geneid | 257068 |
---|---|
ensemblid | ENSG00000240891.8 |
hgncid | 26462 |
symbol | PLCXD2 |
name | phosphatidylinositol specific phospholipase C X domain containing 2 |
refseq_nuc | NM_001413064.1 |
refseq_prot | NP_001399993.1 |
ensembl_nuc | ENST00000636933.2 |
ensembl_prot | ENSP00000490816.1 |
mane_status | MANE Select |
chr | chr3 |
start | 111674676 |
end | 111727007 |
strand | + |
ver | v1.2 |
region | chr3:111674676-111727007 |
region5000 | chr3:111669676-111732007 |
regionname0 | PLCXD2_chr3_111674676_111727007 |
regionname5000 | PLCXD2_chr3_111669676_111732007 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 341 | 312 | 83 | 61 | 112 | 14 | 40 | 91 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0002 | 0/0 | 341 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0003 | 0/0 | 341 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0004 | 0/0 | 341 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0005 | 0/0 | 341 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1026 | 310 | 83 | 60 | 112 | 13 | 40 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
c0002 | 0/0 | 1026 | 8 | 0 | 0 | 8 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
c0003 | 0/0 | 1026 | 2 | 0 | 1 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
c0004 | 0/0 | 1026 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
c0005 | 0/0 | 1026 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
c0006 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 6713 | 77 | 3 | 18 | 44 | 4 | 8 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0002 | 0/0 | 6701 | 64 | 0 | 12 | 41 | 2 | 9 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0003 | 0/1 | 6705 | 47 | 33 | 7 | 1 | 1 | 4 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0004 | 0/0 | 6701 | 37 | 15 | 7 | 6 | 2 | 7 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0005 | 0/0 | 6704 | 12 | 0 | 1 | 10 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0006 | 0/0 | 6717 | 12 | 0 | 5 | 6 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0007 | 1/0 | 6696 | 8 | 2 | 4 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0008 | 0/0 | 6705 | 6 | 6 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0009 | 0/0 | 6713 | 5 | 0 | 0 | 0 | 0 | 5 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0010 | 0/0 | 6713 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0011 | 0/0 | 6701 | 3 | 0 | 2 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0012 | 0/0 | 6709 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0013 | 0/0 | 6709 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0014 | 0/0 | 6705 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0015 | 0/0 | 6705 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0016 | 0/0 | 6709 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0017 | 0/0 | 6713 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0018 | 0/0 | 6713 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0019 | 0/0 | 6696 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0020 | 0/0 | 6705 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0021 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0022 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0023 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0024 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0025 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0026 | 0/0 | 6705 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0027 | 0/0 | 6705 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0028 | 0/0 | 6705 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0029 | 0/0 | 6705 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0030 | 0/0 | 6705 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0031 | 0/0 | 6705 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0032 | 0/0 | 6705 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0033 | 0/0 | 6709 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0034 | 0/0 | 6709 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0035 | 0/0 | 6709 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0036 | 0/0 | 6713 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0037 | 0/0 | 6713 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0038 | 0/0 | 6713 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0039 | 0/0 | 6713 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0040 | 0/0 | 6713 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0041 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0042 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0043 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0044 | 0/0 | 6713 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0045 | 0/0 | 6713 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0046 | 0/0 | 6713 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0047 | 0/0 | 6713 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0048 | 0/0 | 6713 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0049 | 0/0 | 6713 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0050 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0051 | 0/0 | 6701 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
t0052 | 0/0 | 6701 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 1 | 2 | 6 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0002 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0008 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0017 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1026 | 310 | 83 | 60 | 112 | 13 | 40 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0003 | 0/0 | 1026 | 2 | 0 | 1 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0002c0002 | 0/0 | 1026 | 8 | 0 | 0 | 8 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0003c0004 | 0/0 | 1026 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0004c0005 | 0/0 | 1026 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0005c0006 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7738 | 76 | 3 | 17 | 44 | 4 | 8 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0002 | 0/0 | 7726 | 56 | 0 | 12 | 33 | 2 | 9 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0003 | 0/1 | 7730 | 47 | 33 | 7 | 1 | 1 | 4 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0004 | 0/0 | 7726 | 37 | 15 | 7 | 6 | 2 | 7 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0005 | 0/0 | 7729 | 12 | 0 | 1 | 10 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0006 | 0/0 | 7742 | 12 | 0 | 5 | 6 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0007 | 1/0 | 7721 | 8 | 2 | 4 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0008 | 0/0 | 7730 | 6 | 6 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0009 | 0/0 | 7738 | 5 | 0 | 0 | 0 | 0 | 5 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0010 | 0/0 | 7738 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0011 | 0/0 | 7726 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0012 | 0/0 | 7734 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0013 | 0/0 | 7734 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0014 | 0/0 | 7730 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0015 | 0/0 | 7730 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0016 | 0/0 | 7734 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0017 | 0/0 | 7738 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0019 | 0/0 | 7721 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0020 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0021 | 0/0 | 7725 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0022 | 0/0 | 7725 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0023 | 0/0 | 7726 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0024 | 0/0 | 7726 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0025 | 0/0 | 7726 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0026 | 0/0 | 7730 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0027 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0028 | 0/0 | 7730 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0029 | 0/0 | 7730 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0030 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0031 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0032 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0033 | 0/0 | 7734 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0034 | 0/0 | 7734 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0035 | 0/0 | 7734 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0036 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0037 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0038 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0039 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0040 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0043 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0044 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0045 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0046 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0047 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0048 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0049 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0050 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0051 | 0/0 | 7726 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0001t0052 | 0/0 | 7726 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0001c0003t0011 | 0/0 | 7726 | 2 | 0 | 1 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0002c0002t0002 | 0/0 | 7726 | 7 | 0 | 0 | 7 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0002c0002t0042 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0003c0004t0002 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0003c0004t0041 | 0/0 | 7726 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0004c0005t0001 | 0/0 | 7738 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
a0005c0006t0018 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | copy fasta | chr3 | 111669676 | 111732007 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 1 | 2 | 6 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0017 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0007g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0007g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0009g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0012g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0013g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0013g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0013g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0014g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0015g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0016g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0017g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0019g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0021g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0022g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0023g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0024g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0025g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0026g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0027g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0028g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0029g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0030g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0031g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0032g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0033g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0034g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0035g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0036g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0037g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0038g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0039g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0040g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0043g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0044g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0045g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0046g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0047g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0048g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0049g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0050g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0051g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0001t0052g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0003t0011g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0001c0003t0011g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0002c0002t0042g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0003c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0003c0004t0041g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0004c0005t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
