geneid | 23207 |
---|---|
ensemblid | ENSG00000116786.13 |
hgncid | 29131 |
symbol | PLEKHM2 |
name | pleckstrin homology and RUN domain containing M2 |
refseq_nuc | NM_015164.4 |
refseq_prot | NP_055979.2 |
ensembl_nuc | ENST00000375799.8 |
ensembl_prot | ENSP00000364956.3 |
mane_status | MANE Select |
chr | chr1 |
start | 15684320 |
end | 15734769 |
strand | + |
ver | v1.2 |
region | chr1:15684320-15734769 |
region5000 | chr1:15679320-15739769 |
regionname0 | PLEKHM2_chr1_15684320_15734769 |
regionname5000 | PLEKHM2_chr1_15679320_15739769 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1019 | 209 | 20 | 48 | 98 | 12 | 29 | 74 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002 | 0/0 | 1019 | 114 | 65 | 21 | 13 | 5 | 10 | 11 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0003 | 0/0 | 1019 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0004 | 0/0 | 1019 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0005 | 0/0 | 1019 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0006 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0007 | 0/0 | 1019 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0008 | 0/0 | 1019 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0009 | 0/0 | 1019 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0010 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0011 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0012 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0013 | 0/0 | 1019 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0014 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3060 | 187 | 16 | 47 | 92 | 10 | 20 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0002 | 0/0 | 3060 | 59 | 36 | 10 | 5 | 3 | 5 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0003 | 0/0 | 3060 | 16 | 11 | 5 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0004 | 0/0 | 3060 | 14 | 4 | 1 | 3 | 2 | 4 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0005 | 0/0 | 3060 | 13 | 2 | 2 | 8 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0006 | 0/0 | 3060 | 12 | 12 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0007 | 0/0 | 3060 | 6 | 2 | 1 | 0 | 1 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0008 | 0/0 | 3060 | 4 | 0 | 0 | 0 | 0 | 4 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0009 | 0/0 | 3060 | 3 | 0 | 0 | 0 | 1 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0010 | 0/0 | 3060 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0011 | 0/0 | 3060 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0012 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0013 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0014 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0015 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0016 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0017 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0018 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0019 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0020 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0021 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0022 | 0/0 | 3060 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0023 | 0/0 | 3060 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0024 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0025 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0026 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0027 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
c0028 | 0/0 | 3060 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1078 | 105 | 8 | 26 | 54 | 4 | 12 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0002 | 1/0 | 1075 | 102 | 15 | 23 | 37 | 8 | 18 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0003 | 0/0 | 1078 | 54 | 25 | 10 | 5 | 5 | 9 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0004 | 0/0 | 1078 | 20 | 16 | 4 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0005 | 0/0 | 1075 | 10 | 2 | 3 | 3 | 0 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0006 | 0/0 | 1078 | 9 | 8 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0007 | 0/0 | 1075 | 7 | 0 | 0 | 7 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0008 | 0/0 | 1078 | 7 | 6 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0009 | 0/0 | 1075 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0010 | 0/0 | 1078 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0011 | 0/0 | 1078 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0012 | 0/0 | 1078 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0013 | 0/0 | 1090 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0014 | 0/0 | 1078 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0015 | 0/0 | 1078 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0016 | 0/0 | 1078 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0017 | 0/0 | 1075 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0018 | 0/0 | 1075 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0019 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
t0020 | 0/0 | 1078 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3060 | 187 | 16 | 47 | 92 | 10 | 20 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0004 | 0/0 | 3060 | 14 | 4 | 1 | 3 | 2 | 4 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0008 | 0/0 | 3060 | 4 | 0 | 0 | 0 | 0 | 4 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0011 | 0/0 | 3060 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0024 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0028 | 0/0 | 3060 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002 | 0/0 | 3060 | 59 | 36 | 10 | 5 | 3 | 5 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003 | 0/0 | 3060 | 16 | 11 | 5 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0005 | 0/0 | 3060 | 13 | 2 | 2 | 8 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0006 | 0/0 | 3060 | 12 | 12 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0007 | 0/0 | 3060 | 6 | 2 | 1 | 0 | 1 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0009 | 0/0 | 3060 | 3 | 0 | 0 | 0 | 1 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0010 | 0/0 | 3060 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0012 