geneid | 55124 |
---|---|
ensemblid | ENSG00000197181.12 |
hgncid | 17644 |
symbol | PIWIL2 |
name | piwi like RNA-mediated gene silencing 2 |
refseq_nuc | NM_018068.5 |
refseq_prot | NP_060538.2 |
ensembl_nuc | ENST00000356766.11 |
ensembl_prot | ENSP00000349208.6 |
mane_status | MANE Select |
chr | chr8 |
start | 22275316 |
end | 22357568 |
strand | + |
ver | v1.2 |
region | chr8:22275316-22357568 |
region5000 | chr8:22270316-22362568 |
regionname0 | PIWIL2_chr8_22275316_22357568 |
regionname5000 | PIWIL2_chr8_22270316_22362568 |
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 | 1/0 | 973 | 274 | 87 | 60 | 92 | 6 | 28 | 75 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0002 | 0/0 | 973 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0003 | 0/0 | 973 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0004 | 0/0 | 973 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0005 | 0/0 | 973 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0006 | 0/0 | 973 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0007 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0008 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0009 | 0/0 | 973 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0010 | 0/0 | 973 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0011 | 0/1 | 973 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
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 | 1/0 | 2922 | 273 | 87 | 59 | 92 | 6 | 28 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0002 | 0/0 | 2922 | 5 | 4 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0003 | 0/0 | 2922 | 5 | 0 | 0 | 5 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0004 | 0/0 | 2922 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0005 | 0/0 | 2922 | 2 | 0 | 0 | 2 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0006 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0007 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0008 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0009 | 0/1 | 2922 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0010 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0011 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
c0012 | 0/0 | 2922 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
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 | 2193 | 67 | 53 | 6 | 6 | 1 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0002 | 1/0 | 2193 | 63 | 11 | 21 | 26 | 1 | 3 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0003 | 0/0 | 2193 | 51 | 1 | 10 | 29 | 1 | 10 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0004 | 0/1 | 2191 | 49 | 4 | 12 | 24 | 0 | 8 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0005 | 0/0 | 2193 | 10 | 0 | 6 | 4 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0006 | 0/0 | 2193 | 8 | 4 | 2 | 0 | 0 | 2 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0007 | 0/0 | 2193 | 5 | 5 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0008 | 0/0 | 2193 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0009 | 0/0 | 2193 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0010 | 0/0 | 2192 | 4 | 0 | 0 | 3 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0011 | 0/0 | 2194 | 3 | 0 | 0 | 1 | 1 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0012 | 0/0 | 2193 | 3 | 2 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0013 | 0/0 | 2194 | 3 | 0 | 0 | 3 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0014 | 0/0 | 2193 | 3 | 3 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0015 | 0/0 | 2193 | 2 | 1 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0016 | 0/0 | 2194 | 2 | 1 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0017 | 0/0 | 2193 | 2 | 0 | 0 | 0 | 2 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0018 | 0/0 | 2194 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0019 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0020 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0021 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0022 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0023 | 0/0 | 2194 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0024 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0025 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0026 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0027 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0028 | 0/0 | 2191 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0029 | 0/0 | 2191 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
t0030 | 0/0 | 2191 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
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 | 1 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
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 | 1/0 | 2922 | 273 | 87 | 59 | 92 | 6 | 28 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0010 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0002c0003 | 0/0 | 2922 | 5 | 0 | 0 | 5 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0003c0002 | 0/0 | 2922 | 5 | 4 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0004c0004 | 0/0 | 2922 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0005c0005 | 0/0 | 2922 | 2 | 0 | 0 | 2 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0006c0012 | 0/0 | 2922 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0007c0011 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0008c0006 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0009c0007 | 0/0 | 2922 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0010c0008 | 0/0 | 2922 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0011c0009 | 0/1 | 2922 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5114 | 66 | 52 | 6 | 6 | 1 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0002 | 1/0 | 5114 | 60 | 11 | 21 | 23 | 1 | 3 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0003 | 0/0 | 5114 | 43 | 1 | 9 | 22 | 1 | 10 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0004 | 0/0 | 5112 | 47 | 4 | 11 | 24 | 0 | 8 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0005 | 0/0 | 5114 | 10 | 0 | 6 | 4 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0006 | 0/0 | 5114 | 8 | 4 | 2 | 0 | 0 | 2 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0007 | 0/0 | 5114 | 5 | 5 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0008 | 0/0 | 5114 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0010 | 0/0 | 5113 | 4 | 0 | 0 | 3 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0011 | 0/0 | 5115 | 3 | 0 | 0 | 1 | 1 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0013 | 0/0 | 5115 | 3 | 0 | 0 | 3 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0014 | 0/0 | 5114 | 3 | 3 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0015 | 0/0 | 5114 | 2 | 1 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0016 | 0/0 | 5115 | 2 | 1 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0017 | 0/0 | 5114 | 2 | 0 | 0 | 0 | 2 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0018 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0019 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0020 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0021 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0024 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0025 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0026 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0027 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0028 | 0/0 | 5112 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0029 | 0/0 | 5112 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0001t0030 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0001c0010t0003 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0002c0003t0003 | 0/0 | 5114 | 5 | 0 | 0 | 5 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0003c0002t0001 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0003c0002t0012 | 0/0 | 5114 | 3 | 2 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0003c0002t0022 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0004c0004t0009 | 0/0 | 5114 | 4 | 4 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0005c0005t0002 | 0/0 | 5114 | 2 | 0 | 0 | 2 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0006c0012t0023 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0007c0011t0003 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0008c0006t0002 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0009c0007t0003 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0010c0008t0004 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
a0011c0009t0004 | 0/1 | 5112 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | copy fasta | chr8 | 22270316 | 22362568 |
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 | 1 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0013g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0013g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0014g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0015g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0016g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0017g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0017g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0018g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0019g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0020g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0021g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0024g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0025g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0026g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0027g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0028g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0029g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0001t0030g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0001c0010t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0002c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0002c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0002c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0002c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0002c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0003c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0003c0002t0012g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0003c0002t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0003c0002t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0003c0002t0022g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0004c0004t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0004c0004t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0004c0004t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0004c0004t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0005c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0005c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0006c0012t0023g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0007c0011t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0008c0006t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0009c0007t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0010c0008t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
a0011c0009t0004g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00423 | hp1 | a0007 | c0011 | t0003 | g0281 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00597 | hp2 | a0002 | c0003 | t0003 | g0248 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | CHS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00639 | hp1 | a0001 | c0001 | t0030 | g0193 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00735 | hp1 | a0001 | c0001 | t0021 | g0030 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG00741 | hp2 | a0001 | c0001 | t0019 | g0077 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01099 | hp2 | a0003 | c0002 | t0012 | g0016 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0217 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0219 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01243 | hp2 | a0010 | c0008 | t0004 | g0231 | AMR | PUR | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01257 | hp2 | a0001 | c0010 | t0003 | g0173 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0189 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0227 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0221 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01496 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01516 | hp1 | a0001 | c0001 | t0011 | g0034 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01516 | hp2 | a0001 | c0001 | t0017 | g0282 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01517 | hp1 | a0001 | c0001 | t0017 | g0267 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01891 | hp1 | a0004 | c0004 | t0009 | g0176 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0038 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02027 | hp1 | a0009 | c0007 | t0003 | g0294 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02027 | hp2 | a0001 | c0001 | t0013 | g0240 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0116 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02056 | hp2 | a0001 | c0001 | t0020 | g0098 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0079 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02145 | hp2 | a0003 | c0002 | t0001 | g0019 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PEL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0295 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02602 | hp2 | a0001 | c0001 | t0010 | g0188 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0179 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02723 | hp1 | a0003 | c0002 | t0012 | g0017 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0186 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02895 | hp1 | a0004 | c0004 | t0009 | g0178 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02922 | hp1 | a0004 | c0004 | t0009 | g0177 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0159 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0162 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0184 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03017 | hp1 | a0001 | c0001 | t0018 | g0096 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03139 | hp2 | a0001 | c0001 | t0024 | g0158 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03486 | hp1 | a0003 | c0002 | t0012 | g0020 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03486 | hp2 | a0001 | c0001 | t0014 | g0185 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0198 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03579 | hp2 | a0003 | c0002 | t0022 | g0018 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03654 | hp1 | a0001 | c0001 | t0011 | g0081 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0201 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0285 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0197 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0181 | SAS | PJL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0220 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0268 | SAS | BEB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG04204 | hp1 | a0001 | c0001 | t0015 | g0073 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0199 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | STU | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | CHB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18959 | hp1 | a0001 | c0001 | t0013 | g0274 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18962 | hp1 | a0002 | c0003 | t0003 | g0250 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18962 | hp2 | a0005 | c0005 | t0002 | g0047 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18963 | hp1 | a0001 | c0001 | t0028 | g0252 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18972 | hp2 | a0005 | c0005 | t0002 | g0076 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18984 | hp1 | a0001 | c0001 | t0029 | g0202 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18985 | hp1 | a0001 | c0001 | t0016 | g0148 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18988 | hp2 | a0002 | c0003 | t0003 | g0249 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18989 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19001 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19009 | hp2 | a0001 | c0001 | t0027 | g0005 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0180 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19056 | hp2 | a0002 | c0003 | t0003 | g0244 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19058 | hp1 | a0001 | c0001 | t0026 | g0147 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19064 | hp1 | a0001 | c0001 | t0013 | g0273 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19067 | hp2 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19080 | hp2 | a0001 | c0001 | t0010 | g0230 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19081 | hp1 | a0008 | c0006 | t0002 | g0066 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19081 | hp2 | a0002 | c0003 | t0003 | g0245 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19090 | hp2 | a0001 | c0001 | t0011 | g0083 | EAS | JPT | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA20129 | hp1 | a0004 | c0004 | t0009 | g0174 | AFR | ASW | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | ASW | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0260 | EUR | TSI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01123 | hp1 | a0001 | c0001 | t0025 | g0172 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0107 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0164 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03471 | hp1 | a0006 | c0012 | t0023 | g0247 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | USA | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
homoSapiens_chm13v2 | hp1 | a0011 | c0009 | t0004 | g0207 | REF | REF | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0057 | REF | REF | PIWIL2_chr8_22270316_22362568 | PIWIL2 | chr8 | 22270316 | 22362568 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:22279558
|
A | G | 1 | a0006 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.172A>G | p.Ser58Gly | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/23 | 301/5114 | 172/2922 | 58/973 | chr8 | 22279558 | ||
chr8:22281440
|
C | G | 1 | a0002 | 5 | HG00597.hp2 NA18962.hp1 NA18988.hp2 others(2): Show |
missense_variant | MODERATE | c.350C>G | p.Ser117Cys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/23 | 479/5114 | 350/2922 | 117/973 | chr8 | 22281440 | ||
chr8:22283138
|
C | T | 1 | a0007 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.530C>T | p.Pro177Leu | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/23 | 659/5114 | 530/2922 | 177/973 | chr8 | 22283138 | ||
chr8:22283143
|
C | T | 1 | a0005 | 2 | NA18962.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.535C>T | p.Arg179Trp | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/23 | 664/5114 | 535/2922 | 179/973 | chr8 | 22283143 | ||
chr8:22287534
|
T | G | 1 | a0008 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.750T>G | p.Asn250Lys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/23 | 879/5114 | 750/2922 | 250/973 | chr8 | 22287534 | ||
chr8:22289899
|
A | G | 1 | a0005 | 2 | NA18962.hp2 NA18972.hp2 |
missense_variant | MODERATE | c.1039A>G | p.Thr347Ala | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 9/23 | 1168/5114 | 1039/2922 | 347/973 | chr8 | 22289899 | ||
chr8:22308039
|
G | A | 1 | a0009 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1652G>A | p.Arg551His | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/23 | 1781/5114 | 1652/2922 | 551/973 | chr8 | 22308039 | ||
chr8:22308068
|
C | T | 1 | a0003 | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
missense_variant | MODERATE | c.1681C>T | p.His561Tyr | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/23 | 1810/5114 | 1681/2922 | 561/973 | chr8 | 22308068 | ||
chr8:22311155
|
T | A | 1 | a0010 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1844T>A | p.Met615Lys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/23 | 1973/5114 | 1844/2922 | 615/973 | chr8 | 22311155 | ||
chr8:22311199
|
G | A | 1 | a0004 | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.1888G>A | p.Gly630Ser | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/23 | 2017/5114 | 1888/2922 | 630/973 | chr8 | 22311199 | ||
chr8:22315092
|
C | T | 1 | a0011 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.2155C>T | p.Leu719Phe | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/23 | 2284/5114 | 2155/2922 | 719/973 | chr8 | 22315092 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:22290314
|
G | A | 1 | a0006c0012 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1149G>A | p.Lys383Lys | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/23 | 1278/5114 | 1149/2922 | 383/973 | chr8 | 22290314 | ||
chr8:22307974
|
T | C | 1 | a0007c0011 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.1587T>C | p.His529His | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/23 | 1716/5114 | 1587/2922 | 529/973 | chr8 | 22307974 | ||
chr8:22311132
|
A | C | 1 | a0001c0010 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.1821A>C | p.Ala607Ala | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/23 | 1950/5114 | 1821/2922 | 607/973 | chr8 | 22311132 | ||
chr8:22316286
|
C | T | 1 | a0006c0012 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2250C>T | p.Pro750Pro | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/23 | 2379/5114 | 2250/2922 | 750/973 | chr8 | 22316286 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:22275324
|
C | T | 29 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(26): Show | 216 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(213): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-121C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/23 | chr8 | 22275324 | ||||||
chr8:22275351
|
CCT | C | 7 | a0001c0001t0004a0001c0001t0010a0001c0001t0028others(4): Show | 56 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-93_-92delCT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/23 | 4034 | chr8 | 22275351 | |||||
chr8:22355748
|
C | G | 1 | a0004c0004t0009 | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 243 | chr8 | 22355748 | |||||
chr8:22355788
|
T | A | 1 | a0001c0001t0015 | 2 | HG02145.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*283T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 283 | chr8 | 22355788 | |||||
chr8:22355914
|
T | C | 2 | a0003c0002t0012a0003c0002t0022 | 4 | HG01099.hp2 HG02723.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*409T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 409 | chr8 | 22355914 | |||||
chr8:22355996
|
C | T | 1 | a0001c0001t0007 | 5 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*491C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 491 | chr8 | 22355996 | |||||
chr8:22356062
|
A | G | 1 | a0001c0001t0021 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 557 | chr8 | 22356062 | |||||
chr8:22356071
|
C | CA | 6 | a0001c0001t0010a0001c0001t0011a0001c0001t0013others(3): Show | 14 | HG01516.hp1 HG02027.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*583dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 584 | INFO_REALIGN_3_PRIME | chr8 | 22356071 | ||||
chr8:22356171
|
C | T | 1 | a0001c0001t0020 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*666C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 666 | chr8 | 22356171 | |||||
chr8:22356246
|
T | C | 1 | a0001c0001t0028 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*741T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 741 | chr8 | 22356246 | |||||
chr8:22356357
|
G | A | 1 | a0001c0001t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 852 | chr8 | 22356357 | |||||
chr8:22356376
|
G | C | 1 | a0001c0001t0019 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*871G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 871 | chr8 | 22356376 | |||||
chr8:22356394
|
G | A | 2 | a0004c0004t0009a0006c0012t0023 | 5 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*889G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 889 | chr8 | 22356394 | |||||
chr8:22356698
|
G | A | 1 | a0001c0001t0018 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1193G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1193 | chr8 | 22356698 | |||||
chr8:22356779
|
A | G | 1 | a0003c0002t0022 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1274A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1274 | chr8 | 22356779 | |||||
chr8:22356840
|
C | T | 1 | a0001c0001t0030 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1335 | chr8 | 22356840 | |||||
chr8:22356851
|
G | C | 1 | a0001c0001t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1346 | chr8 | 22356851 | |||||
chr8:22356853
|
T | G | 2 | a0001c0001t0025a0001c0001t0029 | 2 | HG01123.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1348T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1348 | chr8 | 22356853 | |||||
chr8:22356861
|
C | T | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(15): Show | 125 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1356 | chr8 | 22356861 | |||||
chr8:22356995
|
T | C | 8 | a0001c0001t0001a0001c0001t0007a0001c0001t0016others(5): Show | 81 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1490T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1490 | chr8 | 22356995 | |||||
chr8:22357043
|
A | G | 1 | a0001c0001t0027 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1538A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1538 | chr8 | 22357043 | |||||
chr8:22357095
|
A | G | 1 | a0001c0001t0017 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1590A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1590 | chr8 | 22357095 | |||||
chr8:22357156
|
A | G | 1 | a0001c0001t0014 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1651A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1651 | chr8 | 22357156 | |||||
chr8:22357178
|
A | G | 1 | a0001c0001t0005 | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1673A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1673 | chr8 | 22357178 | |||||
chr8:22357487
|
C | A | 1 | a0001c0001t0026 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 23/23 | 1982 | chr8 | 22357487 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:22275410
|
C | A | 1 | a0001c0001t0003g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-47+12C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275410 | ||||||
chr8:22275507
|
T | C | 1 | a0001c0001t0004g0003 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-47+109T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275507 | ||||||
chr8:22275668
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0027g0005 | 2 | NA19009.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-47+270G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275668 | ||||||
chr8:22275802
|
C | T | 1 | a0001c0001t0006g0295 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-47+404C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275802 | ||||||
chr8:22275862
|
C | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+464C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275862 | ||||||
chr8:22275967
|
G | A | 4 | a0001c0001t0006g0021a0001c0001t0006g0022a0001c0001t0006g0023others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+569G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22275967 | ||||||
chr8:22276018
|
C | T | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+620C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276018 | ||||||
chr8:22276102
|