a0005c0006t0018g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00099 | hp2 | a0001 | c0001 | t0026 | g0045 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00140 | hp1 | a0001 | c0001 | t0040 | g0073 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00140 | hp2 | a0001 | c0003 | t0011 | g0182 | EUR | GBR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0008 | EUR | FIN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | FIN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00408 | hp1 | a0001 | c0001 | t0021 | g0236 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00609 | hp2 | a0003 | c0004 | t0041 | g0072 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00738 | hp2 | a0004 | c0005 | t0001 | g0056 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0170 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01081 | hp2 | a0001 | c0001 | t0028 | g0105 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01106 | hp1 | a0001 | c0001 | t0011 | g0244 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01168 | hp2 | a0001 | c0001 | t0013 | g0209 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01169 | hp2 | a0001 | c0001 | t0013 | g0208 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01192 | hp2 | a0001 | c0003 | t0011 | g0183 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01243 | hp2 | a0001 | c0001 | t0029 | g0115 | AMR | PUR | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0042 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0025 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0090 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0025 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01884 | hp2 | a0001 | c0001 | t0030 | g0265 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01934 | hp2 | a0001 | c0001 | t0013 | g0011 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0041 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0223 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0016 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01981 | hp2 | a0001 | c0001 | t0023 | g0002 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG01993 | hp2 | a0001 | c0001 | t0007 | g0112 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02027 | hp1 | a0001 | c0001 | t0046 | g0157 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02040 | hp2 | a0001 | c0001 | t0022 | g0207 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02055 | hp1 | a0001 | c0001 | t0025 | g0048 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0235 | EAS | CDX | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CDX | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02257 | hp1 | a0001 | c0001 | t0034 | g0054 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02258 | hp2 | a0001 | c0001 | t0014 | g0110 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02280 | hp2 | a0001 | c0001 | t0027 | g0262 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02300 | hp1 | a0001 | c0001 | t0007 | g0119 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02451 | hp2 | a0001 | c0001 | t0038 | g0250 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0261 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0123 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02647 | hp1 | a0001 | c0001 | t0031 | g0200 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02698 | hp1 | a0001 | c0001 | t0045 | g0228 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02717 | hp1 | a0001 | c0001 | t0036 | g0100 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02717 | hp2 | a0001 | c0001 | t0032 | g0201 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02735 | hp2 | a0001 | c0001 | t0052 | g0257 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02738 | hp2 | a0001 | c0001 | t0009 | g0135 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02809 | hp1 | a0005 | c0006 | t0018 | g0120 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02818 | hp2 | a0001 | c0001 | t0012 | g0197 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0221 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02895 | hp1 | a0001 | c0001 | t0033 | g0266 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03041 | hp2 | a0001 | c0001 | t0035 | g0057 | AFR | GWD | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03098 | hp2 | a0001 | c0001 | t0017 | g0106 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0037 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0225 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03209 | hp2 | a0001 | c0001 | t0019 | g0036 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03225 | hp2 | a0001 | c0001 | t0016 | g0253 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03239 | hp2 | a0001 | c0001 | t0051 | g0122 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03453 | hp1 | a0001 | c0001 | t0020 | g0051 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0226 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0247 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03669 | hp2 | a0001 | c0001 | t0049 | g0169 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03704 | hp1 | a0001 | c0001 | t0009 | g0186 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0206 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03834 | hp2 | a0001 | c0001 | t0009 | g0139 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0155 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0038 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03942 | hp1 | a0001 | c0001 | t0039 | g0222 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG04115 | hp2 | a0001 | c0001 | t0009 | g0111 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | STU | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18945 | hp2 | a0001 | c0001 | t0010 | g0066 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18966 | hp1 | a0002 | c0002 | t0042 | g0070 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18968 | hp1 | a0003 | c0004 | t0002 | g0021 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18968 | hp2 | a0001 | c0001 | t0047 | g0163 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18975 | hp2 | a0001 | c0001 | t0010 | g0187 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18979 | hp2 | a0001 | c0001 | t0037 | g0175 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18988 | hp1 | a0001 | c0001 | t0044 | g0075 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19002 | hp2 | a0001 | c0001 | t0010 | g0077 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19009 | hp2 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19081 | hp1 | a0001 | c0001 | t0010 | g0076 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19084 | hp1 | a0001 | c0001 | t0050 | g0210 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19084 | hp2 | a0001 | c0001 | t0043 | g0162 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19091 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | YRI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ASW | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ASW | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20805 | hp1 | a0001 | c0001 | t0048 | g0129 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0227 | SAS | GIH | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0113 | SAS | GIH | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02109 | hp2 | a0001 | c0001 | t0015 | g0260 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02559 | hp1 | a0001 | c0001 | t0015 | g0050 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0198 | AFR | ACB | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0199 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | USA | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
NA21309 | hp2 | a0001 | c0001 | t0024 | g0194 | AFR | LWK | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0017 | REF | REF | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0204 | REF | REF | PLCXD2_chr3_111669676_111732007 | PLCXD2 | chr3 | 111669676 | 111732007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:111675366
|
C | G | 2 | a0002a0003 | 10 | HG00609.hp2 NA18945.hp1 NA18955.hp1 others(7): Show |
missense_variant | MODERATE | c.121C>G | p.Pro41Ala | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 691/7721 | 121/1026 | 41/341 | chr3 | 111675366 | ||
chr3:111708093
|
C | T | 1 | a0004 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.331C>T | p.Arg111Cys | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/4 | 901/7721 | 331/1026 | 111/341 | chr3 | 111708093 | ||
chr3:111713905
|
T | C | 1 | a0002 | 8 | NA18945.hp1 NA18955.hp1 NA18966.hp1 others(5): Show |
missense_variant | MODERATE | c.643T>C | p.Cys215Arg | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/4 | 1213/7721 | 643/1026 | 215/341 | chr3 | 111713905 | ||
chr3:111713957
|
C | T | 1 | a0005 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.695C>T | p.Ala232Val | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/4 | 1265/7721 | 695/1026 | 232/341 | chr3 | 111713957 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:111675401
|
A | G | 1 | a0005c0006 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.156A>G | p.Ala52Ala | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 726/7721 | 156/1026 | 52/341 | chr3 | 111675401 | ||
chr3:111713958
|
G | A | 1 | a0001c0003 | 2 | HG00140.hp2 HG01192.hp2 |
synonymous_variant | LOW | c.696G>A | p.Ala232Ala | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/4 | 1266/7721 | 696/1026 | 232/341 | chr3 | 111713958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:111674834
|
C | T | 1 | a0001c0001t0052 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-412C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 412 | chr3 | 111674834 | |||||
chr3:111674954
|
A | C | 1 | a0001c0001t0051 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-292A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/4 | 292 | chr3 | 111674954 | |||||
chr3:111720926
|
G | A | 1 | a0005c0006t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 44 | chr3 | 111720926 | |||||
chr3:111721030
|
A | G | 1 | a0001c0001t0009 | 5 | HG02738.hp2 HG03704.hp1 HG03834.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*148A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 148 | chr3 | 111721030 | |||||
chr3:111721053
|
G | C | 1 | a0001c0001t0010 | 4 | NA18945.hp2 NA18975.hp2 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*171G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 171 | chr3 | 111721053 | |||||
chr3:111721107
|
C | T | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*225C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 225 | chr3 | 111721107 | |||||
chr3:111721378
|
A | G | 1 | a0001c0001t0050 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 496 | chr3 | 111721378 | |||||
chr3:111721629
|
T | G | 1 | a0001c0001t0020 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*747T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 747 | chr3 | 111721629 | |||||
chr3:111721842
|
C | T | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*960C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 960 | chr3 | 111721842 | |||||
chr3:111721979
|
G | A | 1 | a0001c0001t0040 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1097G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1097 | chr3 | 111721979 | |||||
chr3:111722128
|
AT | A | 3 | a0001c0001t0005a0001c0001t0021a0001c0001t0022 | 14 | HG00408.hp1 HG01952.hp2 HG02040.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1256delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1256 | INFO_REALIGN_3_PRIME | chr3 | 111722128 | ||||
chr3:111722141
|
C | T | 1 | a0001c0001t0049 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1259 | chr3 | 111722141 | |||||
chr3:111722164
|
G | A | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*1282G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1282 | chr3 | 111722164 | |||||
chr3:111722182
|
G | GATTGACT others(1): Show |
6 | a0001c0001t0012a0001c0001t0013a0001c0001t0016others(3): Show | 11 | HG01168.hp2 HG01169.hp2 HG01934.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722182 | ||||
chr3:111722182
|
G | GATTGACT others(5): Show |
17 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(14): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT others(8): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722182 | ||||
chr3:111722182
|
G | GATTGACT others(9): Show |
1 | a0001c0001t0006 | 12 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT others(12): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722182 | ||||
chr3:111722184
|
T | TTGAC | 13 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(10): Show | 77 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1303_*1304insGACT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | INFO_REALIGN_3_PRIME | chr3 | 111722184 | ||||
chr3:111722186
|
T | G | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(13): Show | 114 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1304T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1304 | chr3 | 111722186 | |||||
chr3:111722188
|
T | C | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(13): Show | 114 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1306T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1306 | chr3 | 111722188 | |||||
chr3:111722190
|
T | G | 1 | a0001c0001t0022 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1308 | chr3 | 111722190 | |||||
chr3:111722192
|
T | C | 1 | a0001c0001t0022 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1310 | chr3 | 111722192 | |||||
chr3:111722213
|
T | G | 1 | a0001c0001t0044 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1331 | chr3 | 111722213 | |||||
chr3:111722227
|
T | C | 1 | a0001c0001t0026 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1345 | chr3 | 111722227 | |||||
chr3:111722368
|
C | G | 3 | a0001c0001t0012a0001c0001t0017a0001c0001t0032 | 6 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1486C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1486 | chr3 | 111722368 | |||||
chr3:111722407
|
A | G | 1 | a0001c0001t0025 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1525A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1525 | chr3 | 111722407 | |||||
chr3:111722477
|
G | A | 3 | a0001c0001t0014a0001c0001t0036a0005c0006t0018 | 4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1595G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1595 | chr3 | 111722477 | |||||
chr3:111722570
|
T | G | 1 | a0001c0001t0023 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1688T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1688 | chr3 | 111722570 | |||||
chr3:111722825
|
G | A | 11 | a0001c0001t0003a0001c0001t0005a0001c0001t0016others(8): Show | 69 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1943G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 1943 | chr3 | 111722825 | |||||
chr3:111723213
|
G | T | 1 | a0001c0001t0039 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2331 | chr3 | 111723213 | |||||
chr3:111723467
|
A | G | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2585A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2585 | chr3 | 111723467 | |||||
chr3:111723483
|
C | G | 1 | a0001c0001t0038 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2601C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2601 | chr3 | 111723483 | |||||
chr3:111723505
|
G | A | 1 | a0001c0001t0027 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2623G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2623 | chr3 | 111723505 | |||||
chr3:111723765
|
G | A | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2883G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 2883 | chr3 | 111723765 | |||||
chr3:111723949
|
G | A | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3067G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3067 | chr3 | 111723949 | |||||
chr3:111723970
|
C | T | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*3088C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3088 | chr3 | 111723970 | |||||
chr3:111724076
|
T | A | 3 | a0001c0001t0012a0001c0001t0017a0001c0001t0032 | 6 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3194T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3194 | chr3 | 111724076 | |||||
chr3:111724112
|
A | G | 5 | a0001c0001t0004a0001c0001t0023a0001c0001t0025others(2): Show | 41 | HG00639.hp2 HG01071.hp2 HG01168.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3230A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3230 | chr3 | 111724112 | |||||
chr3:111724147
|
G | A | 3 | a0001c0001t0014a0001c0001t0036a0005c0006t0018 | 4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3265G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3265 | chr3 | 111724147 | |||||
chr3:111724156
|
A | G | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(31): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*3274A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3274 | chr3 | 111724156 | |||||
chr3:111724484
|
T | C | 1 | a0001c0001t0028 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3602T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3602 | chr3 | 111724484 | |||||
chr3:111724801
|
T | G | 1 | a0001c0001t0029 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 3919 | chr3 | 111724801 | |||||
chr3:111724900
|