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0014 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0003c0015 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0003c0019 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0004c0027 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0005c0021 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0006c0026 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0007c0025 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0008c0023 | 0/0 | 3060 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0009c0022 | 0/0 | 3060 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0010c0020 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0011c0013 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0012c0018 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0013c0017 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0014c0016 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4137 | 79 | 1 | 23 | 44 | 3 | 7 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0001t0002 | 1/0 | 4134 | 93 | 15 | 23 | 35 | 7 | 12 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0001t0005 | 0/0 | 4134 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0001t0007 | 0/0 | 4134 | 7 | 0 | 0 | 7 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0001t0009 | 0/0 | 4134 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0001t0015 | 0/0 | 4137 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0001t0016 | 0/0 | 4137 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0001t0017 | 0/0 | 4134 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0004t0003 | 0/0 | 4137 | 5 | 2 | 0 | 0 | 1 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0004t0005 | 0/0 | 4134 | 8 | 2 | 1 | 3 | 0 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0004t0014 | 0/0 | 4137 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0008t0002 | 0/0 | 4134 | 4 | 0 | 0 | 0 | 0 | 4 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0011t0001 | 0/0 | 4137 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0024t0002 | 0/0 | 4134 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0001c0028t0002 | 0/0 | 4134 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0003 | 0/0 | 4137 | 37 | 18 | 6 | 5 | 3 | 5 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0004 | 0/0 | 4137 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0006 | 0/0 | 4137 | 8 | 7 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0008 | 0/0 | 4137 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0010 | 0/0 | 4137 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0011 | 0/0 | 4137 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0012 | 0/0 | 4137 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0002t0013 | 0/0 | 4149 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0001 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0003 | 0/0 | 4137 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0004 | 0/0 | 4137 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0006 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0008 | 0/0 | 4137 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0010 | 0/0 | 4137 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0019 | 0/0 | 4119 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0003t0020 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0005t0001 | 0/0 | 4137 | 13 | 2 | 2 | 8 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0006t0004 | 0/0 | 4137 | 12 | 12 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0007t0001 | 0/0 | 4137 | 6 | 2 | 1 | 0 | 1 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0009t0003 | 0/0 | 4137 | 3 | 0 | 0 | 0 | 1 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0010t0003 | 0/0 | 4137 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0012t0003 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0002c0014t0004 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0003c0015t0012 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0003c0019t0004 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0004c0027t0001 | 0/0 | 4137 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0005c0021t0002 | 0/0 | 4134 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0006c0026t0018 | 0/0 | 4134 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0007c0025t0002 | 0/0 | 4134 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0008c0023t0005 | 0/0 | 4134 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0009c0022t0002 | 0/0 | 4134 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0010c0020t0001 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0011c0013t0001 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0012c0018t0008 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0013c0017t0001 | 0/0 | 4137 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
a0014c0016t0008 | 0/0 | 4137 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | copy fasta | chr1 | 15679320 | 15739769 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0007g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0009g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0015g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0016g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0001t0017g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0004t0014g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0008t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0008t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0008t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0008t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0011t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0011t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0024t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0001c0028t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0004g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0010g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0012g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0002t0013g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0008g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0010g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