G | A | 1 | a0001c0001t0002g0025 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-47+704G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276102 | ||||||
chr8:22276231
|
C | T | 148 | a0001c0001t0001g0183a0001c0001t0001g0242a0001c0001t0001g0287others(145): Show | 148 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.-47+833C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276231 | ||||||
chr8:22276252
|
G | C | 1 | a0001c0001t0002g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-47+854G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276252 | ||||||
chr8:22276391
|
C | G | 7 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+993C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276391 | ||||||
chr8:22276509
|
G | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+1111G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276509 | ||||||
chr8:22276566
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-47+1168G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276566 | ||||||
chr8:22276656
|
T | C | 2 | a0003c0002t0012g0016a0003c0002t0012g0017 | 2 | HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-47+1258T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276656 | ||||||
chr8:22276711
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47+1313G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276711 | ||||||
chr8:22276742
|
T | C | 3 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0025g0172 | 3 | HG01070.hp1 HG01123.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-47+1344T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276742 | ||||||
chr8:22276904
|
TA | T | 160 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(157): Show | 160 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.-47+1518delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22276904 | |||||
chr8:22276989
|
G | A | 7 | a0001c0001t0007g0180a0001c0001t0008g0175a0001c0001t0008g0179others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+1591G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276989 | ||||||
chr8:22276997
|
G | A | 7 | a0001c0001t0007g0180a0001c0001t0008g0175a0001c0001t0008g0179others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+1599G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22276997 | ||||||
chr8:22277018
|
GAT | G | 6 | a0001c0001t0003g0256a0003c0002t0001g0019a0003c0002t0012g0016others(3): Show | 6 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+1635_-47+1636d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22277018 | |||||
chr8:22277028
|
TA | T | 44 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(41): Show | 44 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-47+1631delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277028 | ||||||
chr8:22277029
|
A | T | 1 | a0009c0007t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-47+1631A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277029 | ||||||
chr8:22277030
|
TA | T | 18 | a0001c0001t0006g0021a0001c0001t0006g0022a0001c0001t0006g0023others(15): Show | 18 | HG00597.hp2 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+1633delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277030 | ||||||
chr8:22277031
|
A | AT | 18 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0124others(15): Show | 18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+1634dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22277031 | |||||
chr8:22277031
|
A | T | 52 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(49): Show | 52 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-47+1633A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277031 | ||||||
chr8:22277032
|
TA | T | 18 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(15): Show | 18 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47+1635delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277032 | ||||||
chr8:22277033
|
A | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0102others(183): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.-47+1635A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277033 | ||||||
chr8:22277033
|
ATT | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+1645_-47+1646d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22277033 | |||||
chr8:22277035
|
T | A | 11 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0031others(8): Show | 11 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47+1637T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277035 | ||||||
chr8:22277037
|
T | A | 1 | a0001c0001t0005g0006 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47+1639T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277037 | ||||||
chr8:22277049
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02055.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1651C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277049 | ||||||
chr8:22277059
|
T | C | 7 | a0001c0001t0001g0163a0001c0001t0024g0158a0003c0002t0001g0019others(4): Show | 7 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+1661T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277059 | ||||||
chr8:22277140
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+1742G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277140 | ||||||
chr8:22277313
|
T | C | 90 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0183others(87): Show | 90 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.-47+1915T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277313 | ||||||
chr8:22277568
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG00733.hp1 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-1773C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277568 | ||||||
chr8:22277704
|
A | G | 1 | a0001c0001t0004g0246 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-46-1637A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277704 | ||||||
chr8:22277821
|
A | C | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-1520A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277821 | ||||||
chr8:22277852
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(47): Show | 51 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.-46-1489A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277852 | ||||||
chr8:22277875
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-46-1466A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277875 | ||||||
chr8:22277967
|
G | C | 1 | a0001c0001t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-46-1374G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277967 | ||||||
chr8:22277998
|
G | A | 1 | a0001c0001t0004g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-46-1343G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22277998 | ||||||
chr8:22278066
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-46-1275G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278066 | ||||||
chr8:22278177
|
A | G | 59 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0287others(56): Show | 59 | HG00423.hp1 HG00558.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.-46-1164A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278177 | ||||||
chr8:22278498
|
C | T | 1 | a0001c0001t0004g0243 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-46-843C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278498 | ||||||
chr8:22278595
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-46-746T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278595 | ||||||
chr8:22278851
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-46-490C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22278851 | ||||||
chr8:22279080
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-46-261C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | chr8 | 22279080 | ||||||
chr8:22279108
|
TC | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46-231delC | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | 22279108 | |||||
chr8:22279758
|
G | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.198+174G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279758 | ||||||
chr8:22279812
|
C | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.198+228C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279812 | ||||||
chr8:22279825
|
C | T | 1 | a0001c0001t0003g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.198+241C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279825 | ||||||
chr8:22279897
|
C | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+313C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279897 | ||||||
chr8:22279913
|
C | T | 2 | a0001c0001t0002g0085a0006c0012t0023g0247 | 2 | HG03471.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.198+329C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22279913 | ||||||
chr8:22280002
|
G | A | 122 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(119): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.198+418G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280002 | ||||||
chr8:22280088
|
G | C | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.198+504G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280088 | ||||||
chr8:22280164
|
C | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(13): Show | 17 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+580C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280164 | ||||||
chr8:22280212
|
A | T | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.198+628A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280212 | ||||||
chr8:22280366
|
G | A | 1 | a0001c0001t0004g0251 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.199-754G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280366 | ||||||
chr8:22280498
|
C | T | 1 | a0001c0001t0004g0003 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.199-622C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280498 | ||||||
chr8:22280671
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199-449A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280671 | ||||||
chr8:22280686
|
T | G | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199-434T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280686 | ||||||
chr8:22280715
|
A | G | 11 | a0001c0001t0001g0163a0001c0001t0005g0006a0001c0001t0005g0007others(8): Show | 11 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-405A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280715 | ||||||
chr8:22280771
|
AGTTCTGT others(48): Show |
A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-302_199-248del others(55): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | 22280771 | |||||
chr8:22280993
|
G | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-127G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22280993 | ||||||
chr8:22281063
|
C | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG00741.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.199-57C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 2/22 | chr8 | 22281063 | ||||||
chr8:22281307
|
A | T | 7 | a0001c0001t0008g0175a0001c0001t0008g0179a0001c0001t0014g0186others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-70A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 3/22 | chr8 | 22281307 | ||||||
chr8:22281334
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.287-43G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 3/22 | chr8 | 22281334 | ||||||
chr8:22281342
|
C | T | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-35C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 3/22 | chr8 | 22281342 | ||||||
chr8:22281657
|
A | G | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.425+142A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281657 | ||||||
chr8:22281685
|
T | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.425+170T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281685 | ||||||
chr8:22281767
|
A | AT | 34 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0152others(31): Show | 34 | HG00408.hp1 HG00597.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.425+274dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22281767 | |||||
chr8:22281767
|
AT | A | 15 | a0001c0001t0001g0123a0001c0001t0005g0006a0001c0001t0005g0007others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.425+274delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22281767 | |||||
chr8:22281841
|
G | C | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.425+326G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281841 | ||||||
chr8:22281847
|
C | T | 2 | a0001c0001t0014g0185a0001c0001t0014g0186 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.425+332C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281847 | ||||||
chr8:22281876
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425+361A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22281876 | ||||||
chr8:22282074
|
C | CT | 143 | a0001c0001t0001g0125a0001c0001t0001g0142a0001c0001t0001g0146others(140): Show | 143 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.425+581dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282074 | |||||
chr8:22282074
|
C | CTT | 57 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(54): Show | 58 | HG00738.hp2 HG01175.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.425+580_425+581dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282074 | |||||
chr8:22282074
|
C | CTTTTT | 11 | a0001c0001t0005g0006a0001c0001t0005g0008a0001c0001t0005g0009others(8): Show | 11 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.425+577_425+581dup others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282074 | |||||
chr8:22282191
|
C | G | 1 | a0001c0001t0003g0286 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.425+676C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282191 | ||||||
chr8:22282222
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.425+707A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282222 | ||||||
chr8:22282229
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0003g0285 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.425+714C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282229 | ||||||
chr8:22282244
|
C | CT | 34 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(31): Show | 34 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.425+756dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | |||||
chr8:22282244
|
C | CTT | 9 | a0001c0001t0001g0154a0001c0001t0002g0078a0001c0001t0002g0082others(6): Show | 9 | HG00741.hp2 HG01175.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.425+755_425+756dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | |||||
chr8:22282244
|
CT | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.425+756delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | |||||
chr8:22282244
|
CTT | C | 32 | a0001c0001t0001g0183a0001c0001t0003g0225a0001c0001t0003g0239others(29): Show | 32 | HG00423.hp1 HG00735.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.425+755_425+756del others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | |||||
chr8:22282244
|
CTTT | C | 94 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(91): Show | 94 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.425+754_425+756del others(3): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282244 | |||||
chr8:22282316
|
A | ATCTTGG | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(1): Show | 4 | HG01099.hp1 HG01934.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-717_426-712dup others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr8 | 22282316 | |||||
chr8:22282320
|
T | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.426-714T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282320 | ||||||
chr8:22282470
|
G | A | 4 | a0001c0001t0005g0008a0001c0001t0005g0009a0001c0001t0005g0010others(1): Show | 4 | NA18942.hp1 NA18959.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-564G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282470 | ||||||
chr8:22282473
|
C | T | 1 | a0001c0001t0010g0233 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.426-561C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282473 | ||||||
chr8:22282894
|
C | T | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-140C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 4/22 | chr8 | 22282894 | ||||||
chr8:22283250
|
G | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.632+10G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283250 | ||||||
chr8:22283431
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.632+191C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283431 | ||||||
chr8:22283448
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.632+208G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283448 | ||||||
chr8:22283499
|
C | T | 4 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0234others(1): Show | 4 | HG01361.hp2 HG02056.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.632+259C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283499 | ||||||
chr8:22283583
|
G | C | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.632+343G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283583 | ||||||
chr8:22283958
|
A | C | 2 | a0001c0001t0003g0290a0001c0001t0003g0291 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.633-204A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22283958 | ||||||
chr8:22284011
|
G | GT | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.633-150dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr8 | 22284011 | |||||
chr8:22284098
|
T | C | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.633-64T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 5/22 | chr8 | 22284098 | ||||||
chr8:22284294
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.743+22A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284294 | ||||||
chr8:22284398
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.743+126C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284398 | ||||||
chr8:22284468
|
C | T | 1 | a0001c0001t0014g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.743+196C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284468 | ||||||
chr8:22284498
|
A | C | 5 | a0001c0001t0004g0216a0001c0001t0004g0217a0001c0001t0004g0218others(2): Show | 5 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+226A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284498 | ||||||
chr8:22284565
|
C | G | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.743+293C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284565 | ||||||
chr8:22284565
|
C | T | 6 | a0001c0001t0008g0175a0001c0001t0008g0179a0004c0004t0009g0174others(3): Show | 6 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+293C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284565 | ||||||
chr8:22284582
|
G | C | 1 | a0001c0001t0014g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.743+310G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284582 | ||||||
chr8:22284665
|
T | C | 4 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0040others(1): Show | 4 | HG01496.hp1 HG01975.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+393T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284665 | ||||||
chr8:22284685
|
G | A | 6 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0011others(3): Show | 6 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+413G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284685 | ||||||
chr8:22284901
|
G | A | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+629G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284901 | ||||||
chr8:22284980
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743+708A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22284980 | ||||||
chr8:22285248
|
G | A | 4 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0260others(1): Show | 4 | HG00735.hp2 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+976G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285248 | ||||||
chr8:22285599
|
T | C | 2 | a0001c0001t0002g0028a0001c0001t0002g0029 | 2 | NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.743+1327T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285599 | ||||||
chr8:22285644
|
C | A | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+1372C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285644 | ||||||
chr8:22285834
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.743+1562G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22285834 | ||||||
chr8:22286197
|
ATCT | A | 8 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 8 | HG02004.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.744-1327_744-1325d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 22286197 | |||||
chr8:22286217
|
C | T | 2 | a0001c0001t0014g0185a0001c0001t0014g0186 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-1311C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286217 | ||||||
chr8:22286435
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.744-1093G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286435 | ||||||
chr8:22286438
|
A | T | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.744-1090A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286438 | ||||||
chr8:22286804
|
A | C | 1 | a0001c0001t0001g0027 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.744-724A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286804 | ||||||
chr8:22286999
|
C | T | 6 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0011others(3): Show | 6 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-529C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22286999 | ||||||
chr8:22287084
|
C | CA | 16 | a0001c0001t0003g0261a0001c0001t0005g0006a0001c0001t0005g0007others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.744-433dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | 22287084 | |||||
chr8:22287201
|
G | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.744-327G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22287201 | ||||||
chr8:22287428
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(1): Show | 4 | HG02965.hp2 HG03209.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-100T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 6/22 | chr8 | 22287428 | ||||||
chr8:22287806
|
G | A | 25 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0127others(22): Show | 25 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.861+161G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22287806 | ||||||
chr8:22288059
|
G | A | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.861+414G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288059 | ||||||
chr8:22288072
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.861+427G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288072 | ||||||
chr8:22288175
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.862-367G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288175 | ||||||
chr8:22288215
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.862-327G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288215 | ||||||
chr8:22288273
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.862-269G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | chr8 | 22288273 | ||||||
chr8:22288298
|
C | CA | 24 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0126others(21): Show | 24 | HG00639.hp2 HG00741.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.862-224dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr8 | 22288298 | |||||
chr8:22288298
|
C | CAA | 116 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0045others(113): Show | 116 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.862-225_862-224dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr8 | 22288298 | |||||
chr8:22288298
|
C | CAAA | 30 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0127others(27): Show | 30 | HG00423.hp1 HG00597.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.862-226_862-224dup others(3): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr8 | 22288298 | |||||
chr8:22288872
|
G | A | 119 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.986+206G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22288872 | ||||||
chr8:22288922
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.986+256A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22288922 | ||||||
chr8:22289099
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.986+433C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289099 | ||||||
chr8:22289152
|
C | CT | 15 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0003g0237others(12): Show | 15 | HG01074.hp2 HG01993.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.986+503dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr8 | 22289152 | |||||
chr8:22289152
|
CT | C | 19 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(16): Show | 19 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.986+503delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr8 | 22289152 | |||||
chr8:22289168
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.986+502T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289168 | ||||||
chr8:22289192
|
C | T | 3 | a0001c0001t0003g0263a0001c0001t0003g0286a0001c0001t0003g0293 | 3 | NA18984.hp2 NA19060.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.986+526C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289192 | ||||||
chr8:22289196
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.986+530A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289196 | ||||||
chr8:22289213
|
C | T | 1 | a0008c0006t0002g0066 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.986+547C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289213 | ||||||
chr8:22289233
|
A | G | 5 | a0001c0001t0002g0026a0001c0001t0002g0062a0001c0001t0002g0063others(2): Show | 5 | HG01069.hp1 HG01255.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+567A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289233 | ||||||
chr8:22289447
|
G | A | 2 | a0001c0001t0005g0007a0001c0001t0005g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.987-400G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289447 | ||||||
chr8:22289536
|
A | T | 1 | a0001c0001t0004g0192 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.987-311A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289536 | ||||||
chr8:22289551
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.987-296A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289551 | ||||||
chr8:22289712
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.987-135T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289712 | ||||||
chr8:22289731
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.987-116A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289731 | ||||||
chr8:22289820
|
A | G | 137 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(134): Show | 137 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.987-27A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 8/22 | chr8 | 22289820 | ||||||
chr8:22290572
|
G | A | 126 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0045others(123): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1181+226G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290572 | ||||||
chr8:22290583
|
G | A | 1 | a0001c0001t0003g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1181+237G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290583 | ||||||
chr8:22290613
|
A | AT | 102 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(99): Show | 102 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1181+288dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290613 | |||||
chr8:22290613
|
AT | A | 17 | a0001c0001t0002g0097a0001c0001t0003g0293a0001c0001t0005g0006others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1181+288delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290613 | |||||
