C | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0055others(7): Show | 10 | HG02132.hp1 HG02155.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.346-120C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950730 | ||||||
chr8:38950735
|
G | C | 1 | a0001c0001t0012g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.346-115G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950735 | ||||||
chr8:38950811
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.346-39G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 5/11 | chr8 | 38950811 | ||||||
chr8:38951041
|
A | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0100a0001c0001t0002g0180others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+51A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951041 | ||||||
chr8:38951072
|
T | C | 41 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(38): Show | 41 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.486+82T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951072 | ||||||
chr8:38951094
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(284): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.486+104A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951094 | ||||||
chr8:38951109
|
G | C | 1 | a0001c0001t0003g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.486+119G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951109 | ||||||
chr8:38951139
|
T | G | 349 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(346): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.486+149T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951139 | ||||||
chr8:38951229
|
G | T | 1 | a0001c0001t0002g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.486+239G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951229 | ||||||
chr8:38951234
|
G | A | 151 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.486+244G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951234 | ||||||
chr8:38951239
|
C | T | 39 | a0001c0001t0001g0191a0001c0001t0001g0271a0001c0001t0001g0276others(36): Show | 39 | HG00621.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.486+249C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951239 | ||||||
chr8:38951261
|
T | C | 1 | a0001c0001t0003g0299 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.486+271T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951261 | ||||||
chr8:38951427
|
G | A | 153 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(150): Show | 153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.486+437G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951427 | ||||||
chr8:38951469
|
G | GT | 10 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0264others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.486+503dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | |||||
chr8:38951469
|
GT | G | 26 | a0001c0001t0001g0053a0001c0001t0001g0093a0001c0001t0001g0185others(23): Show | 26 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.486+503delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | |||||
chr8:38951469
|
GTT | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0038others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.486+502_486+503del others(2): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | |||||
chr8:38951469
|
GTTT | G | 52 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(49): Show | 52 | HG00609.hp1 HG00733.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.486+501_486+503del others(3): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 38951469 | |||||
chr8:38951611
|
A | C | 1 | a0001c0001t0011g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.487-555A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951611 | ||||||
chr8:38951737
|
C | T | 1 | a0001c0001t0015g0334 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.487-429C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951737 | ||||||
chr8:38951863
|
T | C | 1 | a0001c0001t0011g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487-303T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951863 | ||||||
chr8:38951926
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.487-240T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38951926 | ||||||
chr8:38952003
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.487-163G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38952003 | ||||||
chr8:38952138
|
C | T | 1 | a0001c0001t0006g0268 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.487-28C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38952138 | ||||||
chr8:38952145
|
A | C | 340 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(337): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.487-21A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 6/11 | chr8 | 38952145 | ||||||
chr8:38952342
|
G | C | 2 | a0001c0001t0003g0104a0001c0001t0013g0146 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.633+30G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952342 | ||||||
chr8:38952344
|
T | A | 1 | a0001c0001t0009g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.633+32T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952344 | ||||||
chr8:38952534
|
G | A | 5 | a0001c0001t0012g0182a0001c0001t0012g0184a0001c0001t0027g0153others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.634-102G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952534 | ||||||
chr8:38952603
|
G | A | 2 | a0001c0001t0003g0034a0001c0001t0011g0166 | 2 | NA18965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.634-33G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 7/11 | chr8 | 38952603 | ||||||
chr8:38952720
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.702+16G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38952720 | ||||||
chr8:38952839
|
A | G | 1 | a0001c0001t0027g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.702+135A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38952839 | ||||||
chr8:38952876
|
C | T | 4 | a0002c0002t0001g0231a0002c0002t0004g0123a0002c0002t0031g0046others(1): Show | 4 | HG02723.hp2 HG02895.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+172C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38952876 | ||||||
chr8:38953189
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0049others(63): Show | 67 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.703-108A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 8/11 | chr8 | 38953189 | ||||||
chr8:38953588
|
A | G | 1 | a0001c0001t0005g0357 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.773+221A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38953588 | ||||||
chr8:38953840
|
G | A | 1 | a0001c0001t0007g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.773+473G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38953840 | ||||||
chr8:38953979
|
C | T | 42 | a0001c0001t0001g0052a0001c0001t0001g0185a0001c0001t0001g0191others(39): Show | 43 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.773+612C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38953979 | ||||||
chr8:38954044
|
G | A | 1 | a0001c0001t0003g0299 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.773+677G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954044 | ||||||