0019g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0003t0020g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0005t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0006t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0007t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0009t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0009t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0009t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0010t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0010t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0012t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0002c0014t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0003c0015t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0003c0019t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0004c0027t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0005c0021t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0006c0026t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0007c0025t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0008c0023t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0009c0022t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0010c0020t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0011c0013t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0012c0018t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0013c0017t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
a0014c0016t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | GBR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | GBR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | GBR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00280 | hp1 | a0001 | c0004 | t0003 | g0196 | EUR | FIN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0251 | EUR | FIN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00323 | hp1 | a0002 | c0007 | t0001 | g0112 | EUR | FIN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | FIN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00544 | hp1 | a0001 | c0028 | t0002 | g0250 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00639 | hp2 | a0002 | c0002 | t0003 | g0075 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00642 | hp2 | a0002 | c0003 | t0008 | g0023 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01069 | hp1 | a0002 | c0007 | t0001 | g0095 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01069 | hp2 | a0002 | c0002 | t0004 | g0043 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01070 | hp2 | a0002 | c0003 | t0004 | g0011 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01071 | hp1 | a0002 | c0003 | t0004 | g0011 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01071 | hp2 | a0002 | c0002 | t0004 | g0010 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01099 | hp1 | a0002 | c0005 | t0001 | g0070 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01099 | hp2 | a0002 | c0003 | t0010 | g0092 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01106 | hp2 | a0002 | c0003 | t0003 | g0087 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01109 | hp1 | a0002 | c0010 | t0003 | g0063 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01109 | hp2 | a0002 | c0002 | t0010 | g0100 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01167 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01243 | hp2 | a0002 | c0002 | t0006 | g0113 | AMR | PUR | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01255 | hp1 | a0002 | c0010 | t0003 | g0008 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01261 | hp2 | a0002 | c0010 | t0003 | g0008 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0077 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01361 | hp1 | a0002 | c0005 | t0001 | g0071 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0074 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01515 | hp1 | a0002 | c0002 | t0003 | g0007 | EUR | IBS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01516 | hp1 | a0002 | c0002 | t0003 | g0009 | EUR | IBS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0009 | EUR | IBS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0134 | EUR | IBS | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01884 | hp1 | a0001 | c0004 | t0005 | g0279 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01884 | hp2 | a0002 | c0002 | t0003 | g0105 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01891 | hp1 | a0002 | c0002 | t0012 | g0026 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01891 | hp2 | a0002 | c0006 | t0004 | g0006 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01952 | hp1 | a0001 | c0004 | t0005 | g0241 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01978 | hp2 | a0008 | c0023 | t0005 | g0233 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0057 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02004 | hp1 | a0002 | c0002 | t0003 | g0065 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02055 | hp1 | a0002 | c0006 | t0004 | g0035 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02055 | hp2 | a0002 | c0002 | t0003 | g0079 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02056 | hp1 | a0002 | c0002 | t0003 | g0081 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02071 | hp1 | a0001 | c0004 | t0005 | g0249 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0260 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02145 | hp2 | a0002 | c0002 | t0003 | g0083 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CDX | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02155 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | CDX | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CDX | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02257 | hp1 | a0003 | c0015 | t0012 | g0025 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02257 | hp2 | a0002 | c0006 | t0004 | g0033 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02258 | hp2 | a0002 | c0003 | t0010 | g0110 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02280 | hp1 | a0002 | c0005 | t0001 | g0069 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02280 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0064 