T | C | 5 | a0001c0001t0004a0001c0001t0023a0001c0001t0025others(2): Show | 41 | HG00639.hp2 HG01071.hp2 HG01168.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4018T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4018 | chr3 | 111724900 | |||||
chr3:111724920
|
A | C | 1 | a0002c0002t0042 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4038A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4038 | chr3 | 111724920 | |||||
chr3:111724937
|
C | A | 1 | a0001c0001t0039 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4055C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4055 | chr3 | 111724937 | |||||
chr3:111724984
|
G | C | 3 | a0001c0001t0014a0001c0001t0036a0005c0006t0018 | 4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4102G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4102 | chr3 | 111724984 | |||||
chr3:111725216
|
T | C | 1 | a0001c0001t0026 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4334T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4334 | chr3 | 111725216 | |||||
chr3:111725247
|
C | G | 1 | a0001c0001t0030 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4365C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4365 | chr3 | 111725247 | |||||
chr3:111725470
|
C | A | 1 | a0003c0004t0041 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4588C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4588 | chr3 | 111725470 | |||||
chr3:111725634
|
C | T | 6 | a0001c0001t0012a0001c0001t0014a0001c0001t0017others(3): Show | 10 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4752C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 4752 | chr3 | 111725634 | |||||
chr3:111725952
|
G | A | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*5070G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5070 | chr3 | 111725952 | |||||
chr3:111726039
|
C | T | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(12): Show | 113 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*5157C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5157 | chr3 | 111726039 | |||||
chr3:111726058
|
T | TACCTG | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*5178_*5179insCTGA others(1): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5179 | INFO_REALIGN_3_PRIME | chr3 | 111726058 | ||||
chr3:111726130
|
C | A | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(11): Show | 112 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*5248C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5248 | chr3 | 111726130 | |||||
chr3:111726142
|
C | T | 1 | a0001c0001t0047 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5260C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5260 | chr3 | 111726142 | |||||
chr3:111726188
|
G | A | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*5306G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5306 | chr3 | 111726188 | |||||
chr3:111726325
|
T | C | 1 | a0001c0001t0033 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5443T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5443 | chr3 | 111726325 | |||||
chr3:111726424
|
G | C | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*5542G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5542 | chr3 | 111726424 | |||||
chr3:111726424
|
G | T | 2 | a0001c0001t0008a0001c0001t0035 | 7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5542G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5542 | chr3 | 111726424 | |||||
chr3:111726493
|
G | C | 1 | a0001c0001t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5611G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5611 | chr3 | 111726493 | |||||
chr3:111726573
|
G | A | 1 | a0001c0001t0045 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5691G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5691 | chr3 | 111726573 | |||||
chr3:111726699
|
T | C | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(11): Show | 112 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*5817T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5817 | chr3 | 111726699 | |||||
chr3:111726820
|
T | G | 5 | a0001c0001t0005a0001c0001t0021a0001c0001t0022others(2): Show | 16 | HG00408.hp1 HG01952.hp2 HG02027.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5938T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5938 | chr3 | 111726820 | |||||
chr3:111726865
|
G | A | 1 | a0001c0001t0014 | 2 | HG02258.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5983G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 4/4 | 5983 | chr3 | 111726865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:111675559
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.163+151G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675559 | ||||||
chr3:111675694
|
T | G | 1 | a0002c0002t0002g0035 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.163+286T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675694 | ||||||
chr3:111675772
|
CACAA | C | 7 | a0001c0001t0004g0014a0001c0001t0004g0263a0001c0001t0004g0264others(4): Show | 9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+369_163+372del others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111675772 | |||||
chr3:111675857
|
A | G | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+449A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675857 | ||||||
chr3:111675882
|
G | A | 7 | a0001c0001t0004g0014a0001c0001t0004g0263a0001c0001t0004g0264others(4): Show | 9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+474G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111675882 | ||||||
chr3:111676130
|
G | T | 3 | a0001c0001t0003g0033a0001c0001t0003g0258a0001c0001t0003g0259 | 4 | HG02922.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+722G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676130 | ||||||
chr3:111676325
|
A | T | 1 | a0001c0001t0052g0257 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.163+917A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676325 | ||||||
chr3:111676360
|
G | A | 2 | a0001c0001t0014g0037a0001c0001t0019g0036 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.163+952G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676360 | ||||||
chr3:111676549
|
C | T | 9 | a0001c0001t0003g0032a0001c0001t0003g0249a0001c0001t0003g0251others(6): Show | 10 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+1141C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676549 | ||||||
chr3:111676578
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.163+1170G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676578 | ||||||
chr3:111676671
|
T | G | 1 | a0001c0001t0006g0039 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.163+1263T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676671 | ||||||
chr3:111676707
|
A | G | 7 | a0001c0001t0001g0242a0001c0001t0001g0245a0001c0001t0001g0246others(4): Show | 7 | HG00639.hp2 HG01106.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+1299A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676707 | ||||||
chr3:111676721
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(215): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.163+1313T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676721 | ||||||
chr3:111676761
|
T | G | 1 | a0001c0001t0001g0015 | 2 | HG02080.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.163+1353T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676761 | ||||||
chr3:111676864
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.163+1456G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676864 | ||||||
chr3:111676999
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0006g0016a0001c0001t0006g0041others(1): Show | 4 | HG01358.hp1 HG01943.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+1591G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111676999 | ||||||
chr3:111677033
|
G | A | 1 | a0001c0001t0003g0043 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.163+1625G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677033 | ||||||
chr3:111677378
|
G | A | 5 | a0001c0001t0004g0014a0001c0001t0004g0263a0001c0001t0004g0264others(2): Show | 7 | HG02280.hp2 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1970G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677378 | ||||||
chr3:111677543
|
G | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2135G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677543 | ||||||
chr3:111677916
|
G | A | 9 | a0001c0001t0003g0032a0001c0001t0003g0249a0001c0001t0003g0251others(6): Show | 10 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+2508G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677916 | ||||||
chr3:111677920
|
G | A | 5 | a0001c0001t0004g0014a0001c0001t0004g0263a0001c0001t0004g0264others(2): Show | 7 | HG02280.hp2 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+2512G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111677920 | ||||||
chr3:111678129
|
C | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+2721C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111678129 | ||||||
chr3:111678639
|
G | A | 1 | a0001c0001t0003g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.163+3231G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111678639 | ||||||
chr3:111679075
|
G | GT | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+3674dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111679075 | |||||
chr3:111679082
|
T | TA | 6 | a0001c0001t0003g0017a0001c0001t0004g0002a0001c0001t0004g0044others(3): Show | 9 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+3679dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111679082 | |||||
chr3:111679357
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(220): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.163+3949T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679357 | ||||||
chr3:111679375
|
G | T | 1 | a0001c0001t0002g0241 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.163+3967G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679375 | ||||||
chr3:111679536
|
A | T | 1 | a0001c0001t0002g0193 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.163+4128A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679536 | ||||||
chr3:111679588
|
G | A | 2 | a0001c0001t0005g0202a0001c0001t0005g0203 | 2 | NA19003.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.163+4180G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679588 | ||||||
chr3:111679774
|
G | A | 10 | a0001c0001t0003g0032a0001c0001t0003g0249a0001c0001t0003g0251others(7): Show | 11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+4366G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679774 | ||||||
chr3:111679777
|
G | A | 14 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0195others(11): Show | 20 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.163+4369G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111679777 | ||||||
chr3:111680021
|
G | A | 1 | a0001c0001t0003g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.163+4613G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680021 | ||||||
chr3:111680041
|
A | T | 16 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0195others(13): Show | 22 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.163+4633A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680041 | ||||||
chr3:111680228
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0003g0192 | 2 | HG01496.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.163+4820A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680228 | ||||||
chr3:111680268
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(95): Show | 117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.163+4860A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680268 | ||||||
chr3:111680362
|
C | T | 91 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0059others(88): Show | 110 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.163+4954C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680362 | ||||||
chr3:111680457
|
TG | T | 3 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199 | 3 | HG02559.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.163+5050delG | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680457 | ||||||
chr3:111680487
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(268): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.163+5079C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680487 | ||||||
chr3:111680571
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(220): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.163+5163A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680571 | ||||||
chr3:111680720
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.163+5312A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680720 | ||||||
chr3:111680762
|
T | C | 16 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0195others(13): Show | 22 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.163+5354T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680762 | ||||||
chr3:111680845
|
T | A | 2 | a0001c0001t0030g0265a0001c0001t0033g0266 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.163+5437T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111680845 | ||||||
chr3:111681010
|
C | CA | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+5608dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111681010 | |||||
chr3:111681081
|
A | G | 6 | a0001c0001t0002g0237a0001c0001t0005g0235a0001c0001t0005g0238others(3): Show | 6 | HG00408.hp1 HG02040.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+5673A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681081 | ||||||
chr3:111681096
|
T | C | 1 | a0001c0001t0035g0057 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163+5688T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681096 | ||||||
chr3:111681178
|
C | T | 1 | a0001c0001t0002g0190 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.163+5770C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681178 | ||||||
chr3:111681315
|
C | T | 15 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0195others(12): Show | 21 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+5907C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681315 | ||||||
chr3:111681440
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.163+6032T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681440 | ||||||
chr3:111681548
|
C | T | 1 | a0001c0001t0003g0256 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163+6140C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681548 | ||||||
chr3:111681651
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(95): Show | 117 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.163+6243T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681651 | ||||||
chr3:111681799
|
T | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0059others(56): Show | 77 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.163+6391T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681799 | ||||||
chr3:111681856
|
C | T | 2 | a0001c0001t0001g0055a0004c0005t0001g0056 | 2 | HG00738.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.163+6448C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681856 | ||||||
chr3:111681933
|