chr8:38954111
|
G | A | 1 | a0002c0002t0001g0231 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.773+744G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954111 | ||||||
chr8:38954186
|
T | A | 1 | a0001c0001t0040g0266 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.773+819T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954186 | ||||||
chr8:38954214
|
C | T | 1 | a0001c0001t0011g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.773+847C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954214 | ||||||
chr8:38954383
|
G | A | 7 | a0001c0001t0011g0164a0001c0001t0012g0182a0001c0001t0012g0184others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.773+1016G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954383 | ||||||
chr8:38954447
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.773+1080C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954447 | ||||||
chr8:38954730
|
A | T | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.773+1363A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954730 | ||||||
chr8:38954774
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.773+1407T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954774 | ||||||
chr8:38954853
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.773+1486C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954853 | ||||||
chr8:38954890
|
C | T | 1 | a0001c0007t0016g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.773+1523C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954890 | ||||||
chr8:38954958
|
C | T | 39 | a0001c0001t0001g0052a0001c0001t0001g0185a0001c0001t0001g0191others(36): Show | 40 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.773+1591C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954958 | ||||||
chr8:38954966
|
G | A | 1 | a0001c0001t0011g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.773+1599G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954966 | ||||||
chr8:38954987
|
T | C | 1 | a0001c0001t0032g0101 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.773+1620T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38954987 | ||||||
chr8:38955313
|
T | C | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.773+1946T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955313 | ||||||
chr8:38955333
|
G | A | 1 | a0001c0001t0019g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.773+1966G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955333 | ||||||
chr8:38955374
|
A | T | 1 | a0001c0001t0001g0282 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.774-1949A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955374 | ||||||
chr8:38955528
|
C | T | 332 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.774-1795C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955528 | ||||||
chr8:38955661
|
C | G | 16 | a0001c0001t0001g0015a0001c0001t0001g0100a0001c0001t0003g0134others(13): Show | 16 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.774-1662C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955661 | ||||||
chr8:38955908
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.774-1415T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955908 | ||||||
chr8:38955922
|
C | T | 1 | a0001c0001t0004g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.774-1401C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38955922 | ||||||
chr8:38956014
|
A | G | 5 | a0001c0001t0002g0041a0001c0001t0002g0365a0001c0001t0002g0366others(2): Show | 5 | HG00735.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-1309A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956014 | ||||||
chr8:38956041
|
A | C | 2 | a0002c0002t0031g0046a0002c0002t0051g0131 | 2 | HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.774-1282A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956041 | ||||||
chr8:38956081
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(177): Show | 181 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.774-1242C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956081 | ||||||
chr8:38956315
|
G | A | 1 | a0001c0001t0049g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.774-1008G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956315 | ||||||
chr8:38956327
|
G | A | 130 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(127): Show | 130 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.774-996G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956327 | ||||||
chr8:38956645
|
T | C | 348 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(345): Show | 350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.774-678T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956645 | ||||||
chr8:38956667
|
G | A | 1 | a0001c0001t0037g0217 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.774-656G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956667 | ||||||
chr8:38956696
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774-627A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956696 | ||||||
chr8:38956768
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0354a0001c0001t0007g0300 | 3 | NA18995.hp1 NA19075.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.774-555G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956768 | ||||||
chr8:38956843
|
G | A | 3 | a0001c0001t0007g0129a0001c0001t0007g0130a0001c0001t0016g0149 | 3 | HG02622.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.774-480G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956843 | ||||||
chr8:38956973
|
A | G | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.774-350A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38956973 | ||||||
chr8:38957148
|
G | A | 1 | a0001c0001t0003g0299 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.774-175G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38957148 | ||||||
chr8:38957160
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.774-163C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38957160 | ||||||
chr8:38957176
|
A | G | 1 | a0001c0001t0038g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.774-147A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 9/11 | chr8 | 38957176 | ||||||
chr8:38957632
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0004g0257 | 2 | NA19007.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.837+246G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957632 | ||||||
chr8:38957669
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.837+283G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957669 | ||||||
chr8:38957675
|
C | T | 105 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(102): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.837+289C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957675 | ||||||
chr8:38957909
|
G | A | 3 | a0001c0001t0001g0264a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG00642.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.837+523G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957909 | ||||||
chr8:38957915
|
C | T | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+529C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957915 | ||||||
chr8:38957918
|