chr8:22290613
|
ATTTTTTT | A | 7 | a0001c0001t0001g0106a0001c0001t0002g0031a0001c0001t0002g0032others(4): Show | 7 | HG00738.hp1 HG01255.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+282_1181+288d others(9): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290613 | |||||
chr8:22290974
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0005g0014 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1181+629_1181+630i others(58): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290974
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0005g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1181+629_1181+630i others(54): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290974
|
A | ATATATAT others(44): Show |
1 | a0001c0001t0005g0008 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1181+629_1181+630i others(53): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290974
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0005g0011 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1181+629_1181+630i others(47): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290974
|
A | ATATATAT others(39): Show |
2 | a0001c0001t0005g0006a0001c0001t0005g0012 | 2 | HG01258.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1181+629_1181+630i others(48): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290974
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0005g0013 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1181+629_1181+630i others(47): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290974
|
A | ATATATAT others(40): Show |
1 | a0001c0001t0005g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1181+629_1181+630i others(49): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290974
|
A | ATATATAT others(36): Show |
2 | a0001c0001t0005g0007a0001c0001t0005g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1181+629_1181+630i others(45): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22290974 | |||||
chr8:22290976
|
T | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1181+630T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290976 | ||||||
chr8:22290983
|
A | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+637A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290983 | ||||||
chr8:22290984
|
A | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+638A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290984 | ||||||
chr8:22290992
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+646A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22290992 | ||||||
chr8:22291000
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+654A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291000 | ||||||
chr8:22291005
|
A | G | 25 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0144others(22): Show | 25 | HG00597.hp1 HG00639.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1181+659A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291005 | ||||||
chr8:22291008
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+662A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291008 | ||||||
chr8:22291160
|
T | C | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1181+814T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291160 | ||||||
chr8:22291172
|
A | G | 7 | a0001c0001t0008g0175a0001c0001t0008g0179a0004c0004t0009g0174others(4): Show | 7 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+826A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291172 | ||||||
chr8:22291352
|
T | C | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+1006T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291352 | ||||||
chr8:22291497
|
T | C | 1 | a0001c0001t0006g0295 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1181+1151T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291497 | ||||||
chr8:22291551
|
A | G | 2 | a0001c0001t0002g0060a0001c0001t0002g0061 | 2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1181+1205A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291551 | ||||||
chr8:22291609
|
A | C | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1181+1263A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291609 | ||||||
chr8:22291727
|
C | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+1381C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291727 | ||||||
chr8:22291788
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+1442A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291788 | ||||||
chr8:22291927
|
G | A | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+1581G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291927 | ||||||
chr8:22291960
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1181+1614C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291960 | ||||||
chr8:22291963
|
A | G | 12 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(9): Show | 12 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1181+1617A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22291963 | ||||||
chr8:22292030
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1181+1684G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292030 | ||||||
chr8:22292059
|
A | T | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+1713A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292059 | ||||||
chr8:22292279
|
GT | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+1935delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22292279 | |||||
chr8:22292380
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1181+2034A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292380 | ||||||
chr8:22292394
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+2048G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292394 | ||||||
chr8:22292403
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1181+2057G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292403 | ||||||
chr8:22292467
|
C | T | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1181+2121C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292467 | ||||||
chr8:22292534
|
A | G | 8 | a0001c0001t0001g0183a0001c0001t0008g0175a0001c0001t0008g0179others(5): Show | 8 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1181+2188A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292534 | ||||||
chr8:22292754
|
G | A | 1 | a0001c0001t0014g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1181+2408G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292754 | ||||||
chr8:22292974
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1181+2628A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22292974 | ||||||
chr8:22293008
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1181+2662G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293008 | ||||||
chr8:22293017
|
C | G | 6 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 6 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+2671C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293017 | ||||||
chr8:22293060
|
A | G | 1 | a0001c0001t0004g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1181+2714A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293060 | ||||||
chr8:22293337
|
C | CAT | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+2991_1181+299 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293337 | ||||||
chr8:22293338
|
T | A | 138 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(135): Show | 138 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.1181+2992T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293338 | ||||||
chr8:22293798
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+3452A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22293798 | ||||||
chr8:22294020
|
G | A | 23 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0142others(20): Show | 23 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1181+3674G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294020 | ||||||
chr8:22294109
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1181+3763G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294109 | ||||||
chr8:22294148
|
G | T | 23 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0142others(20): Show | 23 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1181+3802G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294148 | ||||||
chr8:22294210
|
C | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0125others(14): Show | 17 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1181+3864C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294210 | ||||||
chr8:22294336
|
T | TA | 125 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(122): Show | 125 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1181+4012dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294336 | |||||
chr8:22294337
|
A | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1181+3991A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294337 | ||||||
chr8:22294363
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1181+4017C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294363 | ||||||
chr8:22294421
|
C | A | 1 | a0001c0001t0006g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1181+4075C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294421 | ||||||
chr8:22294434
|
G | A | 30 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0144others(27): Show | 30 | HG00597.hp1 HG00639.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1181+4088G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294434 | ||||||
chr8:22294502
|
G | A | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1181+4156G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294502 | ||||||
chr8:22294510
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1181+4164G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294510 | ||||||
chr8:22294644
|
C | CA | 41 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0114others(38): Show | 42 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1181+4322dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294644 | |||||
chr8:22294644
|
CA | C | 30 | a0001c0001t0001g0105a0001c0001t0001g0123a0001c0001t0001g0124others(27): Show | 30 | HG01069.hp1 HG01109.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1181+4322delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294644 | |||||
chr8:22294672
|
A | G | 6 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0011others(3): Show | 6 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181+4326A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294672 | ||||||
chr8:22294805
|
C | T | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+4459C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294805 | ||||||
chr8:22294825
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1181+4479C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294825 | ||||||
chr8:22294847
|
G | A | 1 | a0001c0001t0006g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1181+4501G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294847 | ||||||
chr8:22294894
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(291): Show | 295 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.1181+4548T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294894 | ||||||
chr8:22294898
|
TG | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0133a0004c0004t0009g0178others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+4554delG | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294898 | |||||
chr8:22294899
|
G | GA | 20 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(17): Show | 20 | HG01891.hp1 HG02004.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | ||||||
chr8:22294899
|
G | GAA | 71 | a0001c0001t0001g0119a0001c0001t0001g0157a0001c0001t0001g0287others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | ||||||
chr8:22294899
|
G | GAAA | 49 | a0001c0001t0001g0288a0001c0001t0003g0086a0001c0001t0003g0225others(46): Show | 49 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | ||||||
chr8:22294899
|
G | GAAAA | 4 | a0001c0001t0003g0196a0001c0001t0003g0239a0001c0001t0003g0289others(1): Show | 4 | HG01175.hp1 HG02027.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+4553_1181+455 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | ||||||
chr8:22294899
|
GGA | G | 7 | a0001c0001t0001g0183a0001c0001t0005g0006a0001c0001t0005g0007others(4): Show | 7 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+4554_1181+455 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | ||||||
chr8:22294899
|
GGAAAAAA others(5): Show |
G | 1 | a0001c0001t0003g0278 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1181+4554_1181+456 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | ||||||
chr8:22294899
|
GGAAAAAA others(6): Show |
G | 2 | a0001c0001t0001g0134a0001c0001t0008g0184 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1181+4554_1181+456 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294899 | ||||||
chr8:22294900
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(167): Show | 171 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.1181+4554G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294900 | ||||||
chr8:22294900
|
G | GA | 18 | a0001c0001t0001g0124a0001c0001t0001g0135a0001c0001t0001g0146others(15): Show | 18 | HG01123.hp2 HG02074.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1181+4583dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | |||||
chr8:22294900
|
GAAAAAAA others(4): Show |
G | 2 | a0001c0001t0002g0048a0001c0001t0002g0056 | 2 | NA18952.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1181+4573_1181+458 others(15): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | |||||
chr8:22294900
|
GAAAAAAA others(5): Show |
G | 2 | a0001c0001t0006g0023a0001c0001t0006g0024 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1181+4572_1181+458 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | |||||
chr8:22294900
|
GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1181+4571_1181+458 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22294900 | |||||
chr8:22294901
|
A | G | 1 | a0005c0005t0002g0047 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1181+4555A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294901 | ||||||
chr8:22294954
|
C | T | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1181+4608C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294954 | ||||||
chr8:22294995
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0003g0285 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1181+4649C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22294995 | ||||||
chr8:22295028
|
G | A | 127 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(124): Show | 127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1181+4682G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295028 | ||||||
chr8:22295184
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1181+4838A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295184 | ||||||
chr8:22295205
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1181+4859C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295205 | ||||||
chr8:22295337
|
C | CT | 178 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(175): Show | 179 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.1181+5001dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22295337 | |||||
chr8:22295356
|
G | A | 2 | a0001c0001t0001g0183a0006c0012t0023g0247 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1181+5010G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295356 | ||||||
chr8:22295472
|
A | G | 3 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0025g0172 | 3 | HG01070.hp1 HG01123.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1181+5126A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295472 | ||||||
chr8:22295580
|
C | CT | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+5235dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22295580 | |||||
chr8:22295683
|
C | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+5337C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295683 | ||||||
chr8:22295723
|
A | G | 127 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(124): Show | 127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1181+5377A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295723 | ||||||
chr8:22295750
|
A | G | 1 | a0001c0001t0015g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1181+5404A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295750 | ||||||
chr8:22295760
|
G | C | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1181+5414G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295760 | ||||||
chr8:22295868
|
G | A | 127 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(124): Show | 127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1181+5522G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295868 | ||||||
chr8:22295916
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1181+5570C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295916 | ||||||
chr8:22295964
|
G | T | 59 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(56): Show | 59 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1181+5618G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22295964 | ||||||
chr8:22296020
|
C | CT | 20 | a0001c0001t0002g0041a0001c0001t0002g0046a0001c0001t0002g0055others(17): Show | 20 | HG00733.hp2 HG00741.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1181+5712dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CT | C | 22 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0001g0169others(19): Show | 22 | HG00738.hp1 HG01099.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1181+5712delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0100 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1181+5702_1181+571 others(15): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0143a0003c0002t0001g0019 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1181+5700_1181+571 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CTTTTTTT others(7): Show |
C | 25 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(22): Show | 25 | HG00597.hp1 HG00639.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1181+5699_1181+571 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0005g0010others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+5698_1181+571 others(19): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0003g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1181+5692_1181+571 others(25): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CTTTTTTT others(15): Show |
C | 168 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(165): Show | 169 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.1181+5691_1181+571 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296020
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0004g0214 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1181+5690_1181+571 others(27): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296020 | |||||
chr8:22296022
|
T | C | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1181+5676T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296022 | ||||||
chr8:22296037
|
TTTTTTTT others(15): Show |
T | 2 | a0001c0001t0001g0163a0001c0001t0014g0185 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1181+5694_1181+571 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296037 | |||||
chr8:22296038
|
TTTTTTTT others(14): Show |
T | 1 | a0001c0001t0014g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1181+5695_1181+571 others(25): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22296038 | |||||
chr8:22296050
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1181+5704T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296050 | ||||||
chr8:22296053
|
T | G | 6 | a0001c0001t0001g0142a0001c0001t0001g0167a0001c0001t0001g0183others(3): Show | 6 | HG01099.hp1 HG01934.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181+5707T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296053 | ||||||
chr8:22296056
|
T | G | 29 | a0001c0001t0001g0142a0001c0001t0001g0165a0001c0001t0001g0166others(26): Show | 29 | HG00423.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1181+5710T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296056 | ||||||
chr8:22296056
|
T | TG | 6 | a0001c0001t0001g0168a0001c0001t0002g0042a0001c0001t0008g0179others(3): Show | 6 | HG00733.hp1 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181+5710_1181+571 others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296056 | ||||||
chr8:22296059
|
G | T | 1 | a0001c0001t0019g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1181+5713G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296059 | ||||||
chr8:22296083
|
T | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(39): Show | 43 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1181+5737T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296083 | ||||||
chr8:22296124
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1181+5778C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296124 | ||||||
chr8:22296135
|
A | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(170): Show | 174 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.1181+5789A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296135 | ||||||
chr8:22296250
|
T | A | 1 | a0001c0001t0004g0003 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1181+5904T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296250 | ||||||
chr8:22296260
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(182): Show | 186 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.1181+5914C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296260 | ||||||
chr8:22296319
|
A | G | 1 | a0001c0001t0003g0277 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1181+5973A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296319 | ||||||
chr8:22296337
|
G | A | 4 | a0001c0001t0003g0266a0001c0001t0003g0269a0001c0001t0003g0270others(1): Show | 4 | NA18940.hp1 NA18964.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+5991G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296337 | ||||||
chr8:22296367
|
A | G | 1 | a0001c0001t0025g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1181+6021A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296367 | ||||||
chr8:22296401
|
T | A | 1 | a0001c0001t0003g0286 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1181+6055T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296401 | ||||||
chr8:22296620
|
T | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(170): Show | 174 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.1181+6274T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296620 | ||||||
chr8:22296933
|
CA | C | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+6588delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296933 | ||||||
chr8:22296981
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1181+6635T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22296981 | ||||||
chr8:22297100
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1181+6754C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297100 | ||||||
chr8:22297365
|
T | C | 1 | a0001c0001t0002g0025 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1182-6656T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297365 | ||||||
chr8:22297367
|
T | G | 8 | a0001c0001t0001g0183a0001c0001t0008g0175a0001c0001t0008g0179others(5): Show | 8 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182-6654T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297367 | ||||||
chr8:22297507
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1182-6514C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297507 | ||||||
chr8:22297592
|
A | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-6429A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297592 | ||||||
chr8:22297608
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-6413A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297608 | ||||||
chr8:22297621
|
C | T | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1182-6400C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22297621 | ||||||
chr8:22298169
|
A | G | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1182-5852A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298169 | ||||||
chr8:22298273
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(184): Show | 188 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.1182-5748G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298273 | ||||||
chr8:22298398
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1182-5623G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298398 | ||||||
chr8:22298527
|
A | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-5494A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298527 | ||||||
chr8:22298572
|
A | G | 1 | a0001c0001t0028g0252 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1182-5449A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298572 | ||||||
chr8:22298680
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1182-5341C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298680 | ||||||
chr8:22298803
|
A | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-5218A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298803 | ||||||
chr8:22298957
|
G | C | 1 | a0001c0001t0015g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1182-5064G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22298957 | ||||||
chr8:22299013
|
T | C | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1182-5008T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299013 | ||||||
chr8:22299155
|
G | T | 1 | a0001c0001t0004g0190 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1182-4866G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299155 | ||||||
chr8:22299157
|
A | T | 62 | a0001c0001t0002g0045a0001c0001t0003g0196a0001c0001t0003g0225others(59): Show | 62 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1182-4864A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299157 | ||||||
chr8:22299314
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-4707G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299314 | ||||||
chr8:22299675
|
C | T | 4 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0279others(1): Show | 4 | HG01070.hp1 HG01074.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-4346C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299675 | ||||||
chr8:22299755
|
G | A | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-4266G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299755 | ||||||
chr8:22299825
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1182-4196T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299825 | ||||||
chr8:22299887
|
A | T | 1 | a0001c0001t0004g0212 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1182-4134A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299887 | ||||||
chr8:22299901
|
G | A | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182-4120G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299901 | ||||||
chr8:22299954
|
G | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG02886.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1182-4067G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22299954 | ||||||
chr8:22300004
|
A | G | 1 | a0001c0001t0003g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1182-4017A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300004 | ||||||
chr8:22300067
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(13): Show | 17 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1182-3954C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300067 | ||||||