C | A | 2 | a0001c0001t0014g0037a0001c0001t0019g0036 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.163+6525C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681933 | ||||||
chr3:111681993
|
C | T | 1 | a0001c0001t0003g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.163+6585C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111681993 | ||||||
chr3:111682091
|
G | A | 2 | a0001c0001t0003g0096a0001c0001t0004g0097 | 2 | HG00735.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.163+6683G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682091 | ||||||
chr3:111682142
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.163+6734G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682142 | ||||||
chr3:111682268
|
A | G | 1 | a0001c0001t0005g0234 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.163+6860A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682268 | ||||||
chr3:111682364
|
T | A | 1 | a0001c0001t0012g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.163+6956T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682364 | ||||||
chr3:111682372
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.163+6964T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682372 | ||||||
chr3:111682893
|
C | T | 2 | a0001c0001t0002g0189a0001c0001t0052g0257 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.163+7485C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682893 | ||||||
chr3:111682979
|
A | T | 1 | a0001c0001t0034g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.163+7571A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682979 | ||||||
chr3:111682993
|
C | T | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+7585C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111682993 | ||||||
chr3:111683002
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0003g0049a0001c0001t0015g0050others(3): Show | 6 | HG00738.hp2 HG01517.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+7594G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683002 | ||||||
chr3:111683050
|
C | T | 1 | a0001c0001t0020g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.163+7642C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683050 | ||||||
chr3:111683088
|
A | C | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.163+7680A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683088 | ||||||
chr3:111683110
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.163+7702G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683110 | ||||||
chr3:111683156
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163+7748A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683156 | ||||||
chr3:111683184
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.163+7776T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683184 | ||||||
chr3:111683215
|
T | C | 6 | a0001c0001t0001g0055a0001c0001t0003g0049a0001c0001t0015g0050others(3): Show | 6 | HG00738.hp2 HG01517.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+7807T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683215 | ||||||
chr3:111683218
|
C | T | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163+7810C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683218 | ||||||
chr3:111683531
|
T | A | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163+8123T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683531 | ||||||
chr3:111683637
|
A | G | 1 | a0001c0001t0003g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.163+8229A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683637 | ||||||
chr3:111683715
|
A | G | 5 | a0001c0001t0003g0047a0001c0001t0003g0125a0001c0001t0004g0124others(2): Show | 5 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+8307A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683715 | ||||||
chr3:111683753
|
A | G | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+8345A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683753 | ||||||
chr3:111683849
|
C | T | 2 | a0001c0001t0014g0037a0001c0001t0019g0036 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.163+8441C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683849 | ||||||
chr3:111683851
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.163+8443C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111683851 | ||||||
chr3:111684056
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.163+8648G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684056 | ||||||
chr3:111684175
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163+8767C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684175 | ||||||
chr3:111684327
|
T | TA | 21 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0002g0189others(18): Show | 27 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.163+8938dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111684327 | |||||
chr3:111684327
|
TA | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0121a0001c0001t0001g0130others(6): Show | 9 | HG01515.hp2 HG02040.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.163+8938delA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111684327 | |||||
chr3:111684377
|
G | A | 1 | a0001c0001t0032g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+8969G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684377 | ||||||
chr3:111684403
|
C | G | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+8995C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684403 | ||||||
chr3:111684451
|
TGAGACTA others(90): Show |
T | 1 | a0001c0001t0002g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.163+9050_163+9146d others(99): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111684451 | |||||
chr3:111684527
|
G | A | 6 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0136others(3): Show | 6 | HG03017.hp1 HG03041.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+9119G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684527 | ||||||
chr3:111684668
|
T | A | 6 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(3): Show | 7 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+9260T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684668 | ||||||
chr3:111684703
|
A | C | 1 | a0001c0001t0005g0239 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.163+9295A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111684703 | ||||||
chr3:111685037
|
G | T | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+9629G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685037 | ||||||
chr3:111685120
|
A | C | 1 | a0001c0001t0006g0188 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.163+9712A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685120 | ||||||
chr3:111685164
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0006g0232 | 2 | HG01978.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.163+9756C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685164 | ||||||
chr3:111685207
|
A | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+9799A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685207 | ||||||
chr3:111685263
|
C | T | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163+9855C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685263 | ||||||
chr3:111685636
|
A | G | 1 | a0001c0001t0016g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.163+10228A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685636 | ||||||
chr3:111685656
|
T | C | 12 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0003g0101others(9): Show | 12 | HG01081.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+10248T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685656 | ||||||
chr3:111685916
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.163+10508C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685916 | ||||||
chr3:111685962
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163+10554T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111685962 | ||||||
chr3:111686021
|
C | T | 1 | a0001c0001t0010g0187 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.163+10613C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686021 | ||||||
chr3:111686163
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.163+10755A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686163 | ||||||
chr3:111686175
|
T | C | 1 | a0001c0001t0033g0266 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.163+10767T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686175 | ||||||
chr3:111686250
|
C | T | 10 | a0001c0001t0003g0032a0001c0001t0003g0249a0001c0001t0003g0251others(7): Show | 11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+10842C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686250 | ||||||
chr3:111686468
|
T | G | 8 | a0001c0001t0004g0012a0001c0001t0004g0029a0001c0001t0004g0030others(5): Show | 12 | HG01168.hp2 HG01169.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+11060T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686468 | ||||||
chr3:111686504
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.163+11096T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686504 | ||||||
chr3:111686560
|
G | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0058others(106): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.163+11152G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686560 | ||||||
chr3:111686769
|
T | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(251): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.163+11361T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686769 | ||||||
chr3:111686868
|
A | C | 1 | a0001c0001t0005g0224 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.163+11460A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686868 | ||||||
chr3:111686951
|
G | A | 1 | a0001c0001t0021g0236 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.163+11543G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111686951 | ||||||
chr3:111687064
|
C | T | 95 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0059others(92): Show | 114 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.163+11656C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687064 | ||||||
chr3:111687068
|
G | A | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+11660G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687068 | ||||||
chr3:111687097
|
T | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(98): Show | 122 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.163+11689T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687097 | ||||||
chr3:111687179
|
T | A | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+11771T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687179 | ||||||
chr3:111687241
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(84): Show | 105 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.163+11833A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687241 | ||||||
chr3:111687449
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.163+12041G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687449 | ||||||
chr3:111687570
|
A | T | 1 | a0001c0001t0009g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.163+12162A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687570 | ||||||
chr3:111687661
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.163+12253A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687661 | ||||||
chr3:111687665
|
G | GT | 17 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(14): Show | 18 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+12263dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111687665 | |||||
chr3:111687684
|
CT | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(99): Show | 123 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.163+12290delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111687684 | |||||
chr3:111687687
|
T | TC | 3 | a0001c0001t0030g0265a0001c0001t0031g0200a0001c0001t0033g0266 | 3 | HG01884.hp2 HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.163+12279_163+1228 others(5): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687687 | ||||||
chr3:111687688
|
T | C | 20 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0121others(17): Show | 21 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+12280T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687688 | ||||||
chr3:111687689
|
T | C | 3 | a0001c0001t0003g0043a0001c0001t0009g0139a0001c0001t0009g0186 | 3 | HG01257.hp1 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.163+12281T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687689 | ||||||
chr3:111687748
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(222): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.163+12340G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687748 | ||||||
chr3:111687813
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163+12405T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111687813 | ||||||
chr3:111688045
|
G | C | 1 | a0001c0001t0003g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.163+12637G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688045 | ||||||
chr3:111688317
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163+12909C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688317 | ||||||
chr3:111688335
|
G | A | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+12927G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688335 | ||||||
chr3:111688451
|
G | A | 2 | a0001c0001t0030g0265a0001c0001t0033g0266 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.163+13043G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688451 | ||||||
chr3:111688463
|
T | C | 2 | a0001c0001t0004g0024a0001c0001t0004g0141 | 3 | HG01168.hp1 HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.163+13055T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688463 | ||||||
chr3:111688646
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0008g0052a0001c0001t0008g0053 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+13238C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688646 | ||||||
chr3:111688719
|
C | T | 1 | a0002c0002t0002g0010 | 3 | NA18945.hp1 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.163+13311C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688719 | ||||||
chr3:111688807
|
C | T | 16 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(13): Show | 17 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+13399C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688807 | ||||||
chr3:111688854
|
CAAT | C | 8 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0049others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+13447_163+1344 others(7): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111688854 | ||||||
chr3:111688893
|
T | TTA | 3 | a0001c0001t0001g0086a0001c0001t0002g0087a0001c0001t0003g0256 | 3 | HG01255.hp2 HG03098.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.163+13498_163+1349 others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111688893 | |||||
chr3:111689044
|
A | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(12): Show | 16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.163+13636A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111689044 | ||||||
chr3:111689341
|
C | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(268): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.163+13933C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111689341 | ||||||
chr3:111689623
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.163+14215G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111689623 | ||||||
chr3:111689708
|
G | A | 2 | a0001c0001t0008g0052a0001c0001t0008g0053 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.163+14300G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111689708 | ||||||
chr3:111690119
|
A | G | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+14711A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690119 | ||||||
chr3:111690134
|
T | TA | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(124): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.163+14731dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111690134 | |||||
chr3:111690251
|
G | A | 3 | a0001c0001t0003g0033a0001c0001t0003g0258a0001c0001t0003g0259 | 4 | HG02922.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+14843G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690251 | ||||||
chr3:111690478
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163+15070G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690478 | ||||||
chr3:111690631
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0008g0052a0001c0001t0008g0053 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+15223C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690631 | ||||||
chr3:111690727
|
C | T | 5 | a0001c0001t0004g0014a0001c0001t0004g0263a0001c0001t0004g0264others(2): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+15319C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111690727 | ||||||
chr3:111691050
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0006g0039 | 2 | NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.163+15642T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691050 | ||||||
chr3:111691072
|
AAAG | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0049others(3): Show | 6 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+15668_163+1567 others(7): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111691072 | |||||
chr3:111691177
|
C | T | 3 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196 | 4 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+15769C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691177 | ||||||
chr3:111691200
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0008g0052a0001c0001t0008g0053 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+15792T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691200 | ||||||
chr3:111691214
|
G | C | 3 | a0001c0001t0001g0034a0001c0001t0008g0052a0001c0001t0008g0053 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.163+15806G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691214 | ||||||
chr3:111691235
|
A | G | 1 | a0001c0001t0032g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+15827A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691235 | ||||||
chr3:111691690
|
A | G | 1 | a0001c0001t0002g0009 | 3 | HG00733.hp1 HG00735.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.164-16236A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691690 | ||||||
chr3:111691902
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.164-16024A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691902 | ||||||
chr3:111691962
|
C | A | 1 | a0001c0001t0003g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-15964C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691962 | ||||||
chr3:111691976
|
A | C | 3 | a0001c0001t0001g0034a0001c0001t0008g0052a0001c0001t0008g0053 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-15950A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111691976 | ||||||
chr3:111692041
|
G | T | 3 | a0001c0001t0001g0034a0001c0001t0008g0052a0001c0001t0008g0053 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-15885G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692041 | ||||||
chr3:111692187
|
A | G | 15 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(12): Show | 16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-15739A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692187 | ||||||
chr3:111692294
|
C | T | 2 | a0001c0001t0003g0256a0001c0001t0007g0119 | 2 | HG02300.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.164-15632C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692294 | ||||||
chr3:111692337
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.164-15589G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692337 | ||||||
chr3:111692420
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-15506A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692420 | ||||||
chr3:111692543
|
G | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(223): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.164-15383G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692543 | ||||||
chr3:111692677
|
A | C | 1 | a0001c0001t0003g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.164-15249A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692677 | ||||||
chr3:111692965
|
C | T | 15 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(12): Show | 16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-14961C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111692965 | ||||||
chr3:111693015
|
G | A | 5 | a0001c0001t0001g0059a0001c0001t0002g0006a0001c0001t0002g0062others(2): Show | 7 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-14911G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693015 | ||||||
chr3:111693300
|
T | C | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.164-14626T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693300 | ||||||
chr3:111693419
|
C | T | 1 | a0001c0001t0009g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.164-14507C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693419 | ||||||
chr3:111693426
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(84): Show | 105 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.164-14500C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693426 | ||||||
chr3:111693678
|
T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(12): Show | 16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-14248T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693678 | ||||||
chr3:111693691
|
C | T | 10 | a0001c0001t0003g0032a0001c0001t0003g0249a0001c0001t0003g0251others(7): Show | 11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-14235C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693691 | ||||||
chr3:111693942
|
A | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(246): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.164-13984A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111693942 | ||||||
chr3:111694011
|
G | A | 1 | a0001c0001t0004g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.164-13915G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694011 | ||||||
chr3:111694085
|
A | G | 1 | a0001c0001t0006g0179 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.164-13841A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694085 | ||||||
chr3:111694130
|
C | A | 1 | a0001c0001t0006g0041 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.164-13796C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694130 | ||||||
chr3:111694168
|
C | G | 15 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(12): Show | 16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-13758C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694168 | ||||||
chr3:111694241
|
G | A | 1 | a0001c0001t0031g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-13685G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694241 | ||||||
chr3:111694423
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0049others(3): Show | 6 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-13503G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694423 | ||||||
chr3:111694471
|
C | CT | 20 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0084others(17): Show | 20 | HG00738.hp2 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.164-13442dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111694471 | |||||
chr3:111694471
|
CT | C | 11 | a0001c0001t0002g0181a0001c0001t0003g0017a0001c0001t0004g0002others(8): Show | 16 | HG00099.hp2 HG00280.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-13442delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111694471 | |||||
chr3:111694832
|
T | G | 1 | a0001c0001t0024g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-13094T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111694832 | ||||||
chr3:111695073
|
C | T | 8 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0049others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-12853C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695073 | ||||||
chr3:111695090
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.164-12836A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695090 | ||||||
chr3:111695142
|
AT | A | 17 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0121others(14): Show | 18 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-12777delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111695142 | |||||
chr3:111695160
|
T | TA | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(209): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.164-12745dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111695160 | |||||
chr3:111695160
|
T | TAA | 16 | a0001c0001t0001g0060a0001c0001t0001g0086a0001c0001t0001g0092others(13): Show | 17 | HG01981.hp1 HG02080.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.164-12746_164-1274 others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111695160 | |||||
chr3:111695486
|
T | G | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-12440T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695486 | ||||||
chr3:111695524
|
C | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-12402C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695524 | ||||||
chr3:111695559
|
A | G | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-12367A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695559 | ||||||
chr3:111695613
|
C | A | 4 | a0001c0001t0003g0028a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 5 | HG02055.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-12313C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695613 | ||||||
chr3:111695651
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.164-12275A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695651 | ||||||
chr3:111695726
|
A | G | 15 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0248others(12): Show | 16 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.164-12200A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695726 | ||||||
chr3:111695737
|
G | C | 15 | a0001c0001t0003g0032a0001c0001t0003g0249a0001c0001t0003g0251others(12): Show | 18 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-12189G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695737 | ||||||
chr3:111695765
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(262): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.164-12161G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695765 | ||||||
chr3:111695996
|
T | C | 1 | a0001c0001t0003g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164-11930T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111695996 | ||||||
chr3:111696092
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0028others(10): Show | 14 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.164-11834A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696092 | ||||||
chr3:111696108
|
G | A | 2 | a0001c0001t0004g0024a0001c0001t0004g0141 | 3 | HG01168.hp1 HG01433.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.164-11818G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696108 | ||||||
chr3:111696126
|
G | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(265): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.164-11800G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696126 | ||||||
chr3:111696200
|
G | T | 7 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0049others(4): Show | 7 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-11726G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696200 | ||||||
chr3:111696252
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-11674G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696252 | ||||||
chr3:111696336
|
T | G | 3 | a0001c0001t0001g0144a0001c0001t0002g0173a0001c0001t0006g0143 | 3 | HG00621.hp2 NA18953.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.164-11590T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696336 | ||||||
chr3:111696379
|
G | T | 1 | a0001c0001t0050g0210 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.164-11547G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696379 | ||||||
chr3:111696464
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.164-11462A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696464 | ||||||
chr3:111696600
|
A | G | 9 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0049others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-11326A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696600 | ||||||
chr3:111696632
|
T | C | 1 | a0001c0001t0010g0066 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.164-11294T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696632 | ||||||
chr3:111696749
|
C | A | 4 | a0001c0001t0003g0118a0001c0001t0009g0111a0001c0001t0009g0227others(1): Show | 4 | HG02698.hp1 HG04115.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-11177C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696749 | ||||||
chr3:111696749
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.164-11177C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111696749 | ||||||
chr3:111697208
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.164-10718G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697208 | ||||||
chr3:111697293
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0248a0001c0001t0003g0049others(3): Show | 6 | HG00738.hp2 HG01109.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-10633G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697293 | ||||||
chr3:111697307
|
A | T | 10 | a0001c0001t0003g0032a0001c0001t0003g0249a0001c0001t0003g0251others(7): Show | 11 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-10619A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697307 | ||||||
chr3:111697406
|
A | G | 1 | a0001c0001t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.164-10520A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697406 | ||||||
chr3:111697415
|
G | C | 5 | a0001c0001t0004g0014a0001c0001t0004g0263a0001c0001t0004g0264others(2): Show | 7 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-10511G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697415 | ||||||
chr3:111697463
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(109): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.164-10463A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697463 | ||||||