A | G | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+532A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957918 | ||||||
chr8:38957946
|
G | A | 1 | a0001c0001t0019g0143 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.837+560G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38957946 | ||||||
chr8:38958004
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.837+618C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958004 | ||||||
chr8:38958176
|
A | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.837+790A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958176 | ||||||
chr8:38958246
|
C | T | 1 | a0001c0001t0011g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.837+860C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958246 | ||||||
chr8:38958322
|
C | CA | 216 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.837+944dupA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38958322 | |||||
chr8:38958337
|
C | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.837+951C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958337 | ||||||
chr8:38958468
|
C | T | 1 | a0001c0001t0017g0194 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.837+1082C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958468 | ||||||
chr8:38958536
|
C | G | 140 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(137): Show | 140 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.837+1150C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958536 | ||||||
chr8:38958547
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0243 | 2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.837+1161C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958547 | ||||||
chr8:38958785
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.837+1399G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958785 | ||||||
chr8:38958830
|
G | A | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+1444G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958830 | ||||||
chr8:38958873
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.837+1487T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958873 | ||||||
chr8:38958885
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.837+1499C>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958885 | ||||||
chr8:38958981
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.837+1595T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38958981 | ||||||
chr8:38959356
|
G | T | 1 | a0001c0001t0046g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.837+1970G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959356 | ||||||
chr8:38959505
|
T | A | 72 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0030others(69): Show | 73 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.837+2119T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959505 | ||||||
chr8:38959645
|
T | A | 11 | a0001c0001t0012g0139a0001c0001t0012g0182a0001c0001t0012g0184others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+2259T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959645 | ||||||
chr8:38959768
|
G | A | 1 | a0001c0001t0016g0004 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.837+2382G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959768 | ||||||
chr8:38959819
|
G | A | 1 | a0001c0001t0049g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.837+2433G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959819 | ||||||
chr8:38959894
|
A | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.837+2508A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38959894 | ||||||
chr8:38960304
|
A | G | 1 | a0001c0001t0038g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.837+2918A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960304 | ||||||
chr8:38960358
|
C | T | 1 | a0001c0001t0003g0085 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.837+2972C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960358 | ||||||
chr8:38960550
|
AC | A | 3 | a0001c0001t0003g0107a0001c0001t0003g0210a0001c0001t0022g0222 | 3 | HG00280.hp2 HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.837+3165delC | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960550 | ||||||
chr8:38960552
|
A | G | 1 | a0001c0001t0020g0012 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.837+3166A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960552 | ||||||
chr8:38960646
|
A | G | 13 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0071others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+3260A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960646 | ||||||
chr8:38960732
|
G | C | 2 | a0001c0001t0019g0124a0001c0001t0019g0143 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.837+3346G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960732 | ||||||
chr8:38960855
|
A | G | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+3469A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960855 | ||||||
chr8:38960893
|
A | G | 4 | a0001c0001t0020g0012a0001c0001t0032g0101a0002c0002t0031g0046others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+3507A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960893 | ||||||
chr8:38960905
|
G | C | 2 | a0001c0001t0022g0223a0001c0001t0039g0274 | 2 | HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.837+3519G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38960905 | ||||||
chr8:38961039
|
T | G | 13 | a0001c0001t0012g0139a0001c0001t0012g0182a0001c0001t0012g0184others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+3653T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961039 | ||||||
chr8:38961346
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0199a0001c0001t0007g0161others(1): Show | 4 | HG02630.hp1 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+3960G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961346 | ||||||
chr8:38961381
|
AC | A | 3 | a0001c0001t0004g0087a0001c0001t0004g0246a0001c0001t0004g0286 | 3 | HG00408.hp2 HG02056.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.837+3996delC | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961381 | ||||||
chr8:38961408
|
G | A | 1 | a0001c0001t0034g0181 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.837+4022G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961408 | ||||||
chr8:38961485
|
C | T | 1 | a0001c0001t0006g0268 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.837+4099C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961485 | ||||||
chr8:38961534
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0138a0001c0001t0002g0140others(3): Show | 6 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+4148C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961534 | ||||||
chr8:38961822
|
CGTTTAAC others(1): Show |
C | 106 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(103): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.837+4445_837+4452d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38961822 | |||||
chr8:38961910
|
A | G | 1 | a0002c0002t0004g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.837+4524A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38961910 | ||||||
chr8:38962007