chr8:22300102
|
A | AT | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-3911dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22300102 | |||||
chr8:22300178
|
A | G | 1 | a0001c0001t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1182-3843A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300178 | ||||||
chr8:22300305
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1182-3716G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300305 | ||||||
chr8:22300337
|
G | C | 1 | a0001c0001t0004g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1182-3684G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300337 | ||||||
chr8:22300438
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-3583G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300438 | ||||||
chr8:22300539
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1182-3482C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300539 | ||||||
chr8:22300635
|
A | G | 1 | a0001c0001t0003g0195 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1182-3386A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300635 | ||||||
chr8:22300637
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(220): Show | 224 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(221): Show |
intron_variant | MODIFIER | c.1182-3384A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300637 | ||||||
chr8:22300659
|
A | G | 7 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182-3362A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22300659 | ||||||
chr8:22300991
|
CT | C | 182 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0127others(179): Show | 182 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.1182-3019delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22300991 | |||||
chr8:22300991
|
CTT | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(37): Show | 41 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1182-3020_1182-301 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22300991 | |||||
chr8:22301102
|
C | T | 1 | a0001c0001t0004g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1182-2919C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301102 | ||||||
chr8:22301157
|
T | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(182): Show | 186 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.1182-2864T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301157 | ||||||
chr8:22301238
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1182-2783C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301238 | ||||||
chr8:22301330
|
G | T | 1 | a0003c0002t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1182-2691G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301330 | ||||||
chr8:22301403
|
C | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-2618C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301403 | ||||||
chr8:22301532
|
G | T | 1 | a0001c0001t0002g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1182-2489G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301532 | ||||||
chr8:22301589
|
C | T | 3 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0013g0240 | 3 | HG01175.hp1 HG02027.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1182-2432C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301589 | ||||||
chr8:22301726
|
G | GT | 134 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(131): Show | 134 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.1182-2284dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | 22301726 | |||||
chr8:22301770
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0152others(3): Show | 6 | NA18977.hp2 NA18985.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-2251C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301770 | ||||||
chr8:22301917
|
A | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-2104A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22301917 | ||||||
chr8:22302081
|
C | A | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1182-1940C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302081 | ||||||
chr8:22302107
|
A | C | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-1914A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302107 | ||||||
chr8:22302167
|
A | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(291): Show | 295 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.1182-1854A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302167 | ||||||
chr8:22302195
|
T | C | 1 | a0001c0001t0015g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1182-1826T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302195 | ||||||
chr8:22302214
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1182-1807G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302214 | ||||||
chr8:22302242
|
C | T | 1 | a0001c0001t0015g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1182-1779C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302242 | ||||||
chr8:22302282
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-1739A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302282 | ||||||
chr8:22302430
|
C | T | 3 | a0001c0001t0004g0253a0001c0001t0010g0188a0001c0001t0030g0193 | 3 | HG00639.hp1 HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1182-1591C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302430 | ||||||
chr8:22302465
|
T | C | 6 | a0001c0001t0001g0156a0001c0001t0002g0037a0004c0004t0009g0174others(3): Show | 6 | HG00597.hp1 HG00741.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-1556T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302465 | ||||||
chr8:22302552
|
C | T | 1 | a0003c0002t0012g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1182-1469C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302552 | ||||||
chr8:22302553
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1182-1468G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302553 | ||||||
chr8:22302693
|
A | C | 1 | a0001c0001t0011g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1182-1328A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22302693 | ||||||
chr8:22303086
|
G | T | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1182-935G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303086 | ||||||
chr8:22303257
|
A | G | 1 | a0001c0001t0003g0261 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1182-764A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303257 | ||||||
chr8:22303352
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-669A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303352 | ||||||
chr8:22303417
|
G | C | 16 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1182-604G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303417 | ||||||
chr8:22303571
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1182-450T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303571 | ||||||
chr8:22303666
|
C | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(46): Show | 50 | HG00733.hp1 HG00738.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.1182-355C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303666 | ||||||
chr8:22303859
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1182-162G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 10/22 | chr8 | 22303859 | ||||||
chr8:22304669
|
A | G | 6 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1371-115A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 11/22 | chr8 | 22304669 | ||||||
chr8:22304758
|
T | G | 3 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0013g0240 | 3 | HG01175.hp1 HG02027.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1371-26T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 11/22 | chr8 | 22304758 | ||||||
chr8:22304978
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1455+110A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22304978 | ||||||
chr8:22304999
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1455+131T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22304999 | ||||||
chr8:22305082
|
T | G | 1 | a0001c0001t0003g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1455+214T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305082 | ||||||
chr8:22305145
|
G | A | 1 | a0001c0001t0006g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1455+277G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305145 | ||||||
chr8:22305168
|
T | TATTC | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455+304_1455+307d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305168 | |||||
chr8:22305172
|
C | CATTT | 40 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0109others(37): Show | 40 | HG00423.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1455+341_1455+344d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | |||||
chr8:22305172
|
C | CATTTATT others(1): Show |
51 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0157others(48): Show | 51 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1455+337_1455+344d others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | |||||
chr8:22305172
|
C | CATTTATT others(5): Show |
46 | a0001c0001t0003g0004a0001c0001t0003g0239a0001c0001t0003g0255others(43): Show | 46 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1455+333_1455+344d others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | |||||
chr8:22305172
|
C | CATTTATT others(9): Show |
11 | a0001c0001t0003g0237a0001c0001t0003g0271a0001c0001t0004g0181others(8): Show | 11 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1455+329_1455+344d others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | |||||
chr8:22305172
|
CATTT | C | 73 | a0001c0001t0001g0105a0001c0001t0001g0142a0001c0001t0001g0145others(70): Show | 73 | HG00423.hp2 HG00597.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.1455+341_1455+344d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305172 | |||||
chr8:22305176
|
T | C | 2 | a0001c0001t0001g0127a0006c0012t0023g0247 | 2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1455+308T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305176 | ||||||
chr8:22305353
|
C | T | 2 | a0001c0001t0002g0053a0001c0001t0002g0058 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1455+485C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305353 | ||||||
chr8:22305382
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1455+514C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305382 | ||||||
chr8:22305438
|
C | T | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1456-489C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305438 | ||||||
chr8:22305589
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1456-338G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305589 | ||||||
chr8:22305599
|
G | A | 132 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(129): Show | 132 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1456-328G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305599 | ||||||
chr8:22305662
|
AT | A | 16 | a0001c0001t0003g0256a0001c0001t0005g0006a0001c0001t0005g0007others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1456-254delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr8 | 22305662 | |||||
chr8:22305689
|
C | T | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1456-238C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305689 | ||||||
chr8:22305763
|
A | G | 6 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456-164A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305763 | ||||||
chr8:22305818
|
C | T | 147 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(144): Show | 147 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1456-109C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305818 | ||||||
chr8:22305911
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1456-16C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 12/22 | chr8 | 22305911 | ||||||
chr8:22306072
|
T | A | 1 | a0001c0001t0025g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1545+56T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306072 | ||||||
chr8:22306106
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1545+90A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306106 | ||||||
chr8:22306258
|
G | C | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1545+242G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306258 | ||||||
chr8:22306284
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(173): Show | 177 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.1545+268A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306284 | ||||||
chr8:22306463
|
T | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1545+447T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306463 | ||||||
chr8:22306538
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1545+522G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306538 | ||||||
chr8:22306596
|
T | A | 4 | a0001c0001t0004g0226a0001c0001t0004g0227a0010c0008t0004g0231others(1): Show | 4 | HG01069.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545+580T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306596 | ||||||
chr8:22306622
|
C | T | 1 | a0001c0001t0004g0228 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1545+606C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306622 | ||||||
chr8:22306688
|
G | A | 148 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(145): Show | 148 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.1545+672G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306688 | ||||||
chr8:22306776
|
C | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1545+760C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22306776 | ||||||
chr8:22307070
|
A | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0124others(15): Show | 18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1546-863A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307070 | ||||||
chr8:22307118
|
G | A | 147 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(144): Show | 147 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1546-815G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307118 | ||||||
chr8:22307276
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1546-657C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307276 | ||||||
chr8:22307373
|
C | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1546-560C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307373 | ||||||
chr8:22307415
|
T | G | 1 | a0001c0001t0002g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1546-518T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307415 | ||||||
chr8:22307473
|
A | AT | 7 | a0001c0001t0002g0050a0001c0001t0002g0055a0001c0001t0002g0064others(4): Show | 7 | HG01123.hp2 HG02293.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-434dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | |||||
chr8:22307473
|
AT | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(12): Show | 15 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1546-434delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | |||||
chr8:22307473
|
ATT | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0088others(38): Show | 42 | HG00738.hp2 HG01884.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1546-435_1546-434d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | |||||
chr8:22307473
|
ATTT | A | 28 | a0001c0001t0001g0087a0001c0001t0001g0105a0001c0001t0001g0106others(25): Show | 28 | HG00597.hp1 HG01099.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1546-436_1546-434d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | |||||
chr8:22307473
|
ATTTT | A | 11 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(8): Show | 11 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1546-437_1546-434d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | |||||
chr8:22307473
|
ATTTTTT | A | 120 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(117): Show | 120 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1546-439_1546-434d others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | 22307473 | |||||
chr8:22307474
|
T | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1546-459T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307474 | ||||||
chr8:22307475
|
T | A | 7 | a0001c0001t0014g0164a0001c0001t0014g0185a0001c0001t0014g0186others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546-458T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307475 | ||||||
chr8:22307476
|
T | A | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1546-457T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307476 | ||||||
chr8:22307477
|
T | A | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-456T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307477 | ||||||
chr8:22307478
|
T | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1546-455T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307478 | ||||||
chr8:22307479
|
T | A | 3 | a0001c0001t0001g0157a0001c0001t0004g0003a0001c0001t0004g0194 | 3 | HG00609.hp2 NA19001.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1546-454T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307479 | ||||||
chr8:22307480
|
T | A | 120 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(117): Show | 120 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1546-453T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307480 | ||||||
chr8:22307481
|
T | A | 1 | a0001c0001t0004g0219 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1546-452T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307481 | ||||||
chr8:22307530
|
T | C | 133 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(130): Show | 133 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.1546-403T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307530 | ||||||
chr8:22307828
|
C | G | 3 | a0001c0001t0003g0263a0001c0001t0003g0286a0001c0001t0003g0293 | 3 | NA18984.hp2 NA19060.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1546-105C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307828 | ||||||
chr8:22307878
|
A | G | 1 | a0001c0001t0010g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1546-55A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307878 | ||||||
chr8:22307925
|
C | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.1546-8C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 13/22 | chr8 | 22307925 | ||||||
chr8:22308082
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1686+9A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308082 | ||||||
chr8:22308197
|
G | GT | 16 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0090others(13): Show | 16 | HG00639.hp2 HG00741.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1686+140dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | 22308197 | |||||
chr8:22308215
|
A | T | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1686+142A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308215 | ||||||
chr8:22308327
|
A | T | 24 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0127others(21): Show | 24 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1686+254A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308327 | ||||||
chr8:22308464
|
C | G | 1 | a0001c0001t0002g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1686+391C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308464 | ||||||
chr8:22308588
|
G | A | 24 | a0001c0001t0001g0105a0001c0001t0001g0124a0001c0001t0001g0127others(21): Show | 24 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1686+515G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308588 | ||||||
chr8:22308796
|
A | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0136 | 3 | HG02896.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1686+723A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308796 | ||||||
chr8:22308837
|
C | T | 2 | a0001c0001t0010g0230a0001c0001t0010g0232 | 2 | NA18989.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1686+764C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308837 | ||||||
chr8:22308923
|
G | T | 145 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(142): Show | 145 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.1686+850G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308923 | ||||||
chr8:22308942
|
C | T | 6 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1686+869C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22308942 | ||||||
chr8:22309123
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1687-838G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309123 | ||||||
chr8:22309174
|
C | A | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687-787C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309174 | ||||||
chr8:22309568
|
A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1687-393A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309568 | ||||||
chr8:22309633
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1687-328C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309633 | ||||||
chr8:22309634
|
C | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1687-327C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309634 | ||||||
chr8:22309758
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1687-203A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309758 | ||||||
chr8:22309773
|
A | G | 71 | a0001c0001t0001g0157a0001c0001t0002g0045a0001c0001t0003g0195others(68): Show | 71 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1687-188A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309773 | ||||||
chr8:22309873
|
G | T | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1687-88G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 14/22 | chr8 | 22309873 | ||||||
chr8:22310100
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(61): Show | 65 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1800+26A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310100 | ||||||
chr8:22310105
|
A | G | 2 | a0001c0001t0014g0185a0001c0001t0014g0186 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1800+31A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310105 | ||||||
chr8:22310154
|
T | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1800+80T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310154 | ||||||
chr8:22310308
|
A | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0097 | 2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1800+234A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310308 | ||||||
chr8:22310627
|
TAATTA | T | 45 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0170others(42): Show | 45 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1801-481_1801-477d others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr8 | 22310627 | |||||
chr8:22310636
|
A | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0112others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-476A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310636 | ||||||
chr8:22310637
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0112others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-475G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310637 | ||||||
chr8:22310638
|
A | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0112others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-474A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310638 | ||||||
chr8:22310666
|
A | G | 1 | a0003c0002t0012g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1801-446A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310666 | ||||||
chr8:22310833
|
C | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1801-279C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310833 | ||||||
chr8:22310943
|
C | G | 1 | a0011c0009t0004g0207 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1801-169C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310943 | ||||||
chr8:22310962
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1801-150T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 15/22 | chr8 | 22310962 | ||||||
chr8:22311379
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1989+79A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311379 | ||||||
chr8:22311407
|
A | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1989+107A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311407 | ||||||
chr8:22311424
|
G | A | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1989+124G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311424 | ||||||
chr8:22311529
|
G | A | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989+229G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311529 | ||||||
chr8:22311574
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(186): Show | 190 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.1989+274A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311574 | ||||||
chr8:22311609
|
G | A | 4 | a0001c0001t0007g0159a0001c0001t0007g0160a0001c0001t0007g0161others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1989+309G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311609 | ||||||
chr8:22311739
|
A | T | 1 | a0001c0001t0004g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1989+439A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311739 | ||||||
chr8:22311751
|
G | T | 1 | a0001c0001t0001g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1989+451G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311751 | ||||||
chr8:22311765
|
AACTT | A | 4 | a0001c0001t0007g0159a0001c0001t0007g0160a0001c0001t0007g0161others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1989+467_1989+470d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr8 | 22311765 | |||||
chr8:22311813
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(217): Show | 221 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(218): Show |
intron_variant | MODIFIER | c.1989+513C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311813 | ||||||
chr8:22311836
|
A | G | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989+536A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311836 | ||||||
chr8:22311943
|
A | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1989+643A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22311943 | ||||||
chr8:22312022
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1989+722G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312022 | ||||||
chr8:22312265
|
CA | C | 146 | a0001c0001t0001g0087a0001c0001t0001g0157a0001c0001t0001g0287others(143): Show | 146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.1989+982delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr8 | 22312265 | |||||
chr8:22312285
|
A | T | 126 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(123): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1989+985A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312285 | ||||||
chr8:22312347
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1989+1047C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312347 | ||||||
chr8:22312434
|
A | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1989+1134A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312434 | ||||||
chr8:22312566
|
G | A | 130 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(127): Show | 130 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.1989+1266G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22312566 | ||||||
chr8:22313079
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1990-1249A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313079 | ||||||
chr8:22313091
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1990-1237C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313091 | ||||||
chr8:22313163
|
C | T | 7 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0152others(4): Show | 7 | NA18977.hp2 NA18985.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.1990-1165C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313163 | ||||||