chr3:111697604
|
A | C | 17 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0121others(14): Show | 18 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-10322A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697604 | ||||||
chr3:111697841
|
C | T | 2 | a0001c0001t0030g0265a0001c0001t0033g0266 | 2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.164-10085C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111697841 | ||||||
chr3:111697843
|
G | GTATT | 265 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(262): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.164-10077_164-1007 others(8): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111697843 | |||||
chr3:111698867
|
C | G | 1 | a0001c0001t0031g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-9059C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698867 | ||||||
chr3:111698916
|
A | G | 4 | a0001c0001t0004g0022a0001c0001t0004g0079a0001c0001t0004g0080others(1): Show | 5 | HG02145.hp1 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-9010A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698916 | ||||||
chr3:111698942
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.164-8984T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698942 | ||||||
chr3:111698946
|
A | G | 1 | a0001c0001t0031g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-8980A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111698946 | ||||||
chr3:111699258
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.164-8668T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699258 | ||||||
chr3:111699282
|
G | A | 1 | a0001c0001t0024g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-8644G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699282 | ||||||
chr3:111699337
|
T | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(268): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.164-8589T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699337 | ||||||
chr3:111699356
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.164-8570G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699356 | ||||||
chr3:111699524
|
A | G | 1 | a0001c0001t0025g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164-8402A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699524 | ||||||
chr3:111699678
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.164-8248G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699678 | ||||||
chr3:111699720
|
A | T | 1 | a0001c0001t0003g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.164-8206A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699720 | ||||||
chr3:111699777
|
A | G | 1 | a0001c0001t0004g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-8149A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699777 | ||||||
chr3:111699891
|
T | C | 1 | a0001c0001t0005g0235 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.164-8035T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111699891 | ||||||
chr3:111700126
|
G | A | 1 | a0001c0001t0038g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-7800G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700126 | ||||||
chr3:111700143
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-7783T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700143 | ||||||
chr3:111700154
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(92): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.164-7772C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700154 | ||||||
chr3:111700213
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(260): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.164-7713A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700213 | ||||||
chr3:111700288
|
G | A | 1 | a0001c0001t0032g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.164-7638G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700288 | ||||||
chr3:111700483
|
T | C | 1 | a0001c0001t0002g0190 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.164-7443T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700483 | ||||||
chr3:111700610
|
GA | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(90): Show | 110 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.164-7306delA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111700610 | |||||
chr3:111700639
|
G | T | 53 | a0001c0001t0003g0013a0001c0001t0003g0032a0001c0001t0003g0033others(50): Show | 68 | HG00408.hp1 HG00639.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.164-7287G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700639 | ||||||
chr3:111700668
|
G | A | 14 | a0001c0001t0001g0147a0001c0001t0002g0003a0001c0001t0002g0007others(11): Show | 21 | HG00438.hp2 HG00621.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.164-7258G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700668 | ||||||
chr3:111700697
|
A | C | 1 | a0001c0001t0046g0157 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.164-7229A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700697 | ||||||
chr3:111700845
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.164-7081C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700845 | ||||||
chr3:111700851
|
G | T | 2 | a0001c0001t0013g0208a0001c0001t0013g0209 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.164-7075G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700851 | ||||||
chr3:111700883
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0138a0001c0001t0001g0145others(4): Show | 8 | HG01071.hp1 HG01109.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-7043C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700883 | ||||||
chr3:111700970
|
G | A | 2 | a0001c0001t0007g0123a0001c0001t0007g0214 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.164-6956G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111700970 | ||||||
chr3:111701531
|
C | T | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-6395C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701531 | ||||||
chr3:111701564
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0061a0001c0001t0002g0081 | 4 | NA18952.hp2 NA18970.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-6362C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701564 | ||||||
chr3:111701671
|
T | C | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.164-6255T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701671 | ||||||
chr3:111701714
|
A | G | 47 | a0001c0001t0002g0151a0001c0001t0003g0017a0001c0001t0003g0028others(44): Show | 49 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.164-6212A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701714 | ||||||
chr3:111701972
|
T | C | 3 | a0001c0001t0002g0063a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG02015.hp1 HG02080.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.164-5954T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111701972 | ||||||
chr3:111702486
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.164-5440T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702486 | ||||||
chr3:111702567
|
C | T | 6 | a0001c0001t0003g0013a0001c0001t0003g0212a0001c0001t0003g0216others(3): Show | 8 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-5359C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702567 | ||||||
chr3:111702651
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164-5275C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702651 | ||||||
chr3:111702663
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(260): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.164-5263T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702663 | ||||||
chr3:111702840
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.164-5086A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702840 | ||||||
chr3:111702858
|
C | T | 41 | a0001c0001t0003g0028a0001c0001t0003g0043a0001c0001t0003g0047others(38): Show | 42 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.164-5068C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702858 | ||||||
chr3:111702958
|
T | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(220): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.164-4968T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111702958 | ||||||
chr3:111703047
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(219): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.164-4879T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703047 | ||||||
chr3:111703216
|
G | A | 3 | a0001c0001t0003g0137a0001c0001t0003g0153a0001c0001t0003g0154 | 3 | HG00741.hp1 HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.164-4710G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703216 | ||||||
chr3:111703516
|
A | G | 1 | a0001c0001t0004g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.164-4410A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703516 | ||||||
chr3:111703855
|
C | A | 1 | a0001c0001t0009g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.164-4071C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111703855 | ||||||
chr3:111704189
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.164-3737G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704189 | ||||||
chr3:111704202
|
G | GGGGTAGT others(15): Show |
3 | a0001c0001t0003g0013a0001c0001t0003g0212a0001c0001t0004g0213 | 5 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-3723_164-3702d others(24): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111704202 | |||||
chr3:111704246
|
A | G | 1 | a0001c0001t0004g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.164-3680A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704246 | ||||||
chr3:111704282
|
G | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(244): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.164-3644G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704282 | ||||||
chr3:111704337
|
C | T | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.164-3589C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704337 | ||||||
chr3:111704495
|
A | C | 50 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0043others(47): Show | 52 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.164-3431A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704495 | ||||||
chr3:111704566
|
T | G | 47 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0043others(44): Show | 49 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.164-3360T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704566 | ||||||
chr3:111704783
|
A | G | 34 | a0001c0001t0003g0013a0001c0001t0003g0032a0001c0001t0003g0033others(31): Show | 49 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.164-3143A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704783 | ||||||
chr3:111704817
|
A | AT | 51 | a0001c0001t0002g0069a0001c0001t0003g0017a0001c0001t0003g0028others(48): Show | 53 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.164-3094dupT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111704817 | |||||
chr3:111704922
|
C | A | 1 | a0001c0001t0003g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.164-3004C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704922 | ||||||
chr3:111704936
|
C | T | 4 | a0001c0001t0003g0047a0001c0001t0003g0049a0001c0001t0003g0125others(1): Show | 4 | HG01192.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-2990C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111704936 | ||||||
chr3:111705055
|
G | T | 1 | a0003c0004t0041g0072 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.164-2871G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705055 | ||||||
chr3:111705064
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.164-2862G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705064 | ||||||
chr3:111705066
|
C | T | 34 | a0001c0001t0003g0013a0001c0001t0003g0032a0001c0001t0003g0033others(31): Show | 49 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.164-2860C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705066 | ||||||
chr3:111705257
|
T | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0049 | 2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.164-2669T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705257 | ||||||
chr3:111705318
|
C | T | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-2608C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705318 | ||||||
chr3:111705377
|
G | T | 1 | a0001c0001t0015g0050 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.164-2549G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705377 | ||||||
chr3:111705481
|
G | T | 1 | a0001c0001t0001g0130 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.164-2445G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705481 | ||||||
chr3:111705682
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(183): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.164-2244G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111705682 | ||||||
chr3:111706050
|
G | T | 1 | a0001c0001t0002g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.164-1876G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706050 | ||||||
chr3:111706185
|
A | G | 1 | a0001c0001t0032g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.164-1741A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706185 | ||||||
chr3:111706530
|
A | G | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164-1396A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706530 | ||||||
chr3:111706558
|
G | T | 1 | a0001c0001t0002g0181 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.164-1368G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706558 | ||||||
chr3:111706754
|
C | A | 1 | a0001c0001t0001g0026 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.164-1172C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706754 | ||||||
chr3:111706754
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.164-1172C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706754 | ||||||
chr3:111706812
|
C | CA | 5 | a0001c0001t0001g0027a0001c0001t0001g0128a0001c0001t0001g0160others(2): Show | 6 | HG02300.hp1 NA18963.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-1099dupA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | |||||
chr3:111706812
|
C | CAAA | 6 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(3): Show | 6 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-1101_164-1099d others(5): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | |||||
chr3:111706812
|
CA | C | 117 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(114): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.164-1099delA | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | |||||
chr3:111706812
|
CAA | C | 7 | a0001c0001t0002g0081a0001c0001t0003g0259a0001c0001t0004g0038others(4): Show | 7 | HG01358.hp2 HG02602.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1100_164-1099d others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 111706812 | |||||
chr3:111706918
|
C | G | 1 | a0001c0001t0001g0078 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.164-1008C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111706918 | ||||||
chr3:111707141
|