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.837+4621A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962007 | ||||||
chr8:38962287
|
G | A | 12 | a0001c0001t0012g0139a0001c0001t0012g0182a0001c0001t0012g0184others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.837+4901G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962287 | ||||||
chr8:38962393
|
T | G | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837+5007T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962393 | ||||||
chr8:38962550
|
G | A | 1 | a0001c0001t0003g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.837+5164G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962550 | ||||||
chr8:38962590
|
A | G | 13 | a0001c0001t0012g0139a0001c0001t0012g0182a0001c0001t0012g0184others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+5204A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962590 | ||||||
chr8:38962630
|
A | C | 2 | a0001c0001t0032g0101a0001c0001t0045g0302 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.837+5244A>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962630 | ||||||
chr8:38962845
|
C | T | 179 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(176): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.837+5459C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962845 | ||||||
chr8:38962919
|
A | G | 163 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.837+5533A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38962919 | ||||||
chr8:38963050
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.838-5542A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963050 | ||||||
chr8:38963280
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.838-5312A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963280 | ||||||
chr8:38963403
|
A | T | 45 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0030others(42): Show | 46 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.838-5189A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963403 | ||||||
chr8:38963405
|
T | A | 2 | a0001c0001t0005g0174a0001c0001t0005g0192 | 2 | NA18992.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.838-5187T>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963405 | ||||||
chr8:38963452
|
G | A | 1 | a0001c0001t0005g0192 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.838-5140G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963452 | ||||||
chr8:38963612
|
G | A | 44 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0030others(41): Show | 45 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.838-4980G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963612 | ||||||
chr8:38963751
|
T | C | 44 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0030others(41): Show | 45 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.838-4841T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963751 | ||||||
chr8:38963809
|
A | G | 346 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(343): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.838-4783A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963809 | ||||||
chr8:38963856
|
G | A | 2 | a0001c0001t0009g0010a0001c0001t0009g0011 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.838-4736G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38963856 | ||||||
chr8:38964131
|
G | A | 1 | a0001c0001t0034g0181 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.838-4461G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964131 | ||||||
chr8:38964147
|
G | A | 180 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(177): Show | 181 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.838-4445G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964147 | ||||||
chr8:38964172
|
A | T | 130 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(127): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.838-4420A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964172 | ||||||
chr8:38964505
|
C | T | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.838-4087C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964505 | ||||||
chr8:38964516
|
G | A | 44 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0030others(41): Show | 45 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.838-4076G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964516 | ||||||
chr8:38964708
|
GA | G | 13 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0071others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-3874delA | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964708 | |||||
chr8:38964795
|
T | C | 47 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0030others(44): Show | 48 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.838-3797T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964795 | ||||||
chr8:38964817
|
A | T | 7 | a0001c0001t0001g0054a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 7 | HG01928.hp1 HG01934.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-3775A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38964817 | ||||||
chr8:38964852
|
C | CT | 92 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0037others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.838-3710dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38964852
|
C | CTT | 26 | a0001c0001t0001g0055a0001c0001t0001g0068a0001c0001t0001g0073others(23): Show | 26 | HG00673.hp1 HG01361.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.838-3711_838-3710d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38964852
|
CT | C | 37 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(34): Show | 37 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.838-3710delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38964852
|
CTT | C | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 67 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.838-3711_838-3710d others(4): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38964852
|
CTTT | C | 11 | a0001c0001t0001g0368a0001c0001t0003g0026a0001c0001t0012g0139others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.838-3712_838-3710d others(5): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38964852
|
CTTTTTTT | C | 6 | a0001c0001t0003g0034a0001c0001t0003g0172a0001c0001t0003g0299others(3): Show | 6 | HG01243.hp2 HG01884.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-3716_838-3710d others(9): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38964852
|
CTTTTTTT others(1): Show |
C | 40 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0030others(37): Show | 41 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.838-3717_838-3710d others(10): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38964852
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0007g0129a0001c0001t0007g0130a0001c0001t0016g0149others(2): Show | 5 | HG02622.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-3722_838-3710d others(15): Show |
PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38964852 | |||||
chr8:38965186
|
G | T | 1 | a0001c0001t0002g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.838-3406G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965186 | ||||||
chr8:38965293
|