chr8:22313323
|
C | A | 4 | a0001c0001t0007g0159a0001c0001t0007g0160a0001c0001t0007g0161others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1990-1005C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313323 | ||||||
chr8:22313353
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1990-975C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313353 | ||||||
chr8:22313462
|
T | C | 1 | a0001c0001t0014g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1990-866T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313462 | ||||||
chr8:22313668
|
G | A | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1990-660G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313668 | ||||||
chr8:22313939
|
A | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(13): Show | 17 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1990-389A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22313939 | ||||||
chr8:22314044
|
G | A | 1 | a0001c0001t0004g0003 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1990-284G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22314044 | ||||||
chr8:22314254
|
A | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1990-74A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 16/22 | chr8 | 22314254 | ||||||
chr8:22314437
|
G | GGT | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091+11_2091+12dup others(2): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr8 | 22314437 | |||||
chr8:22314454
|
C | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2091+25C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | chr8 | 22314454 | ||||||
chr8:22314831
|
A | ATG | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2092-182_2092-181d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr8 | 22314831 | |||||
chr8:22314894
|
AATT | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 10 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2092-130_2092-128d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr8 | 22314894 | |||||
chr8:22315189
|
C | T | 59 | a0001c0001t0002g0045a0001c0001t0004g0003a0001c0001t0004g0181others(56): Show | 59 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.2208+44C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315189 | ||||||
chr8:22315257
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0007g0159a0001c0001t0007g0160others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208+112A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315257 | ||||||
chr8:22315452
|
G | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2208+307G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315452 | ||||||
chr8:22315491
|
AT | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(31): Show | 35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2208+351delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | 22315491 | |||||
chr8:22315498
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(31): Show | 35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2208+353G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315498 | ||||||
chr8:22315533
|
T | C | 1 | a0003c0002t0022g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2208+388T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315533 | ||||||
chr8:22315566
|
C | A | 125 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(122): Show | 125 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.2208+421C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315566 | ||||||
chr8:22315666
|
C | T | 1 | a0001c0001t0003g0196 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2208+521C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315666 | ||||||
chr8:22315885
|
A | T | 2 | a0001c0001t0001g0183a0002c0003t0003g0248 | 2 | HG00597.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2209-360A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315885 | ||||||
chr8:22315906
|
A | G | 1 | a0001c0001t0003g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2209-339A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315906 | ||||||
chr8:22315938
|
A | G | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2209-307A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315938 | ||||||
chr8:22315943
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2209-302G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 18/22 | chr8 | 22315943 | ||||||
chr8:22316462
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2297+129A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22316462 | ||||||
chr8:22316787
|
A | G | 1 | a0001c0001t0018g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2297+454A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22316787 | ||||||
chr8:22316869
|
C | G | 1 | a0001c0001t0011g0034 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2297+536C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22316869 | ||||||
chr8:22317013
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(258): Show | 262 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.2297+680T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317013 | ||||||
chr8:22317106
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2297+773G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317106 | ||||||
chr8:22317119
|
C | T | 4 | a0001c0001t0007g0159a0001c0001t0007g0160a0001c0001t0007g0161others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2297+786C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317119 | ||||||
chr8:22317210
|
T | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2297+877T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317210 | ||||||
chr8:22317248
|
A | G | 1 | a0001c0001t0004g0003 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2297+915A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317248 | ||||||
chr8:22317269
|
G | C | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2298-901G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317269 | ||||||
chr8:22317355
|
C | A | 3 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0141 | 3 | NA18969.hp1 NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2298-815C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317355 | ||||||
chr8:22317391
|
A | AAC | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2298-765_2298-764d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 22317391 | |||||
chr8:22317507
|
C | T | 1 | a0001c0001t0013g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2298-663C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317507 | ||||||
chr8:22317573
|
A | G | 27 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(24): Show | 27 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2298-597A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317573 | ||||||
chr8:22317599
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2298-571A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317599 | ||||||
chr8:22317649
|
T | A | 6 | a0001c0001t0003g0263a0003c0002t0001g0019a0003c0002t0012g0016others(3): Show | 6 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2298-521T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317649 | ||||||
chr8:22317669
|
A | T | 14 | a0001c0001t0001g0027a0001c0001t0001g0089a0001c0001t0001g0105others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2298-501A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317669 | ||||||
chr8:22317669
|
AT | A | 19 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.2298-493delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | 22317669 | |||||
chr8:22317673
|
T | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | HG00733.hp1 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2298-497T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317673 | ||||||
chr8:22317855
|
G | T | 126 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(123): Show | 126 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.2298-315G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317855 | ||||||
chr8:22317950
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0169 | 2 | HG02280.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2298-220C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22317950 | ||||||
chr8:22318020
|
G | A | 162 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(159): Show | 162 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.2298-150G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22318020 | ||||||
chr8:22318054
|
C | T | 146 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(143): Show | 146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2298-116C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22318054 | ||||||
chr8:22318071
|
T | C | 1 | a0001c0001t0003g0279 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2298-99T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 19/22 | chr8 | 22318071 | ||||||
chr8:22318357
|
G | A | 1 | a0001c0001t0014g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2403+82G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318357 | ||||||
chr8:22318474
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2403+199C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318474 | ||||||
chr8:22318507
|
G | T | 1 | a0001c0001t0015g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2403+232G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318507 | ||||||
chr8:22318593
|
C | T | 1 | a0001c0001t0004g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2403+318C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318593 | ||||||
chr8:22318607
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0118 | 3 | HG00738.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2403+332C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318607 | ||||||
chr8:22318657
|
T | C | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+382T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318657 | ||||||
chr8:22318878
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2403+603T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318878 | ||||||
chr8:22318897
|
A | T | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2403+622A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318897 | ||||||
chr8:22318955
|
T | A | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2403+680T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22318955 | ||||||
chr8:22319190
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2403+915G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319190 | ||||||
chr8:22319204
|
T | C | 7 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+929T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319204 | ||||||
chr8:22319255
|
C | T | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+980C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319255 | ||||||
chr8:22319337
|
A | G | 4 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0260others(1): Show | 4 | HG00735.hp2 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2403+1062A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319337 | ||||||
chr8:22319683
|
C | A | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+1408C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319683 | ||||||
chr8:22319731
|
A | T | 71 | a0001c0001t0001g0157a0001c0001t0002g0045a0001c0001t0003g0195others(68): Show | 71 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2403+1456A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319731 | ||||||
chr8:22319816
|
G | C | 6 | a0001c0001t0001g0127a0001c0001t0007g0159a0001c0001t0007g0160others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+1541G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319816 | ||||||
chr8:22319860
|
C | G | 2 | a0001c0001t0002g0099a0001c0001t0002g0100 | 2 | HG00408.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2403+1585C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319860 | ||||||
chr8:22319896
|
G | C | 1 | a0001c0001t0004g0251 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2403+1621G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319896 | ||||||
chr8:22319956
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2403+1681T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22319956 | ||||||
chr8:22320163
|
G | A | 3 | a0001c0001t0002g0090a0001c0001t0002g0094a0001c0001t0002g0095 | 3 | HG02818.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2403+1888G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320163 | ||||||
chr8:22320259
|
C | CT | 29 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0143others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.2403+2006dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22320259 | |||||
chr8:22320259
|
C | CTT | 63 | a0001c0001t0001g0157a0001c0001t0002g0045a0001c0001t0003g0195others(60): Show | 63 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2403+2005_2403+200 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22320259 | |||||
chr8:22320259
|
C | CTTT | 7 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0211others(4): Show | 7 | HG01109.hp1 HG01261.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+2004_2403+200 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22320259 | |||||
chr8:22320399
|
C | T | 57 | a0001c0001t0004g0003a0001c0001t0004g0181a0001c0001t0004g0182others(54): Show | 57 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.2403+2124C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320399 | ||||||
chr8:22320471
|
C | T | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+2196C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320471 | ||||||
chr8:22320534
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2403+2259C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320534 | ||||||
chr8:22320739
|
C | T | 1 | a0001c0001t0006g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2403+2464C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320739 | ||||||
chr8:22320839
|
C | A | 1 | a0001c0001t0015g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2403+2564C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320839 | ||||||
chr8:22320936
|
GACTGTCT others(6): Show |
G | 1 | a0001c0001t0002g0080 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2403+2662_2403+267 others(17): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320936 | ||||||
chr8:22320996
|
G | A | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+2721G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22320996 | ||||||
chr8:22321043
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+2768G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321043 | ||||||
chr8:22321229
|
T | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(220): Show | 224 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(221): Show |
intron_variant | MODIFIER | c.2403+2954T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321229 | ||||||
chr8:22321269
|
C | A | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+2994C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321269 | ||||||
chr8:22321674
|
T | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+3399T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321674 | ||||||
chr8:22321823
|
T | A | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2403+3548T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321823 | ||||||
chr8:22321823
|
T | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(286): Show | 290 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.2403+3548T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321823 | ||||||
chr8:22321894
|
C | A | 1 | a0001c0001t0004g0243 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2403+3619C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22321894 | ||||||
chr8:22322250
|
C | T | 24 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(21): Show | 24 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2403+3975C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322250 | ||||||
chr8:22322256
|
C | G | 1 | a0001c0001t0015g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2403+3981C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322256 | ||||||
chr8:22322331
|
G | C | 128 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0045others(125): Show | 128 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2403+4056G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322331 | ||||||
chr8:22322445
|
G | T | 1 | a0001c0001t0004g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2403+4170G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322445 | ||||||
chr8:22322536
|
G | A | 2 | a0001c0001t0001g0183a0006c0012t0023g0247 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2403+4261G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322536 | ||||||
chr8:22322580
|
TGTCCCGT others(3): Show |
T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+4310_2403+431 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22322580 | |||||
chr8:22322691
|
C | T | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+4416C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322691 | ||||||
chr8:22322729
|
C | T | 16 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2403+4454C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322729 | ||||||
chr8:22322821
|
G | A | 131 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(128): Show | 131 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.2403+4546G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322821 | ||||||
chr8:22322834
|
C | T | 11 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(8): Show | 11 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.2403+4559C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322834 | ||||||
chr8:22322892
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2403+4617A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22322892 | ||||||
chr8:22323114
|
G | A | 146 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(143): Show | 146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2403+4839G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323114 | ||||||
chr8:22323114
|
G | C | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2403+4839G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323114 | ||||||
chr8:22323114
|
G | T | 1 | a0001c0001t0015g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2403+4839G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323114 | ||||||
chr8:22323143
|
C | CT | 41 | a0001c0001t0001g0027a0001c0001t0001g0119a0001c0001t0001g0120others(38): Show | 41 | HG00597.hp2 HG01070.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.2403+4890dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22323143 | |||||
chr8:22323143
|
C | CTT | 130 | a0001c0001t0001g0122a0001c0001t0001g0135a0001c0001t0001g0145others(127): Show | 130 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.2403+4889_2403+489 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22323143 | |||||
chr8:22323143
|
C | CTTT | 31 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0110others(28): Show | 31 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.2403+4888_2403+489 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22323143 | |||||
chr8:22323211
|
A | G | 147 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(144): Show | 147 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2403+4936A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323211 | ||||||
chr8:22323216
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2403+4941C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323216 | ||||||
chr8:22323238
|
C | G | 1 | a0001c0001t0004g0190 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2403+4963C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323238 | ||||||
chr8:22323272
|
C | T | 23 | a0001c0001t0001g0027a0001c0001t0001g0119a0001c0001t0001g0120others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.2403+4997C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323272 | ||||||
chr8:22323315
|
T | C | 20 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(17): Show | 20 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2403+5040T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323315 | ||||||
chr8:22323327
|
T | C | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+5052T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323327 | ||||||
chr8:22323388
|
C | T | 1 | a0001c0001t0006g0295 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2403+5113C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323388 | ||||||
chr8:22323543
|
T | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+5268T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323543 | ||||||
chr8:22323642
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2403+5367T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323642 | ||||||
chr8:22323815
|
A | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0097 | 2 | NA18950.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.2403+5540A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323815 | ||||||
chr8:22323850
|
T | G | 173 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(170): Show | 173 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.2403+5575T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22323850 | ||||||
chr8:22324079
|
T | A | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+5804T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324079 | ||||||
chr8:22324139
|
G | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0150others(3): Show | 6 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+5864G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324139 | ||||||
chr8:22324214
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2403+5939A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324214 | ||||||
chr8:22324259
|
C | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00597.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2403+5984C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324259 | ||||||
chr8:22324263
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2403+5988A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324263 | ||||||
chr8:22324369
|
T | C | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2403+6094T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324369 | ||||||
chr8:22324635
|
A | C | 1 | a0001c0001t0002g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2403+6360A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324635 | ||||||
chr8:22324703
|
T | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+6428T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324703 | ||||||
chr8:22324806
|
AC | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(32): Show | 36 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(33): Show |
intron_variant | MODIFIER | c.2403+6532delC | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324806 | ||||||
chr8:22324908
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2403+6633G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22324908 | ||||||
chr8:22325072
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+6797G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325072 | ||||||
chr8:22325171
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2403+6896C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325171 | ||||||
chr8:22325181
|
A | G | 2 | a0001c0001t0014g0185a0001c0001t0014g0186 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2403+6906A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325181 | ||||||
chr8:22325481
|
C | CT | 86 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(83): Show | 86 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.2403+7228dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | |||||
chr8:22325481
|
C | CTT | 76 | a0001c0001t0001g0151a0001c0001t0001g0157a0001c0001t0001g0167others(73): Show | 76 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2403+7227_2403+722 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | |||||
chr8:22325481
|
CT | C | 28 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0112others(25): Show | 28 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.2403+7228delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | |||||
chr8:22325481
|
CTTTTT | C | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+7224_2403+722 others(9): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22325481 | |||||
chr8:22325695
|
C | T | 5 | a0001c0001t0004g0203a0001c0001t0004g0204a0001c0001t0004g0205others(2): Show | 5 | HG01358.hp1 HG01978.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+7420C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325695 | ||||||
chr8:22325759
|
C | T | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2403+7484C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325759 | ||||||
chr8:22325877
|
G | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0029 | 2 | NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2403+7602G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325877 | ||||||
chr8:22325927
|
C | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+7652C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325927 | ||||||
chr8:22325963
|
T | C | 1 | a0001c0001t0004g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2403+7688T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22325963 | ||||||
chr8:22326031
|
A | G | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+7756A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326031 | ||||||
chr8:22326053
|
C | G | 2 | a0001c0001t0002g0028a0001c0001t0002g0029 | 2 | NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2403+7778C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326053 | ||||||
chr8:22326123
|
A | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0167others(3): Show | 6 | HG00733.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+7848A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326123 | ||||||
chr8:22326211
|
TA | T | 16 | a0001c0001t0002g0141a0001c0001t0005g0006a0001c0001t0005g0007others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2403+7950delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22326211 | |||||
chr8:22326304
|
T | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG01109.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2403+8029T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326304 | ||||||
chr8:22326409
|
G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(11): Show | 15 | HG00738.hp2 HG02004.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2403+8134G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326409 | ||||||
chr8:22326463
|
G | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(291): Show | 295 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.2403+8188G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326463 | ||||||
chr8:22326535
|
A | G | 2 | a0001c0001t0001g0105a0006c0012t0023g0247 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2403+8260A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326535 | ||||||
chr8:22326659
|
G | A | 1 | a0001c0001t0014g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2403+8384G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326659 | ||||||
chr8:22326661
|
A | G | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+8386A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22326661 | ||||||
chr8:22327024
|
C | CT | 178 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(175): Show | 179 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.2403+8770dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327024 | |||||
chr8:22327024
|