G | A | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-785G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707141 | ||||||
chr3:111707445
|
A | G | 1 | a0001c0001t0004g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-481A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707445 | ||||||
chr3:111707479
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.164-447A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707479 | ||||||
chr3:111707819
|
A | G | 9 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(6): Show | 9 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-107A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707819 | ||||||
chr3:111707843
|
T | G | 25 | a0001c0001t0003g0028a0001c0001t0003g0043a0001c0001t0003g0095others(22): Show | 26 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.164-83T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707843 | ||||||
chr3:111707860
|
A | T | 4 | a0001c0001t0008g0031a0001c0001t0008g0052a0001c0001t0008g0053others(1): Show | 5 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-66A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 1/3 | chr3 | 111707860 | ||||||
chr3:111708447
|
G | C | 1 | a0001c0001t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.624+61G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708447 | ||||||
chr3:111708512
|
T | A | 1 | a0001c0001t0002g0069 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.624+126T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708512 | ||||||
chr3:111708523
|
C | T | 1 | a0005c0006t0018g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.624+137C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708523 | ||||||
chr3:111708583
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.624+197T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708583 | ||||||
chr3:111708608
|
G | A | 56 | a0001c0001t0001g0149a0001c0001t0002g0003a0001c0001t0002g0004others(53): Show | 72 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.624+222G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708608 | ||||||
chr3:111708876
|
G | A | 7 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(4): Show | 7 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+490G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708876 | ||||||
chr3:111708988
|
C | T | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.624+602C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111708988 | ||||||
chr3:111708994
|
G | GGAAGAGG others(3): Show |
16 | a0001c0001t0003g0196a0001c0001t0003g0216a0001c0001t0003g0217others(13): Show | 16 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.624+610_624+619dup others(10): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 111708994 | |||||
chr3:111709090
|
TG | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(96): Show | 119 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.624+706delG | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 111709090 | |||||
chr3:111709091
|
G | GA | 53 | a0001c0001t0001g0149a0001c0001t0002g0003a0001c0001t0002g0004others(50): Show | 69 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.624+705_624+706ins others(1): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709091 | ||||||
chr3:111709091
|
GGA | G | 4 | a0001c0001t0001g0128a0001c0001t0010g0077a0001c0001t0012g0197others(1): Show | 4 | HG02559.hp1 HG02818.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+706_624+707del others(2): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709091 | ||||||
chr3:111709092
|
G | A | 144 | a0001c0001t0001g0149a0001c0001t0002g0003a0001c0001t0002g0004others(141): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.624+706G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709092 | ||||||
chr3:111709290
|
A | T | 1 | a0001c0001t0003g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.624+904A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709290 | ||||||
chr3:111709467
|
T | TAC | 83 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0028others(80): Show | 100 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.624+1096_624+1097d others(4): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 111709467 | |||||
chr3:111709531
|
C | T | 1 | a0001c0001t0004g0030 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.624+1145C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709531 | ||||||
chr3:111709620
|
A | G | 1 | a0001c0001t0015g0050 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.624+1234A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709620 | ||||||
chr3:111709680
|
G | C | 91 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0028others(88): Show | 108 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.624+1294G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709680 | ||||||
chr3:111709733
|
A | G | 7 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(4): Show | 7 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+1347A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709733 | ||||||
chr3:111709919
|
A | G | 145 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(142): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.624+1533A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709919 | ||||||
chr3:111709944
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0206 | 3 | HG02735.hp1 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.624+1558G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111709944 | ||||||
chr3:111710021
|
C | T | 1 | a0001c0001t0039g0222 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.624+1635C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710021 | ||||||
chr3:111710064
|
C | T | 6 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+1678C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710064 | ||||||
chr3:111710098
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.624+1712G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710098 | ||||||
chr3:111710163
|
C | T | 2 | a0001c0003t0011g0182a0001c0003t0011g0183 | 2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.624+1777C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710163 | ||||||
chr3:111710168
|
G | A | 1 | a0001c0001t0015g0050 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.624+1782G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710168 | ||||||
chr3:111710514
|
C | T | 2 | a0001c0003t0011g0182a0001c0003t0011g0183 | 2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.624+2128C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710514 | ||||||
chr3:111710570
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.624+2184C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710570 | ||||||
chr3:111710606
|
C | T | 3 | a0001c0001t0004g0014a0001c0001t0004g0263a0001c0001t0004g0264 | 5 | HG02809.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+2220C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710606 | ||||||
chr3:111710685
|
G | A | 52 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0043others(49): Show | 54 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.624+2299G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710685 | ||||||
chr3:111710746
|
G | C | 2 | a0001c0001t0003g0256a0001c0001t0003g0258 | 2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.624+2360G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710746 | ||||||
chr3:111710835
|
T | G | 3 | a0001c0001t0014g0037a0001c0001t0036g0100a0005c0006t0018g0120 | 3 | HG02717.hp1 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.624+2449T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111710835 | ||||||
chr3:111711009
|
A | G | 34 | a0001c0001t0003g0013a0001c0001t0003g0032a0001c0001t0003g0033others(31): Show | 49 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.624+2623A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711009 | ||||||
chr3:111711220
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(244): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.625-2667G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711220 | ||||||
chr3:111711277
|
G | A | 5 | a0001c0001t0003g0047a0001c0001t0003g0049a0001c0001t0003g0125others(2): Show | 5 | HG01192.hp1 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-2610G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711277 | ||||||
chr3:111711400
|
G | A | 1 | a0001c0001t0006g0188 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.625-2487G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711400 | ||||||
chr3:111711532
|
A | T | 2 | a0001c0001t0010g0076a0001c0001t0010g0077 | 2 | NA19002.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.625-2355A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711532 | ||||||
chr3:111711788
|
A | T | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.625-2099A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711788 | ||||||
chr3:111711874
|
A | G | 2 | a0001c0001t0003g0028a0001c0001t0003g0195 | 3 | HG02055.hp2 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625-2013A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111711874 | ||||||
chr3:111712122
|
G | C | 53 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(50): Show | 69 | HG00140.hp1 HG00438.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.625-1765G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712122 | ||||||
chr3:111712218
|
C | A | 1 | a0001c0001t0002g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.625-1669C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712218 | ||||||
chr3:111712350
|
A | G | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-1537A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712350 | ||||||
chr3:111712399
|
C | A | 1 | a0001c0001t0004g0114 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.625-1488C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712399 | ||||||
chr3:111712432
|
CT | C | 6 | a0001c0001t0008g0031a0001c0001t0008g0052a0001c0001t0008g0053others(3): Show | 7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-1454delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712432 | ||||||
chr3:111712475
|
C | T | 1 | a0001c0001t0032g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.625-1412C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712475 | ||||||
chr3:111712505
|
C | T | 46 | a0001c0001t0002g0064a0001c0001t0003g0028a0001c0001t0003g0043others(43): Show | 47 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.625-1382C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712505 | ||||||
chr3:111712577
|
G | A | 1 | a0001c0001t0039g0222 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.625-1310G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712577 | ||||||
chr3:111712601
|
C | G | 1 | a0001c0001t0032g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.625-1286C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712601 | ||||||
chr3:111712630
|
A | G | 1 | a0001c0001t0014g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-1257A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712630 | ||||||
chr3:111712646
|
C | A | 6 | a0001c0001t0008g0031a0001c0001t0008g0052a0001c0001t0008g0053others(3): Show | 7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-1241C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712646 | ||||||
chr3:111712744
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(85): Show | 105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.625-1143G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712744 | ||||||
chr3:111712764
|
C | T | 1 | a0001c0001t0004g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.625-1123C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712764 | ||||||
chr3:111712772
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.625-1115T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712772 | ||||||
chr3:111712971
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(84): Show | 104 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.625-916G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111712971 | ||||||
chr3:111713042
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.625-845G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713042 | ||||||
chr3:111713053
|
C | T | 25 | a0001c0001t0003g0028a0001c0001t0003g0043a0001c0001t0003g0095others(22): Show | 26 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.625-834C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713053 | ||||||
chr3:111713355
|
A | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0177others(1): Show | 4 | NA18964.hp2 NA18988.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-532A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713355 | ||||||
chr3:111713391
|
G | A | 48 | a0001c0001t0003g0017a0001c0001t0003g0028a0001c0001t0003g0043others(45): Show | 50 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.625-496G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713391 | ||||||
chr3:111713467
|
T | A | 2 | a0001c0003t0011g0182a0001c0003t0011g0183 | 2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.625-420T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713467 | ||||||
chr3:111713652
|
A | G | 4 | a0001c0001t0014g0037a0001c0001t0014g0110a0001c0001t0024g0194others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-235A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713652 | ||||||
chr3:111713816
|
G | A | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-71G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713816 | ||||||
chr3:111713824
|
C | T | 5 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-63C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 2/3 | chr3 | 111713824 | ||||||
chr3:111714201
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.866+73C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714201 | ||||||
chr3:111714205
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.866+77G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714205 | ||||||
chr3:111714449
|
G | A | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.866+321G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714449 | ||||||
chr3:111714481
|
T | G | 1 | a0001c0001t0006g0188 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.866+353T>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714481 | ||||||
chr3:111714579
|
C | T | 52 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(49): Show | 68 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.866+451C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714579 | ||||||
chr3:111714647
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(245): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.866+519T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714647 | ||||||
chr3:111714775
|
C | T | 1 | a0001c0001t0038g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.866+647C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714775 | ||||||
chr3:111714823
|
C | CAT | 6 | a0001c0001t0008g0031a0001c0001t0008g0052a0001c0001t0008g0053others(3): Show | 7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.866+696_866+697dup others(2): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111714823 | |||||
chr3:111714968