G | A | 3 | a0001c0001t0016g0132a0001c0001t0018g0244a0001c0007t0016g0157 | 3 | HG02257.hp1 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.838-3299G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965293 | ||||||
chr8:38965763
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0354a0001c0001t0007g0300 | 3 | NA18995.hp1 NA19075.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.838-2829G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965763 | ||||||
chr8:38965993
|
C | G | 48 | a0001c0001t0001g0282a0001c0001t0003g0002a0001c0001t0003g0026others(45): Show | 49 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.838-2599C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38965993 | ||||||
chr8:38966378
|
A | T | 1 | a0001c0001t0001g0235 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.838-2214A>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966378 | ||||||
chr8:38966464
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.838-2128A>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966464 | ||||||
chr8:38966481
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(277): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.838-2111T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966481 | ||||||
chr8:38966542
|
T | C | 41 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0047others(38): Show | 41 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.838-2050T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966542 | ||||||
chr8:38966611
|
C | T | 1 | a0001c0001t0004g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.838-1981C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966611 | ||||||
chr8:38966733
|
G | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(273): Show | 278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.838-1859G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966733 | ||||||
chr8:38966903
|
G | A | 2 | a0001c0001t0020g0126a0001c0001t0050g0167 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.838-1689G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38966903 | ||||||
chr8:38967134
|
G | A | 2 | a0001c0001t0013g0117a0001c0001t0013g0152 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.838-1458G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967134 | ||||||
chr8:38967409
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0236 | 2 | NA19063.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.838-1183G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967409 | ||||||
chr8:38967664
|
C | CT | 17 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0368others(14): Show | 17 | HG02165.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.838-913dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 38967664 | |||||
chr8:38967696
|
C | T | 1 | a0001c0001t0034g0181 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.838-896C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967696 | ||||||
chr8:38967720
|
G | A | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.838-872G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967720 | ||||||
chr8:38967723
|
G | T | 1 | a0001c0001t0045g0302 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.838-869G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967723 | ||||||
chr8:38967733
|
C | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0236 | 2 | NA19063.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.838-859C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967733 | ||||||
chr8:38967952
|
C | G | 2 | a0001c0001t0003g0104a0001c0001t0013g0146 | 2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.838-640C>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38967952 | ||||||
chr8:38968035
|
C | T | 13 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0071others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-557C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38968035 | ||||||
chr8:38968183
|
T | C | 13 | a0001c0001t0009g0010a0001c0001t0009g0011a0001c0001t0009g0071others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-409T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 10/11 | chr8 | 38968183 | ||||||
chr8:38968691
|
G | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0368 | 3 | NA18946.hp2 NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.915+22G>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968691 | ||||||
chr8:38968692
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0368 | 3 | NA18946.hp2 NA19081.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.915+23C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968692 | ||||||
chr8:38968768
|
C | T | 5 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0067others(2): Show | 5 | HG01175.hp1 NA18948.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+99C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968768 | ||||||
chr8:38968772
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(255): Show | 260 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.915+103G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968772 | ||||||
chr8:38968847
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(272): Show | 277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.915+178T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968847 | ||||||
chr8:38968898
|
C | CT | 10 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0086others(7): Show | 10 | HG01255.hp2 HG01981.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.915+247dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 38968898 | |||||
chr8:38968898
|
CT | C | 12 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0251others(9): Show | 12 | HG01106.hp2 HG01358.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.915+247delT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 38968898 | |||||
chr8:38968938
|
G | A | 1 | a0001c0001t0009g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.915+269G>A | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968938 | ||||||
chr8:38968961
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.915+292C>T | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38968961 | ||||||
chr8:38969065
|
A | AT | 205 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(202): Show | 206 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.916-349dupT | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 38969065 | |||||
chr8:38969154
|
G | C | 2 | a0001c0001t0020g0126a0001c0001t0050g0167 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.916-267G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969154 | ||||||
chr8:38969250
|
G | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(203): Show | 207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.916-171G>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969250 | ||||||
chr8:38969274
|
T | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(273): Show | 278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.916-147T>G | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969274 | ||||||
chr8:38969367
|
T | C | 1 | a0001c0001t0001g0333 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.916-54T>C | PLEKHA2 | ENSG00000169499.15 | transcript | ENST00000617275.5 | protein_coding | 11/11 | chr8 | 38969367 |