C | CTT | 34 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(31): Show | 34 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.2403+8769_2403+877 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327024 | |||||
chr8:22327024
|
C | CTTT | 12 | a0001c0001t0003g0268a0001c0001t0005g0006a0001c0001t0005g0007others(9): Show | 12 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2403+8768_2403+877 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327024 | |||||
chr8:22327292
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2403+9017C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327292 | ||||||
chr8:22327368
|
C | T | 147 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(144): Show | 147 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2403+9093C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327368 | ||||||
chr8:22327369
|
G | GT | 37 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0144others(34): Show | 37 | HG00597.hp1 HG00733.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2403+9109dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22327369 | |||||
chr8:22327374
|
T | G | 1 | a0001c0001t0004g0003 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2403+9099T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327374 | ||||||
chr8:22327424
|
A | G | 132 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(129): Show | 132 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2403+9149A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327424 | ||||||
chr8:22327429
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+9154G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327429 | ||||||
chr8:22327592
|
C | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2403+9317C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327592 | ||||||
chr8:22327979
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2403+9704T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327979 | ||||||
chr8:22327986
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2403+9711C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22327986 | ||||||
chr8:22328055
|
T | G | 1 | a0003c0002t0022g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2403+9780T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328055 | ||||||
chr8:22328448
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2403+10173G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328448 | ||||||
chr8:22328463
|
G | A | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+10188G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328463 | ||||||
chr8:22328465
|
A | G | 4 | a0001c0001t0004g0226a0001c0001t0004g0227a0010c0008t0004g0231others(1): Show | 4 | HG01069.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+10190A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328465 | ||||||
chr8:22328593
|
T | C | 1 | a0004c0004t0009g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2403+10318T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328593 | ||||||
chr8:22328634
|
T | A | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+10359T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328634 | ||||||
chr8:22328818
|
G | GT | 11 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0130others(8): Show | 11 | HG01516.hp1 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2403+10562dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22328818 | |||||
chr8:22328818
|
G | GTT | 128 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(125): Show | 128 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2403+10561_2403+10 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22328818 | |||||
chr8:22328818
|
G | T | 3 | a0001c0001t0004g0251a0001c0001t0008g0184a0001c0001t0028g0252 | 3 | HG02976.hp2 NA18612.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.2403+10543G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328818 | ||||||
chr8:22328818
|
GT | G | 19 | a0001c0001t0001g0087a0001c0001t0002g0041a0001c0001t0002g0065others(16): Show | 19 | HG00639.hp2 HG01069.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.2403+10562delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22328818 | |||||
chr8:22328820
|
T | C | 1 | a0001c0001t0015g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2403+10545T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328820 | ||||||
chr8:22328825
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2403+10550T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328825 | ||||||
chr8:22328916
|
T | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG01109.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2403+10641T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22328916 | ||||||
chr8:22329022
|
C | G | 1 | a0001c0001t0002g0078 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2403+10747C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329022 | ||||||
chr8:22329095
|
C | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(227): Show | 231 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.2403+10820C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329095 | ||||||
chr8:22329105
|
C | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(227): Show | 231 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.2403+10830C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329105 | ||||||
chr8:22329391
|
G | A | 1 | a0001c0001t0004g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2403+11116G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329391 | ||||||
chr8:22329502
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(270): Show | 274 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.2403+11227C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329502 | ||||||
chr8:22329539
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2403+11264T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329539 | ||||||
chr8:22329574
|
C | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+11299C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329574 | ||||||
chr8:22329620
|
A | G | 2 | a0001c0001t0004g0220a0001c0001t0004g0221 | 2 | HG01361.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2403+11345A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329620 | ||||||
chr8:22329915
|
A | T | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2403+11640A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329915 | ||||||
chr8:22329985
|
C | G | 136 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(133): Show | 136 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2403+11710C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22329985 | ||||||
chr8:22330261
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2403+11986A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330261 | ||||||
chr8:22330342
|
A | G | 134 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(131): Show | 134 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2403+12067A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330342 | ||||||
chr8:22330421
|
G | A | 1 | a0001c0001t0003g0263 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2403+12146G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330421 | ||||||
chr8:22330546
|
C | A | 157 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(154): Show | 157 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2403+12271C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330546 | ||||||
chr8:22330557
|
C | G | 1 | a0001c0001t0002g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2403+12282C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330557 | ||||||
chr8:22330697
|
A | AAAAT | 71 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2403+12466_2403+12 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330697
|
A | AAAATAAA others(1): Show |
26 | a0001c0001t0001g0154a0001c0001t0002g0032a0001c0001t0002g0045others(23): Show | 26 | HG00738.hp1 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2403+12462_2403+12 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330697
|
A | AAAATAAA others(5): Show |
6 | a0001c0001t0002g0035a0001c0001t0003g0195a0001c0001t0003g0196others(3): Show | 6 | HG00609.hp1 HG01517.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403+12458_2403+12 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330697
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0003g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2403+12454_2403+12 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330697
|
AAAAT | A | 56 | a0001c0001t0001g0168a0001c0001t0002g0025a0001c0001t0002g0026others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2403+12466_2403+12 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330697
|
AAAATAAA others(1): Show |
A | 5 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+12462_2403+12 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330697
|
AAAATAAA others(5): Show |
A | 6 | a0001c0001t0001g0124a0001c0001t0001g0132a0001c0001t0001g0144others(3): Show | 6 | HG03516.hp1 NA18906.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403+12458_2403+12 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330697
|
AAAATAAA others(9): Show |
A | 47 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(44): Show | 48 | HG00597.hp1 HG00738.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2403+12454_2403+12 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330697 | |||||
chr8:22330741
|
T | TAAATAAA others(1): Show |
3 | a0001c0001t0004g0254a0001c0001t0006g0040a0001c0001t0006g0295 | 3 | HG02602.hp1 HG04228.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2403+12469_2403+12 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22330741 | |||||
chr8:22330745
|
A | T | 5 | a0001c0001t0001g0157a0001c0001t0003g0259a0001c0001t0004g0204others(2): Show | 5 | HG01358.hp1 HG01358.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+12470A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330745 | ||||||
chr8:22330817
|
T | C | 141 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(138): Show | 141 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.2403+12542T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330817 | ||||||
chr8:22330865
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2403+12590A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330865 | ||||||
chr8:22330932
|
T | C | 1 | a0001c0001t0003g0258 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2403+12657T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330932 | ||||||
chr8:22330945
|
C | T | 1 | a0003c0002t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2403+12670C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330945 | ||||||
chr8:22330983
|
T | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+12708T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22330983 | ||||||
chr8:22331004
|
G | A | 1 | a0001c0001t0004g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2403+12729G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331004 | ||||||
chr8:22331107
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2403+12832T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331107 | ||||||
chr8:22331130
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2403+12855T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331130 | ||||||
chr8:22331303
|
C | G | 1 | a0001c0001t0004g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2403+13028C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331303 | ||||||
chr8:22331447
|
A | G | 1 | a0001c0001t0004g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2403+13172A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331447 | ||||||
chr8:22331483
|
T | C | 1 | a0001c0001t0004g0214 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2403+13208T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331483 | ||||||
chr8:22331797
|
T | C | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2403+13522T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331797 | ||||||
chr8:22331862
|
A | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0058 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2403+13587A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22331862 | ||||||
chr8:22332217
|
A | G | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2403+13942A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332217 | ||||||
chr8:22332472
|
C | G | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+14197C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332472 | ||||||
chr8:22332617
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0140 | 2 | HG01517.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2403+14342A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332617 | ||||||
chr8:22332726
|
A | G | 3 | a0001c0001t0014g0164a0001c0001t0014g0185a0001c0001t0014g0186 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2403+14451A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332726 | ||||||
chr8:22332887
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2403+14612G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332887 | ||||||
chr8:22332967
|
G | A | 1 | a0001c0001t0018g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2403+14692G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22332967 | ||||||
chr8:22333113
|
T | C | 1 | a0001c0001t0014g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2403+14838T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333113 | ||||||
chr8:22333139
|
T | C | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+14864T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333139 | ||||||
chr8:22333314
|
G | A | 16 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2403+15039G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333314 | ||||||
chr8:22333540
|
A | G | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+15265A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333540 | ||||||
chr8:22333600
|
G | A | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403+15325G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333600 | ||||||
chr8:22333648
|
T | C | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2403+15373T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333648 | ||||||
chr8:22333990
|
G | C | 132 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0031others(129): Show | 132 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2403+15715G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22333990 | ||||||
chr8:22334057
|
T | A | 1 | a0001c0001t0002g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2403+15782T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334057 | ||||||
chr8:22334059
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2403+15784C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334059 | ||||||
chr8:22334323
|
A | G | 157 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(154): Show | 157 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2403+16048A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334323 | ||||||
chr8:22334335
|
C | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+16060C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334335 | ||||||
chr8:22334437
|
G | A | 2 | a0001c0001t0002g0099a0001c0001t0002g0100 | 2 | HG00408.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2403+16162G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334437 | ||||||
chr8:22334519
|
C | CA | 141 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(138): Show | 141 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.2403+16257dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22334519 | |||||
chr8:22334519
|
CA | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+16257delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22334519 | |||||
chr8:22334668
|
A | G | 1 | a0001c0001t0018g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2403+16393A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334668 | ||||||
chr8:22334865
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2403+16590G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22334865 | ||||||
chr8:22335072
|
A | AT | 140 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(137): Show | 140 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.2403+16797_2403+16 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335072 | ||||||
chr8:22335072
|
A | T | 13 | a0001c0001t0002g0140a0001c0001t0004g0203a0001c0001t0004g0253others(10): Show | 13 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.2403+16797A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335072 | ||||||
chr8:22335101
|
A | G | 23 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(20): Show | 23 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2403+16826A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335101 | ||||||
chr8:22335163
|
A | G | 1 | a0001c0001t0005g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2403+16888A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335163 | ||||||
chr8:22335179
|
A | G | 158 | a0001c0001t0001g0157a0001c0001t0001g0287a0001c0001t0001g0288others(155): Show | 158 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.2403+16904A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335179 | ||||||
chr8:22335189
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2403+16914A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335189 | ||||||
chr8:22335259
|
C | T | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2403+16984C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335259 | ||||||
chr8:22335292
|
C | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2403+17017C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335292 | ||||||
chr8:22335325
|
T | G | 21 | a0001c0001t0001g0027a0001c0001t0001g0119a0001c0001t0001g0120others(18): Show | 21 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2403+17050T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335325 | ||||||
chr8:22335334
|
A | G | 24 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(21): Show | 24 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2403+17059A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335334 | ||||||
chr8:22335419
|
T | C | 1 | a0001c0001t0003g0195 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2403+17144T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335419 | ||||||
chr8:22335427
|
TCATA | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(287): Show | 291 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.2403+17157_2403+17 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335427 | |||||
chr8:22335543
|
C | CT | 13 | a0001c0001t0001g0120a0001c0001t0001g0143a0001c0001t0001g0152others(10): Show | 13 | HG01074.hp1 HG01175.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2403+17290dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335543 | |||||
chr8:22335543
|
CT | C | 146 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0111others(143): Show | 146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2403+17290delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335543 | |||||
chr8:22335543
|
CTT | C | 10 | a0001c0001t0001g0110a0001c0001t0001g0287a0001c0001t0003g0289others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2403+17289_2403+17 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22335543 | |||||
chr8:22335567
|
A | G | 1 | a0001c0001t0004g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2403+17292A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335567 | ||||||
chr8:22335575
|
T | C | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2403+17300T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335575 | ||||||
chr8:22335643
|
G | C | 5 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(2): Show | 5 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-17316G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335643 | ||||||
chr8:22335672
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2404-17287C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335672 | ||||||
chr8:22335802
|
A | G | 13 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0001g0154others(10): Show | 13 | HG00733.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2404-17157A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335802 | ||||||
chr8:22335839
|
G | A | 1 | a0001c0001t0029g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2404-17120G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335839 | ||||||
chr8:22335848
|
T | C | 1 | a0001c0001t0003g0262 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2404-17111T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22335848 | ||||||
chr8:22336012
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2404-16947A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336012 | ||||||
chr8:22336187
|
C | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-16772C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336187 | ||||||
chr8:22336210
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2404-16749G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336210 | ||||||
chr8:22336255
|
T | C | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-16704T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336255 | ||||||
chr8:22336424
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-16535G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336424 | ||||||
chr8:22336510
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2404-16449G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336510 | ||||||
chr8:22336568
|
A | G | 2 | a0001c0001t0003g0004a0001c0001t0027g0005 | 2 | NA19009.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2404-16391A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336568 | ||||||
chr8:22336703
|
C | T | 1 | a0001c0001t0003g0271 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2404-16256C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336703 | ||||||
chr8:22336974
|
A | G | 1 | a0001c0001t0004g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2404-15985A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22336974 | ||||||
chr8:22337070
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2404-15889C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337070 | ||||||
chr8:22337324
|
A | G | 2 | a0001c0001t0014g0164a0001c0001t0014g0186 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2404-15635A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337324 | ||||||
chr8:22337341
|
A | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2404-15618A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337341 | ||||||
chr8:22337355
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-15604G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337355 | ||||||
chr8:22337486
|
T | C | 4 | a0001c0001t0003g0266a0001c0001t0003g0269a0001c0001t0003g0270others(1): Show | 4 | NA18940.hp1 NA18964.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-15473T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337486 | ||||||
chr8:22337510
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2404-15449C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337510 | ||||||
chr8:22337570
|
TA | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-15377delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22337570 | |||||
chr8:22337943
|
T | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-15016T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22337943 | ||||||
chr8:22338092
|
C | CA | 6 | a0001c0001t0001g0123a0001c0001t0006g0021a0001c0001t0006g0022others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-14856dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338092 | |||||
chr8:22338168
|
A | G | 1 | a0001c0001t0005g0010 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2404-14791A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338168 | ||||||
chr8:22338172
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(285): Show | 289 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.2404-14787C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338172 | ||||||
chr8:22338225
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-14734G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338225 | ||||||
chr8:22338337
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2404-14622A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338337 | ||||||
chr8:22338445
|
C | G | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-14514C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338445 | ||||||
chr8:22338691
|
A | AAAAT | 23 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0109others(20): Show | 23 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2404-14237_2404-14 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | |||||
chr8:22338691
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2404-14245_2404-14 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | |||||
chr8:22338691
|
AAAAT | A | 130 | a0001c0001t0001g0157a0001c0001t0003g0002a0001c0001t0003g0004others(127): Show | 130 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.2404-14237_2404-14 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | |||||
chr8:22338691
|
AAAATAAA others(1): Show |
A | 11 | a0001c0001t0001g0105a0001c0001t0005g0006a0001c0001t0005g0007others(8): Show | 11 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.2404-14241_2404-14 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22338691 | |||||
chr8:22338811
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0114a0001c0001t0001g0118 | 4 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-14148G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338811 | ||||||
chr8:22338915
|
C | G | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-14044C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338915 | ||||||
chr8:22338970
|
A | G | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-13989A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22338970 | ||||||
chr8:22339034
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-13925A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339034 | ||||||
chr8:22339248
|
C | T | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2404-13711C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339248 | ||||||
chr8:22339331
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2404-13628C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339331 | ||||||
chr8:22339376
|
C | T | 122 | a0001c0001t0001g0157a0001c0001t0003g0002a0001c0001t0003g0004others(119): Show | 122 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.2404-13583C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339376 | ||||||
chr8:22339380
|
C | T | 8 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2404-13579C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339380 | ||||||
chr8:22339393
|
A | G | 1 | a0004c0004t0009g0178 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2404-13566A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339393 | ||||||
chr8:22339416
|
G | C | 4 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02004.hp1 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-13543G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339416 | ||||||
chr8:22339466
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2404-13493C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339466 | ||||||
chr8:22339506
|
C | CA | 66 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(63): Show | 67 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2404-13443dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22339506 | |||||
chr8:22339581
|
C | G | 146 | a0001c0001t0001g0157a0001c0001t0003g0002a0001c0001t0003g0004others(143): Show | 146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2404-13378C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339581 | ||||||