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(244): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.866+840C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111714968 | ||||||
chr3:111715047
|
A | G | 1 | a0002c0002t0002g0010 | 3 | NA18945.hp1 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.866+919A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715047 | ||||||
chr3:111715209
|
T | C | 1 | a0001c0001t0003g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.866+1081T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715209 | ||||||
chr3:111715269
|
C | G | 33 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0259others(30): Show | 46 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+1141C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715269 | ||||||
chr3:111715286
|
T | C | 1 | a0001c0001t0006g0042 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.866+1158T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715286 | ||||||
chr3:111715374
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(268): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.866+1246C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715374 | ||||||
chr3:111715396
|
A | G | 1 | a0001c0001t0037g0175 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.866+1268A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715396 | ||||||
chr3:111715459
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.866+1331G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715459 | ||||||
chr3:111715597
|
G | A | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+1469G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715597 | ||||||
chr3:111715960
|
T | C | 2 | a0001c0001t0006g0046a0001c0001t0038g0250 | 2 | HG01081.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.866+1832T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715960 | ||||||
chr3:111715964
|
G | C | 1 | a0001c0001t0040g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.866+1836G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111715964 | ||||||
chr3:111716022
|
G | A | 1 | a0001c0001t0030g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.866+1894G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716022 | ||||||
chr3:111716023
|
C | T | 1 | a0001c0001t0034g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.866+1895C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716023 | ||||||
chr3:111716141
|
A | T | 2 | a0001c0003t0011g0182a0001c0003t0011g0183 | 2 | HG00140.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.866+2013A>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716141 | ||||||
chr3:111716148
|
C | T | 4 | a0001c0001t0014g0037a0001c0001t0014g0110a0001c0001t0036g0100others(1): Show | 4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+2020C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716148 | ||||||
chr3:111716190
|
G | A | 1 | a0002c0002t0042g0070 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.866+2062G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716190 | ||||||
chr3:111716271
|
C | G | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.866+2143C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716271 | ||||||
chr3:111716276
|
G | A | 33 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0259others(30): Show | 46 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2148G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716276 | ||||||
chr3:111716571
|
T | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(53): Show | 72 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.866+2443T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716571 | ||||||
chr3:111716629
|
C | G | 2 | a0001c0001t0017g0106a0001c0001t0032g0201 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.866+2501C>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716629 | ||||||
chr3:111716635
|
G | T | 1 | a0001c0001t0019g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.866+2507G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716635 | ||||||
chr3:111716700
|
A | C | 33 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0259others(30): Show | 46 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2572A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716700 | ||||||
chr3:111716738
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(262): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.866+2610C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716738 | ||||||
chr3:111716956
|
C | T | 2 | a0001c0001t0014g0037a0001c0001t0014g0110 | 2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.866+2828C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716956 | ||||||
chr3:111716969
|
G | A | 1 | a0001c0001t0031g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.866+2841G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716969 | ||||||
chr3:111716993
|
C | T | 43 | a0001c0001t0003g0013a0001c0001t0003g0028a0001c0001t0003g0043others(40): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2865C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111716993 | ||||||
chr3:111717110
|
C | T | 43 | a0001c0001t0003g0013a0001c0001t0003g0028a0001c0001t0003g0043others(40): Show | 46 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.866+2982C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717110 | ||||||
chr3:111717212
|
T | C | 1 | a0001c0001t0006g0232 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.866+3084T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717212 | ||||||
chr3:111717323
|
G | T | 4 | a0001c0001t0014g0037a0001c0001t0014g0110a0001c0001t0036g0100others(1): Show | 4 | HG02258.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+3195G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717323 | ||||||
chr3:111717401
|
C | T | 1 | a0001c0001t0015g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.866+3273C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717401 | ||||||
chr3:111717507
|
G | T | 1 | a0001c0001t0038g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.867-3216G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717507 | ||||||
chr3:111717772
|
A | C | 3 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199 | 3 | HG02559.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.867-2951A>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717772 | ||||||
chr3:111717793
|
A | G | 1 | a0001c0001t0038g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.867-2930A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111717793 | ||||||
chr3:111717990
|
CT | C | 94 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(91): Show | 123 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.867-2722delT | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111717990 | |||||
chr3:111718231
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867-2492G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718231 | ||||||
chr3:111718281
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.867-2442G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718281 | ||||||
chr3:111718325
|
C | A | 2 | a0001c0001t0014g0037a0001c0001t0014g0110 | 2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.867-2398C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718325 | ||||||
chr3:111718329
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(261): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.867-2394G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718329 | ||||||
chr3:111718357
|
C | A | 1 | a0001c0001t0001g0116 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.867-2366C>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718357 | ||||||
chr3:111718397
|
G | A | 7 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0003g0101others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.867-2326G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718397 | ||||||
chr3:111718403
|
T | C | 1 | a0001c0001t0038g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.867-2320T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718403 | ||||||
chr3:111718443
|
G | C | 1 | a0001c0001t0002g0090 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.867-2280G>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718443 | ||||||
chr3:111718449
|
A | G | 1 | a0001c0001t0039g0222 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.867-2274A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718449 | ||||||
chr3:111718491
|
T | TGATA | 17 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0078others(14): Show | 17 | HG00140.hp2 HG01106.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.867-2192_867-2189d others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718491 | |||||
chr3:111718491
|
T | TGATAGAT others(1): Show |
6 | a0001c0001t0001g0133a0001c0001t0001g0177a0001c0001t0001g0220others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-2196_867-2189d others(10): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718491 | |||||
chr3:111718491
|
TGATA | T | 5 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0012g0197others(2): Show | 5 | HG01109.hp2 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.867-2192_867-2189d others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718491 | |||||
chr3:111718519
|
AGATAGAT others(9): Show |
A | 2 | a0001c0001t0003g0154a0001c0001t0015g0260 | 2 | HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.867-2200_867-2185d others(18): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718519 | |||||
chr3:111718523
|
AGATAGAT others(5): Show |
A | 10 | a0001c0001t0002g0003a0001c0001t0003g0028a0001c0001t0003g0137others(7): Show | 15 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.867-2196_867-2185d others(14): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718523 | |||||
chr3:111718523
|
AGATAGAT others(9): Show |
A | 1 | a0001c0001t0039g0222 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.867-2196_867-2181d others(18): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718523 | |||||
chr3:111718527
|
AGATAGAT others(1): Show |
A | 46 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0136others(43): Show | 57 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.867-2192_867-2185d others(10): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718527 | |||||
chr3:111718529
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.867-2194A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718529 | ||||||
chr3:111718531
|
AGATT | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0059others(62): Show | 79 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.867-2183_867-2180d others(6): Show |
PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 111718531 | |||||
chr3:111718535
|
T | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(127): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.867-2188T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718535 | ||||||
chr3:111718539
|
T | A | 2 | a0001c0001t0002g0093a0001c0001t0003g0108 | 2 | HG04199.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.867-2184T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718539 | ||||||
chr3:111718606
|
G | A | 2 | a0001c0001t0024g0194a0001c0001t0030g0265 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.867-2117G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718606 | ||||||
chr3:111718842
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.867-1881A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718842 | ||||||
chr3:111718871
|
T | A | 6 | a0001c0001t0008g0031a0001c0001t0008g0052a0001c0001t0008g0053others(3): Show | 7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.867-1852T>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718871 | ||||||
chr3:111718907
|
C | T | 3 | a0001c0001t0011g0244a0001c0003t0011g0182a0001c0003t0011g0183 | 3 | HG00140.hp2 HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.867-1816C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111718907 | ||||||
chr3:111719030
|
C | T | 1 | a0001c0001t0022g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.867-1693C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719030 | ||||||
chr3:111719031
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0245 | 2 | HG01256.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.867-1692G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719031 | ||||||
chr3:111719250
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(261): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.867-1473T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719250 | ||||||
chr3:111719268
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.867-1455C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719268 | ||||||
chr3:111719273
|
C | T | 4 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1450C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719273 | ||||||
chr3:111719524
|
G | T | 1 | a0001c0001t0032g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.867-1199G>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719524 | ||||||
chr3:111719572
|
C | T | 3 | a0001c0001t0007g0023a0001c0001t0007g0112a0001c0001t0007g0119 | 4 | HG01256.hp1 HG01258.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-1151C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719572 | ||||||
chr3:111719596
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0006others(49): Show | 68 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.867-1127G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719596 | ||||||
chr3:111719797
|
T | C | 1 | a0001c0001t0050g0210 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.867-926T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719797 | ||||||
chr3:111719887
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(261): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.867-836C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719887 | ||||||
chr3:111719907
|
A | G | 1 | a0001c0001t0006g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.867-816A>G | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111719907 | ||||||
chr3:111720150
|
G | A | 7 | a0001c0001t0008g0031a0001c0001t0008g0052a0001c0001t0008g0053others(4): Show | 8 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.867-573G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720150 | ||||||
chr3:111720278
|
G | A | 10 | a0001c0001t0012g0197a0001c0001t0012g0198a0001c0001t0012g0199others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.867-445G>A | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720278 | ||||||
chr3:111720291
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(261): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.867-432T>C | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720291 | ||||||
chr3:111720311
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(164): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.867-412C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720311 | ||||||
chr3:111720696
|
C | T | 18 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0196others(15): Show | 20 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.867-27C>T | PLCXD2 | ENSG00000240891.8 | transcript | ENST00000636933.2 | protein_coding | 3/3 | chr3 | 111720696 |