chr8:22339599
|
C | T | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-13360C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339599 | ||||||
chr8:22339600
|
G | A | 3 | a0001c0001t0002g0046a0001c0001t0002g0050a0001c0001t0002g0059 | 3 | HG00733.hp2 HG01123.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2404-13359G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339600 | ||||||
chr8:22339637
|
A | G | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-13322A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339637 | ||||||
chr8:22339721
|
C | T | 4 | a0001c0001t0002g0090a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-13238C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339721 | ||||||
chr8:22339818
|
C | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0125others(15): Show | 18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-13141C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339818 | ||||||
chr8:22339839
|
G | A | 146 | a0001c0001t0001g0157a0001c0001t0003g0002a0001c0001t0003g0004others(143): Show | 146 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2404-13120G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339839 | ||||||
chr8:22339971
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-12988G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22339971 | ||||||
chr8:22340045
|
A | AT | 51 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(48): Show | 52 | HG00423.hp2 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2404-12890dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | |||||
chr8:22340045
|
A | ATT | 14 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0167others(11): Show | 14 | HG00733.hp1 HG00741.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-12891_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | |||||
chr8:22340045
|
A | ATTT | 88 | a0001c0001t0001g0157a0001c0001t0002g0045a0001c0001t0003g0002others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2404-12892_2404-12 others(9): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | |||||
chr8:22340045
|
A | ATTTT | 33 | a0001c0001t0003g0004a0001c0001t0003g0239a0001c0001t0003g0255others(30): Show | 33 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2404-12893_2404-12 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | |||||
chr8:22340045
|
ATT | A | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(11): Show | 14 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-12891_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340045 | |||||
chr8:22340074
|
A | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(291): Show | 295 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(292): Show |
intron_variant | MODIFIER | c.2404-12885A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340074 | ||||||
chr8:22340130
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-12829G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340130 | ||||||
chr8:22340139
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2404-12820G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340139 | ||||||
chr8:22340146
|
G | A | 3 | a0001c0001t0003g0237a0001c0001t0004g0003a0001c0001t0013g0240 | 3 | HG02027.hp2 NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2404-12813G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340146 | ||||||
chr8:22340197
|
CAT | C | 9 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2404-12761_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340197 | ||||||
chr8:22340235
|
T | C | 1 | a0001c0001t0025g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2404-12724T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340235 | ||||||
chr8:22340478
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2404-12481A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340478 | ||||||
chr8:22340501
|
T | TAG | 22 | a0001c0001t0001g0027a0001c0001t0001g0119a0001c0001t0001g0120others(19): Show | 22 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.2404-12455_2404-12 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22340501 | |||||
chr8:22340548
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2404-12411G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340548 | ||||||
chr8:22340623
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2404-12336G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340623 | ||||||
chr8:22340900
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-12059A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22340900 | ||||||
chr8:22341299
|
TA | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-11646delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341299 | |||||
chr8:22341377
|
C | T | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2404-11582C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341377 | ||||||
chr8:22341429
|
C | T | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-11530C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341429 | ||||||
chr8:22341468
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(218): Show | 222 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(219): Show |
intron_variant | MODIFIER | c.2404-11491A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341468 | ||||||
chr8:22341478
|
C | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 9 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-11481C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341478 | ||||||
chr8:22341595
|
C | CA | 139 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0151others(136): Show | 139 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2404-11346dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341595 | |||||
chr8:22341595
|
C | CAA | 6 | a0001c0001t0003g0239a0002c0003t0003g0245a0004c0004t0009g0174others(3): Show | 6 | HG01175.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-11347_2404-11 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341595 | |||||
chr8:22341611
|
A | AG | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0132others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-11348_2404-11 others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341611 | ||||||
chr8:22341754
|
A | G | 1 | a0001c0001t0003g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2404-11205A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341754 | ||||||
chr8:22341757
|
A | G | 2 | a0001c0001t0002g0033a0001c0001t0021g0030 | 2 | HG00735.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2404-11202A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341757 | ||||||
chr8:22341832
|
A | G | 3 | a0001c0001t0014g0164a0001c0001t0014g0185a0001c0001t0014g0186 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2404-11127A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22341832 | ||||||
chr8:22341977
|
T | TA | 25 | a0001c0001t0001g0145a0001c0001t0001g0152a0001c0001t0002g0028others(22): Show | 25 | HG00741.hp1 HG01167.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.2404-10964dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341977 | |||||
chr8:22341977
|
TA | T | 19 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0108others(16): Show | 19 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2404-10964delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341977 | |||||
chr8:22341977
|
TAA | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0106others(7): Show | 11 | HG00738.hp2 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2404-10965_2404-10 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22341977 | |||||
chr8:22342000
|
A | C | 1 | a0001c0001t0004g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2404-10959A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342000 | ||||||
chr8:22342157
|
C | CA | 132 | a0001c0001t0001g0155a0001c0001t0002g0045a0001c0001t0003g0002others(129): Show | 132 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2404-10799dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22342157 | |||||
chr8:22342393
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-10566G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342393 | ||||||
chr8:22342542
|
A | G | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-10417A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342542 | ||||||
chr8:22342546
|
T | C | 3 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01891.hp2 HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2404-10413T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342546 | ||||||
chr8:22342552
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2404-10407T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342552 | ||||||
chr8:22342567
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10392C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342567 | ||||||
chr8:22342568
|
C | A | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10391C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342568 | ||||||
chr8:22342570
|
G | A | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10389G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342570 | ||||||
chr8:22342575
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10384C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342575 | ||||||
chr8:22342576
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10383A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342576 | ||||||
chr8:22342578
|
A | T | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10381A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342578 | ||||||
chr8:22342579
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10380A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342579 | ||||||
chr8:22342580
|
A | T | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10379A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342580 | ||||||
chr8:22342581
|
A | T | 1 | a0001c0001t0002g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2404-10378A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342581 | ||||||
chr8:22342613
|
A | C | 1 | a0001c0001t0004g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2404-10346A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342613 | ||||||
chr8:22342635
|
A | G | 124 | a0001c0001t0001g0155a0001c0001t0002g0045a0001c0001t0003g0002others(121): Show | 124 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.2404-10324A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342635 | ||||||
chr8:22342717
|
G | T | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-10242G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342717 | ||||||
chr8:22342721
|
T | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-10238T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22342721 | ||||||
chr8:22343002
|
C | T | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-9957C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343002 | ||||||
chr8:22343170
|
C | T | 123 | a0001c0001t0001g0155a0001c0001t0002g0045a0001c0001t0003g0002others(120): Show | 123 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.2404-9789C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343170 | ||||||
chr8:22343171
|
G | A | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2404-9788G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343171 | ||||||
chr8:22343233
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(56): Show | 60 | HG00597.hp1 HG00733.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.2404-9726C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343233 | ||||||
chr8:22343261
|
G | A | 1 | a0009c0007t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2404-9698G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343261 | ||||||
chr8:22343313
|
A | G | 2 | a0002c0003t0003g0244a0002c0003t0003g0245 | 2 | NA19056.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2404-9646A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343313 | ||||||
chr8:22343422
|
C | T | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-9537C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343422 | ||||||
chr8:22343435
|
C | CA | 7 | a0001c0001t0002g0078a0001c0001t0008g0184a0003c0002t0001g0019others(4): Show | 7 | HG01099.hp2 HG02074.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-9511dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22343435 | |||||
chr8:22343450
|
T | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-9509T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343450 | ||||||
chr8:22343470
|
T | C | 143 | a0001c0001t0001g0155a0001c0001t0002g0045a0001c0001t0003g0002others(140): Show | 143 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.2404-9489T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343470 | ||||||
chr8:22343487
|
A | G | 3 | a0001c0001t0014g0164a0001c0001t0014g0185a0001c0001t0014g0186 | 3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2404-9472A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343487 | ||||||
chr8:22343609
|
G | A | 6 | a0001c0001t0001g0183a0004c0004t0009g0174a0004c0004t0009g0176others(3): Show | 6 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-9350G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343609 | ||||||
chr8:22343610
|
A | G | 127 | a0001c0001t0001g0155a0001c0001t0002g0045a0001c0001t0003g0002others(124): Show | 127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2404-9349A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343610 | ||||||
chr8:22343770
|
G | A | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2404-9189G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343770 | ||||||
chr8:22343789
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2404-9170G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343789 | ||||||
chr8:22343914
|
C | T | 1 | a0001c0010t0003g0173 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2404-9045C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22343914 | ||||||
chr8:22344191
|
A | G | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-8768A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344191 | ||||||
chr8:22344206
|
T | C | 127 | a0001c0001t0001g0155a0001c0001t0002g0045a0001c0001t0003g0002others(124): Show | 127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2404-8753T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344206 | ||||||
chr8:22344427
|
A | G | 1 | a0001c0001t0004g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2404-8532A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344427 | ||||||
chr8:22344501
|
A | G | 5 | a0001c0001t0004g0216a0001c0001t0004g0217a0001c0001t0004g0218others(2): Show | 5 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404-8458A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344501 | ||||||
chr8:22344545
|
G | A | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-8414G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344545 | ||||||
chr8:22344555
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-8404G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344555 | ||||||
chr8:22344665
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2404-8294T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344665 | ||||||
chr8:22344803
|
G | T | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-8156G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344803 | ||||||
chr8:22344889
|
A | G | 2 | a0001c0001t0002g0060a0001c0001t0002g0061 | 2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2404-8070A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22344889 | ||||||
chr8:22345274
|
TTGTGTAC others(19): Show |
T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-7684_2404-765 others(30): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345274 | ||||||
chr8:22345292
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2404-7667T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345292 | ||||||
chr8:22345300
|
C | T | 124 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0086others(121): Show | 124 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.2404-7659C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345300 | ||||||
chr8:22345320
|
T | C | 4 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0157others(1): Show | 4 | HG02976.hp2 NA19060.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-7639T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345320 | ||||||
chr8:22345333
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0118 | 3 | HG00738.hp2 HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2404-7626G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345333 | ||||||
chr8:22345490
|
A | G | 12 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0149others(9): Show | 12 | HG00597.hp1 HG01109.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2404-7469A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345490 | ||||||
chr8:22345671
|
T | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(217): Show | 221 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(218): Show |
intron_variant | MODIFIER | c.2404-7288T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345671 | ||||||
chr8:22345786
|
C | T | 1 | a0001c0001t0004g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2404-7173C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345786 | ||||||
chr8:22345853
|
T | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-7106T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345853 | ||||||
chr8:22345863
|
A | T | 1 | a0001c0001t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2404-7096A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345863 | ||||||
chr8:22345884
|
C | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-7075C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345884 | ||||||
chr8:22345921
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(217): Show | 221 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(218): Show |
intron_variant | MODIFIER | c.2404-7038A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22345921 | ||||||
chr8:22346034
|
T | A | 4 | a0001c0001t0002g0090a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-6925T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346034 | ||||||
chr8:22346049
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2404-6910T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346049 | ||||||
chr8:22346251
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2404-6708A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346251 | ||||||
chr8:22346380
|
G | A | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2404-6579G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346380 | ||||||
chr8:22346568
|
T | G | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-6391T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346568 | ||||||
chr8:22346664
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2404-6295C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346664 | ||||||
chr8:22346793
|
G | T | 142 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(139): Show | 142 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.2404-6166G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346793 | ||||||
chr8:22346831
|
G | T | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-6128G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346831 | ||||||
chr8:22346994
|
A | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 9 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-5965A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22346994 | ||||||
chr8:22347161
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2404-5798C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347161 | ||||||
chr8:22347169
|
C | CA | 21 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(18): Show | 21 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.2404-5772dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347169 | |||||
chr8:22347169
|
CA | C | 18 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(15): Show | 18 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-5772delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347169 | |||||
chr8:22347213
|
A | AT | 24 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(21): Show | 24 | HG00597.hp2 HG01099.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.2404-5729dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347213 | |||||
chr8:22347269
|
G | A | 127 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(124): Show | 127 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2404-5690G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347269 | ||||||
chr8:22347281
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2404-5678C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347281 | ||||||
chr8:22347316
|
G | A | 1 | a0001c0001t0003g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2404-5643G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347316 | ||||||
chr8:22347514
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2404-5445G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347514 | ||||||
chr8:22347516
|
C | CT | 13 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0144others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2404-5419dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347516 | |||||
chr8:22347516
|
CT | C | 123 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0061others(120): Show | 123 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.2404-5419delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347516 | |||||
chr8:22347516
|
CTT | C | 15 | a0001c0001t0003g0265a0001c0001t0004g0190a0001c0001t0005g0006others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-5420_2404-541 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22347516 | |||||
chr8:22347578
|
G | T | 6 | a0001c0001t0003g0265a0001c0001t0004g0208a0001c0001t0004g0210others(3): Show | 6 | NA18950.hp2 NA18952.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-5381G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347578 | ||||||
chr8:22347776
|
C | T | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-5183C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347776 | ||||||
chr8:22347885
|
C | T | 1 | a0001c0001t0014g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2404-5074C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22347885 | ||||||
chr8:22348051
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2404-4908C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348051 | ||||||
chr8:22348088
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(31): Show | 35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2404-4871G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348088 | ||||||
chr8:22348125
|
A | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-4834A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348125 | ||||||
chr8:22348155
|
G | A | 7 | a0001c0001t0003g0265a0001c0001t0004g0208a0001c0001t0004g0210others(4): Show | 7 | NA18950.hp2 NA18952.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-4804G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348155 | ||||||
chr8:22348226
|
G | A | 2 | a0001c0001t0003g0255a0001c0001t0003g0285 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2404-4733G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348226 | ||||||
chr8:22348463
|
G | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2404-4496G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348463 | ||||||
chr8:22348512
|
C | T | 1 | a0001c0001t0004g0246 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2404-4447C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348512 | ||||||
chr8:22348525
|
G | A | 128 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(125): Show | 128 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2404-4434G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348525 | ||||||
chr8:22348922
|
C | T | 1 | a0001c0001t0029g0202 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2404-4037C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22348922 | ||||||
chr8:22349051
|
C | CT | 136 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0144others(133): Show | 136 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2404-3893dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349051 | |||||
chr8:22349051
|
C | CTT | 15 | a0001c0001t0004g0191a0001c0001t0005g0006a0001c0001t0005g0007others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2404-3894_2404-389 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349051 | |||||
chr8:22349118
|
T | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-3841T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349118 | ||||||
chr8:22349250
|
G | A | 128 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(125): Show | 128 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2404-3709G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349250 | ||||||
chr8:22349409
|
A | ATG | 34 | a0001c0001t0001g0087a0001c0001t0001g0119a0001c0001t0001g0120others(31): Show | 34 | HG00597.hp1 HG01109.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.2404-3540_2404-353 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349409 | |||||
chr8:22349409
|
ATG | A | 5 | a0001c0001t0004g0234a0001c0001t0004g0253a0001c0001t0010g0188others(2): Show | 5 | HG00597.hp2 HG00639.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-3540_2404-353 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349409 | |||||
chr8:22349415
|
G | GTA | 7 | a0001c0001t0003g0264a0001c0001t0004g0003a0001c0001t0004g0206others(4): Show | 7 | HG00558.hp1 HG00558.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | |||||
chr8:22349415
|
G | GTATA | 32 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(29): Show | 32 | HG00423.hp1 HG01257.hp2 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | |||||
chr8:22349415
|
G | GTATATA | 19 | a0001c0001t0003g0086a0001c0001t0003g0170a0001c0001t0003g0195others(16): Show | 19 | HG00609.hp1 HG01070.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | |||||
chr8:22349415
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0003g0225a0001c0001t0003g0275a0001c0001t0025g0172others(4): Show | 7 | HG01123.hp1 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-3543_2404-354 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | |||||
chr8:22349415
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0004g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2404-3543_2404-354 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | |||||
chr8:22349415
|
G | GTATATAT others(7): Show |
1 | a0003c0002t0012g0016 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2404-3543_2404-354 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | |||||
chr8:22349415
|
GTGTGTAT others(5): Show |
G | 4 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0272others(1): Show | 4 | NA18940.hp1 NA18964.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-3542_2404-353 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349415 | |||||
chr8:22349417
|
G | A | 129 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(126): Show | 129 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2404-3542G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349417 | ||||||
chr8:22349417
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG01106.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2404-3541_2404-354 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349417 | |||||
chr8:22349417
|
G | GTATATAT others(9): Show |
1 | a0001c0001t0003g0280 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2404-3541_2404-354 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349417 | |||||
chr8:22349419
|
G | A | 138 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0003g0002others(135): Show | 138 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.2404-3540G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349419 | ||||||
chr8:22349419
|
G | GTA | 9 | a0001c0001t0001g0165a0001c0001t0002g0036a0001c0001t0002g0037others(6): Show | 9 | HG00741.hp1 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-3515_2404-351 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | |||||
chr8:22349419
|
G | GTATGTAT others(27): Show |
1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-3537_2404-353 others(38): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | |||||
chr8:22349419
|
G | GTGTA | 3 | a0001c0001t0001g0027a0001c0001t0001g0124a0001c0001t0016g0148 | 3 | HG03516.hp1 NA18985.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2404-3539_2404-353 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | |||||
chr8:22349419
|
GTA | G | 4 | a0001c0001t0001g0115a0001c0001t0001g0183a0001c0001t0002g0062others(1): Show | 4 | HG01099.hp1 HG01258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-3515_2404-351 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22349419 | |||||
chr8:22349421
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 23 | HG00738.hp2 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2404-3538A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349421 | ||||||
chr8:22349423
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2404-3536A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349423 | ||||||
chr8:22349430
|
T | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-3529T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349430 | ||||||
chr8:22349445
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2404-3514_2404-351 others(19): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349445 | ||||||
chr8:22349601
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2404-3358C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349601 | ||||||
chr8:22349644
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-3315T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349644 | ||||||
chr8:22349857
|
T | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-3102T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22349857 | ||||||
chr8:22350018
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2404-2941G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350018 | ||||||
chr8:22350098
|
A | C | 3 | a0001c0001t0004g0253a0001c0001t0010g0188a0001c0001t0030g0193 | 3 | HG00639.hp1 HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2404-2861A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350098 | ||||||
chr8:22350107
|
G | A | 1 | a0001c0001t0004g0238 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2404-2852G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350107 | ||||||
chr8:22350286
|
C | CA | 16 | a0001c0001t0002g0065a0001c0001t0005g0006a0001c0001t0005g0007others(13): Show | 16 | HG00639.hp2 HG01069.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2404-2665dupA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22350286 | |||||
chr8:22350295
|
T | A | 1 | a0001c0001t0002g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2404-2664T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350295 | ||||||
chr8:22350541
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2404-2418G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350541 | ||||||
chr8:22350572
|
C | T | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-2387C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350572 | ||||||
chr8:22350582
|
A | G | 150 | a0001c0001t0001g0183a0001c0001t0001g0287a0001c0001t0001g0288others(147): Show | 150 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.2404-2377A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350582 | ||||||
chr8:22350886
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(250): Show | 254 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.2404-2073G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350886 | ||||||
chr8:22350915
|
C | T | 1 | a0001c0001t0007g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2404-2044C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350915 | ||||||
chr8:22350988
|
A | T | 7 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-1971A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22350988 | ||||||
chr8:22351048
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1911G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351048 | ||||||
chr8:22351079
|
T | A | 149 | a0001c0001t0001g0183a0001c0001t0001g0287a0001c0001t0001g0288others(146): Show | 149 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.2404-1880T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351079 | ||||||
chr8:22351146
|
G | A | 2 | a0001c0001t0004g0226a0010c0008t0004g0231 | 2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2404-1813G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351146 | ||||||
chr8:22351160
|
T | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(31): Show | 35 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.2404-1799T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351160 | ||||||
chr8:22351179
|
C | T | 1 | a0001c0001t0004g0003 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2404-1780C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351179 | ||||||
chr8:22351345
|
A | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0124others(15): Show | 18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-1614A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351345 | ||||||
chr8:22351432
|
C | CATATATA others(3): Show |
1 | a0001c0001t0003g0286 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2404-1524_2404-152 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351432 | |||||
chr8:22351432
|
C | CATATATA others(13): Show |
1 | a0002c0003t0003g0248 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2404-1524_2404-152 others(24): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351432 | |||||
chr8:22351435
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0003g0293 | 2 | HG03139.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2404-1524A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351435 | ||||||
chr8:22351436
|
C | CAT | 10 | a0001c0001t0001g0133a0001c0001t0003g0170a0001c0001t0003g0171others(7): Show | 10 | HG01069.hp2 HG01070.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-1521_2404-152 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATAT | 7 | a0001c0001t0002g0045a0001c0001t0003g0264a0001c0001t0003g0268others(4): Show | 7 | HG00558.hp1 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATAT | 10 | a0001c0001t0001g0119a0001c0001t0003g0276a0001c0001t0003g0280others(7): Show | 10 | HG00423.hp1 HG00735.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(1): Show |
13 | a0001c0001t0003g0260a0001c0001t0003g0277a0001c0001t0004g0003others(10): Show | 13 | HG00408.hp2 HG00609.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(3): Show |
14 | a0001c0001t0003g0271a0001c0001t0004g0181a0001c0001t0004g0200others(11): Show | 14 | HG01169.hp2 HG01346.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(5): Show |
12 | a0001c0001t0001g0120a0001c0001t0003g0258a0001c0001t0003g0263others(9): Show | 12 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(7): Show |
13 | a0001c0001t0003g0257a0001c0001t0003g0272a0001c0001t0003g0275others(10): Show | 13 | HG01257.hp2 HG01975.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(9): Show |
5 | a0001c0001t0001g0287a0001c0001t0003g0002a0001c0001t0003g0261others(2): Show | 5 | HG02622.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(11): Show |
7 | a0001c0001t0001g0167a0001c0001t0003g0004a0001c0001t0003g0262others(4): Show | 7 | HG00558.hp2 HG01978.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(13): Show |
4 | a0001c0001t0003g0237a0001c0001t0003g0255a0001c0001t0004g0211others(1): Show | 4 | HG02027.hp2 HG04199.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(24): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(15): Show |
4 | a0001c0001t0003g0278a0001c0001t0003g0289a0001c0001t0004g0199others(1): Show | 4 | HG04204.hp2 NA19009.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(19): Show |
2 | a0001c0001t0003g0256a0001c0001t0027g0005 | 2 | NA18942.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(30): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | CATATATA others(21): Show |
2 | a0001c0001t0003g0290a0001c0001t0003g0291 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2404-1520_2404-151 others(32): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
C | T | 2 | a0001c0001t0003g0286a0002c0003t0003g0248 | 2 | HG00597.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2404-1523C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351436 | ||||||
chr8:22351436
|
CATACATA others(3): Show |
C | 5 | a0001c0001t0003g0270a0001c0001t0006g0021a0001c0001t0006g0022others(2): Show | 5 | HG02717.hp1 HG03130.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.2404-1519_2404-151 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
CATACATA others(5): Show |
C | 3 | a0001c0001t0001g0288a0001c0001t0003g0259a0001c0001t0014g0164 | 3 | HG01358.hp2 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2404-1519_2404-150 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
CATACATA others(7): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1519_2404-150 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
CATACATA others(11): Show |
C | 1 | a0001c0001t0003g0284 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2404-1519_2404-150 others(22): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
CATACATA others(13): Show |
C | 2 | a0001c0001t0004g0206a0006c0012t0023g0247 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2404-1519_2404-150 others(24): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
CATACATA others(15): Show |
C | 19 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.2404-1519_2404-149 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
CATACATA others(21): Show |
C | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-1519_2404-149 others(32): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351436
|
CATACATA others(25): Show |
C | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1519_2404-148 others(36): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351436 | |||||
chr8:22351438
|
TAC | T | 3 | a0001c0001t0001g0134a0001c0001t0003g0225a0001c0001t0003g0269 | 3 | HG02630.hp1 NA18964.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2404-1519_2404-151 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351438 | |||||
chr8:22351440
|
C | CAT | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0126others(3): Show | 6 | HG01516.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404-1477_2404-147 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATAT | 10 | a0001c0001t0001g0132a0001c0001t0002g0025a0001c0001t0002g0032others(7): Show | 10 | HG00609.hp1 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2404-1479_2404-147 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATATATA others(1): Show |
8 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0114others(5): Show | 9 | HG00738.hp2 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.2404-1483_2404-147 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATATATA others(3): Show |
2 | a0001c0001t0002g0041a0001c0001t0011g0081 | 2 | HG03654.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2404-1485_2404-147 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATATATA others(5): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0169 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2404-1487_2404-147 others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATATATA others(7): Show |
2 | a0001c0001t0001g0088a0001c0001t0001g0108 | 2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2404-1489_2404-147 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATATATA others(9): Show |
2 | a0001c0001t0010g0188a0001c0001t0015g0079 | 2 | HG02145.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2404-1491_2404-147 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATATATA others(15): Show |
3 | a0001c0001t0001g0089a0001c0001t0001g0166a0001c0001t0003g0293 | 3 | HG02630.hp2 HG03209.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2404-1497_2404-147 others(26): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | CATATATA others(17): Show |
1 | a0001c0001t0001g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2404-1499_2404-147 others(28): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
C | T | 111 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(108): Show | 111 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.2404-1519C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351440 | ||||||
chr8:22351440
|
CAT | C | 19 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0002g0037others(16): Show | 19 | HG00408.hp1 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2404-1477_2404-147 others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATAT | C | 14 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0042others(11): Show | 14 | HG01074.hp1 HG01258.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.2404-1479_2404-147 others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATATAT | C | 3 | a0001c0001t0001g0163a0001c0001t0002g0052a0001c0001t0002g0080 | 3 | HG02135.hp2 NA18612.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2404-1481_2404-147 others(10): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATATATA others(1): Show |
C | 21 | a0001c0001t0002g0026a0001c0001t0002g0046a0001c0001t0002g0059others(18): Show | 21 | HG00423.hp2 HG00733.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.2404-1483_2404-147 others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATATATA others(3): Show |
C | 4 | a0001c0001t0002g0044a0001c0001t0002g0090a0001c0001t0002g0094others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-1485_2404-147 others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0002g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2404-1489_2404-147 others(18): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATATATA others(9): Show |
C | 1 | a0001c0001t0030g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2404-1491_2404-147 others(20): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0168 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2404-1499_2404-147 others(28): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351440
|
CATATATA others(19): Show |
C | 28 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(25): Show | 28 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.2404-1501_2404-147 others(30): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351440 | |||||
chr8:22351461
|
A | C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-1498A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351461 | ||||||
chr8:22351482
|
T | A | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1477T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351482 | ||||||
chr8:22351525
|
G | GT | 6 | a0001c0001t0001g0118a0001c0001t0002g0090a0001c0001t0003g0237others(3): Show | 6 | HG02109.hp2 HG02896.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2404-1424dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351525 | |||||
chr8:22351534
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1425T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351534 | ||||||
chr8:22351536
|
G | T | 7 | a0001c0001t0001g0183a0003c0002t0001g0019a0004c0004t0009g0174others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2404-1423G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351536 | ||||||
chr8:22351536
|
GT | G | 14 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(11): Show | 14 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2404-1416delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr8 | 22351536 | |||||
chr8:22351537
|
T | G | 1 | a0003c0002t0001g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2404-1422T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351537 | ||||||
chr8:22351538
|
T | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-1421T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351538 | ||||||
chr8:22351539
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2404-1420T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351539 | ||||||
chr8:22351540
|
T | G | 4 | a0004c0004t0009g0174a0004c0004t0009g0176a0004c0004t0009g0177others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404-1419T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351540 | ||||||
chr8:22351608
|
G | A | 4 | a0001c0001t0004g0191a0001c0001t0004g0197a0001c0001t0004g0198others(1): Show | 4 | HG01106.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2404-1351G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351608 | ||||||
chr8:22351726
|
C | T | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2404-1233C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351726 | ||||||
chr8:22351739
|
A | G | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-1220A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351739 | ||||||
chr8:22351796
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 9 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404-1163C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351796 | ||||||
chr8:22351804
|
G | T | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2404-1155G>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351804 | ||||||
chr8:22351806
|
T | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0124others(15): Show | 18 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2404-1153T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351806 | ||||||
chr8:22351829
|
G | A | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-1130G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351829 | ||||||
chr8:22351861
|
A | G | 1 | a0001c0001t0003g0279 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2404-1098A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22351861 | ||||||
chr8:22352161
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2404-798T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352161 | ||||||
chr8:22352383
|
G | A | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2404-576G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352383 | ||||||
chr8:22352399
|
C | G | 2 | a0001c0001t0004g0194a0001c0001t0004g0209 | 2 | HG00558.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.2404-560C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352399 | ||||||
chr8:22352417
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2404-542G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352417 | ||||||
chr8:22352451
|
T | C | 1 | a0001c0001t0003g0268 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2404-508T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352451 | ||||||
chr8:22352603
|
A | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2404-356A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352603 | ||||||
chr8:22352721
|
A | G | 150 | a0001c0001t0001g0183a0001c0001t0001g0287a0001c0001t0001g0288others(147): Show | 150 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.2404-238A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352721 | ||||||
chr8:22352739
|
T | G | 1 | a0001c0001t0002g0141 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2404-220T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352739 | ||||||
chr8:22352911
|
C | T | 1 | a0001c0001t0004g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2404-48C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352911 | ||||||
chr8:22352945
|
C | T | 1 | a0001c0001t0016g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2404-14C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 20/22 | chr8 | 22352945 | ||||||
chr8:22353292
|
GT | G | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2657+83delT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353292 | |||||
chr8:22353315
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2657+103G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353315 | ||||||
chr8:22353540
|
C | G | 1 | a0001c0001t0004g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2657+328C>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353540 | ||||||
chr8:22353607
|
C | T | 1 | a0001c0001t0004g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2657+395C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353607 | ||||||
chr8:22353723
|
G | A | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2657+511G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353723 | ||||||
chr8:22353743
|
A | G | 5 | a0003c0002t0001g0019a0003c0002t0012g0016a0003c0002t0012g0017others(2): Show | 5 | HG01099.hp2 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2658-528A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353743 | ||||||
chr8:22353764
|
C | CT | 54 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0087others(51): Show | 55 | HG00423.hp2 HG00733.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.2658-479dupT | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTT | 22 | a0001c0001t0001g0089a0001c0001t0001g0118a0001c0001t0001g0120others(19): Show | 22 | HG00597.hp1 HG01109.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.2658-480_2658-479d others(4): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTT | 7 | a0001c0001t0001g0124a0001c0001t0001g0144a0001c0001t0003g0291others(4): Show | 7 | HG02109.hp1 HG02970.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.2658-482_2658-479d others(6): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTT | 26 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0260others(23): Show | 26 | HG00558.hp1 HG01257.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.2658-483_2658-479d others(7): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTTT | 16 | a0001c0001t0003g0086a0001c0001t0003g0171a0001c0001t0003g0258others(13): Show | 16 | HG00423.hp1 HG00597.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2658-484_2658-479d others(8): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0183a0001c0001t0003g0266a0001c0001t0004g0217others(7): Show | 10 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2658-487_2658-479d others(11): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTTTT others(3): Show |
25 | a0001c0001t0003g0004a0001c0001t0004g0190a0001c0001t0004g0191others(22): Show | 25 | HG00609.hp2 HG00639.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2658-488_2658-479d others(12): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTTTT others(4): Show |
30 | a0001c0001t0003g0225a0001c0001t0003g0259a0001c0001t0004g0003others(27): Show | 30 | HG00408.hp2 HG00558.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.2658-489_2658-479d others(13): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTTTT others(5): Show |
10 | a0001c0001t0003g0195a0001c0001t0003g0196a0001c0001t0003g0215others(7): Show | 10 | HG00609.hp1 HG02027.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.2658-490_2658-479d others(14): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0006g0021a0001c0001t0010g0233a0001c0001t0014g0164others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2658-491_2658-479d others(15): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2658-492_2658-479d others(16): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353764
|
CTTTTTTT others(4): Show |
C | 15 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(12): Show | 15 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2658-489_2658-479d others(13): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | 22353764 | |||||
chr8:22353916
|
T | G | 21 | a0001c0001t0001g0027a0001c0001t0001g0119a0001c0001t0001g0120others(18): Show | 21 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.2658-355T>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353916 | ||||||
chr8:22353964
|
C | T | 1 | a0001c0001t0024g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2658-307C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353964 | ||||||
chr8:22353985
|
A | G | 1 | a0001c0001t0003g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2658-286A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22353985 | ||||||
chr8:22354073
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01891.hp2 HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2658-198G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22354073 | ||||||
chr8:22354144
|
T | C | 2 | a0001c0001t0010g0230a0001c0001t0010g0232 | 2 | NA18989.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2658-127T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22354144 | ||||||
chr8:22354243
|
T | A | 147 | a0001c0001t0001g0183a0001c0001t0002g0045a0001c0001t0003g0002others(144): Show | 147 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2658-28T>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 21/22 | chr8 | 22354243 | ||||||
chr8:22354430
|
C | CTAG | 8 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG00733.hp1 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2765+53_2765+55dup others(3): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 22354430 | |||||
chr8:22354614
|
C | T | 1 | a0003c0002t0012g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2765+236C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354614 | ||||||
chr8:22354629
|
A | T | 1 | a0001c0001t0003g0259 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2765+251A>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354629 | ||||||
chr8:22354690
|
A | G | 1 | a0006c0012t0023g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2765+312A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354690 | ||||||
chr8:22354773
|
C | T | 1 | a0001c0001t0028g0252 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2765+395C>T | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354773 | ||||||
chr8:22354798
|
G | A | 124 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0170others(121): Show | 124 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.2765+420G>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22354798 | ||||||
chr8:22355067
|
CA | C | 16 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2766-270delA | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 22355067 | |||||
chr8:22355086
|
A | G | 10 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2766-263A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355086 | ||||||
chr8:22355089
|
AAAC | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02004.hp1 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2766-248_2766-246d others(5): Show |
PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr8 | 22355089 | |||||
chr8:22355101
|
C | A | 16 | a0001c0001t0002g0067a0001c0001t0005g0006a0001c0001t0005g0007others(13): Show | 16 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2766-248C>A | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355101 | ||||||
chr8:22355104
|
A | C | 6 | a0001c0001t0003g0268a0001c0001t0004g0204a0004c0004t0009g0174others(3): Show | 6 | HG01891.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2766-245A>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355104 | ||||||
chr8:22355245
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2766-104G>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355245 | ||||||
chr8:22355265
|
A | G | 1 | a0001c0001t0008g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2766-84A>G | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355265 | ||||||
chr8:22355319
|
T | C | 1 | a0001c0001t0004g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2766-30T>C | PIWIL2 | ENSG00000197181.12 | transcript | ENST00000356766.11 | protein_coding | 22/22 | chr8 | 22355319 |