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0062 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02572 | hp1 | a0002 | c0002 | t0006 | g0106 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02572 | hp2 | a0002 | c0006 | t0004 | g0086 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02602 | hp2 | a0013 | c0017 | t0001 | g0090 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02615 | hp1 | a0002 | c0003 | t0004 | g0093 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02615 | hp2 | a0002 | c0002 | t0006 | g0104 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02622 | hp1 | a0002 | c0003 | t0003 | g0120 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02630 | hp2 | a0002 | c0002 | t0004 | g0010 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02647 | hp1 | a0002 | c0014 | t0004 | g0036 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02647 | hp2 | a0002 | c0003 | t0003 | g0119 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02683 | hp1 | a0001 | c0004 | t0003 | g0271 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02698 | hp1 | a0007 | c0025 | t0002 | g0163 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02723 | hp1 | a0002 | c0003 | t0008 | g0022 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02723 | hp2 | a0001 | c0004 | t0003 | g0015 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0007 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02735 | hp2 | a0002 | c0007 | t0001 | g0094 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02809 | hp1 | a0002 | c0006 | t0004 | g0085 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02809 | hp2 | a0002 | c0006 | t0004 | g0091 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02818 | hp1 | a0002 | c0002 | t0006 | g0109 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02818 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02886 | hp1 | a0002 | c0002 | t0006 | g0108 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02886 | hp2 | a0003 | c0019 | t0004 | g0123 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02895 | hp1 | a0002 | c0003 | t0019 | g0115 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02897 | hp2 | a0002 | c0002 | t0006 | g0114 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02922 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02922 | hp2 | a0002 | c0006 | t0004 | g0097 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02965 | hp1 | a0002 | c0012 | t0003 | g0049 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02970 | hp2 | a0002 | c0002 | t0003 | g0051 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02976 | hp1 | a0002 | c0007 | t0001 | g0099 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02976 | hp2 | a0002 | c0002 | t0013 | g0029 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03017 | hp2 | a0002 | c0002 | t0003 | g0080 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0044 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03098 | hp1 | a0002 | c0002 | t0012 | g0027 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03098 | hp2 | a0002 | c0006 | t0004 | g0096 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03130 | hp1 | a0002 | c0002 | t0008 | g0030 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03130 | hp2 | a0002 | c0003 | t0020 | g0024 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03139 | hp1 | a0002 | c0003 | t0003 | g0118 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03139 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03195 | hp2 | a0002 | c0002 | t0008 | g0028 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03209 | hp1 | a0002 | c0002 | t0003 | g0061 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03209 | hp2 | a0002 | c0003 | t0003 | g0116 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0040 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03239 | hp1 | a0001 | c0001 | t0015 | g0003 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0076 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03453 | hp1 | a0002 | c0002 | t0013 | g0031 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03453 | hp2 | a0006 | c0026 | t0018 | g0294 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03486 | hp1 | a0010 | c0020 | t0001 | g0122 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0066 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03490 | hp1 | a0002 | c0009 | t0003 | g0073 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03490 | hp2 | a0004 | c0027 | t0001 | g0297 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03492 | hp2 | a0002 | c0009 | t0003 | g0072 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03516 | hp1 | a0002 | c0006 | t0004 | g0098 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03516 | hp2 | a0002 | c0002 | t0003 | g0041 | AFR | ESN | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0045 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03540 | hp2 | a0002 | c0002 | t0011 | g0004 | AFR | GWD | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03579 | hp1 | a0002 | c0002 | t0011 | g0005 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03669 | hp2 | a0001 | c0004 | t0003 | g0186 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03704 | hp1 | a0002 | c0005 | t0001 | g0060 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03710 | hp2 | a0002 | c0002 | t0003 | g0059 | SAS | PJL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03834 | hp1 | a0002 | c0007 | t0001 | g0089 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03942 | hp1 | a0001 | c0004 | t0005 | g0286 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03942 | hp2 | a0001 | c0008 | t0002 | g0244 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04115 | hp1 | a0002 | c0002 | t0003 | g0067 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04115 | hp2 | a0001 | c0008 | t0002 | g0242 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04184 | hp1 | a0001 | c0008 | t0002 | g0287 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04184 | hp2 | a0001 | c0024 | t0002 | g0220 | SAS | BEB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0291 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG04228 | hp2 | a0001 | c0008 | t0002 | g0285 | SAS | STU | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | CHB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18906 | hp1 | a0002 | c0006 | t0004 | g0034 | AFR | YRI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18906 | hp2 | a0001 | c0004 | t0003 | g0015 | AFR | YRI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18941 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18943 | hp1 | a0001 | c0001 | t0009 | g0255 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18951 | hp2 | a0002 | c0005 | t0001 | g0052 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18954 | hp1 | a0002 | c0005 | t0001 | g0042 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18964 | hp1 | a0002 | c0005 | t0001 | g0055 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18964 | hp2 | a0001 | c0004 | t0005 | g0248 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18968 | hp1 | a0001 | c0004 | t0005 | g0141 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18969 | hp1 | a0002 | c0005 | t0001 | g0053 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18969 | hp2 | a0009 | c0022 | t0002 | g0188 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18973 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18979 | hp2 | a0002 | c0005 | t0001 | g0046 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18984 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18989 | hp2 | a0001 | c0001 | t0017 | g0311 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18990 | hp1 | a0001 | c0001 | t0009 | g0019 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18995 | hp1 | a0001 | c0001 | t0009 | g0254 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19003 | hp1 | a0001 | c0001 | t0007 | g0127 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19012 | hp2 | a0001 | c0001 | t0007 | g0158 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19030 | hp1 | a0002 | c0006 | t0004 | g0006 | AFR | LWK | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19030 | hp2 | a0011 | c0013 | t0001 | g0103 | AFR | LWK | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19064 | hp1 | a0002 | c0005 | t0001 | g0056 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19064 | hp2 | a0001 | c0001 | t0016 | g0012 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19066 | hp2 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19068 | hp1 | a0002 | c0005 | t0001 | g0054 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19070 | hp2 | a0001 | c0011 | t0001 | g0016 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19076 | hp2 | a0001 | c0001 | t0009 | g0235 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19078 | hp2 | a0001 | c0011 | t0001 | g0144 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19079 | hp1 | a0002 | c0005 | t0001 | g0038 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19240 | hp1 | a0002 | c0006 | t0004 | g0032 | AFR | YRI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA19240 | hp2 | a0002 | c0002 | t0008 | g0005 | AFR | YRI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | ASW | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0217 | EUR | TSI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20752 | hp2 | a0002 | c0009 | t0003 | g0078 | EUR | TSI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20805 | hp1 | a0005 | c0021 | t0002 | g0200 | EUR | TSI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20805 | hp2 | a0001 | c0004 | t0014 | g0194 | EUR | TSI | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20905 | hp1 | a0001 | c0004 | t0005 | g0243 | SAS | GIH | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0068 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02486 | hp1 | a0002 | c0002 | t0006 | g0111 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0082 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02559 | hp1 | a0002 | c0003 | t0006 | g0117 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03471 | hp1 | a0002 | c0002 | t0006 | g0107 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | MSL | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG06807 | hp1 | a0002 | c0002 | t0011 | g0004 | AFR | USA | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
HG06807 | hp2 | a0012 | c0018 | t0008 | g0102 | AFR | USA | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20300 | hp1 | a0014 | c0016 | t0008 | g0101 | AFR | USA | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA20300 | hp2 | a0002 | c0007 | t0001 | g0088 | AFR | USA | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA21309 | hp1 | a0002 | c0005 | t0001 | g0037 | AFR | LWK | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
NA21309 | hp2 | a0001 | c0004 | t0005 | g0308 | AFR | LWK | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0265 | REF | REF | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0219 | REF | REF | PLEKHM2_chr1_15679320_15739769 | PLEKHM2 | chr1 | 15679320 | 15739769 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15716271
|
T | C | 7 | a0002a0003a0010others(4): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
missense_variant | MODERATE | c.95T>C | p.Ile32Thr | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 2/20 | 334/4134 | 95/3060 | 32/1019 | chr1 | 15716271 | ||
chr1:15725424
|
G | A | 1 | a0014 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.820G>A | p.Glu274Lys | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/20 | 1059/4134 | 820/3060 | 274/1019 | chr1 | 15725424 | ||
chr1:15725439
|
A | G | 1 | a0004 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.835A>G | p.Thr279Ala | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/20 | 1074/4134 | 835/3060 | 279/1019 | chr1 | 15725439 | ||
chr1:15725495
|
G | C | 1 | a0005 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.891G>C | p.Glu297Asp | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/20 | 1130/4134 | 891/3060 | 297/1019 | chr1 | 15725495 | ||
chr1:15727132
|
C | T | 1 | a0010 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1060C>T | p.Arg354Cys | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 9/20 | 1299/4134 | 1060/3060 | 354/1019 | chr1 | 15727132 | ||
chr1:15727156
|
C | G | 1 | a0003 | 2 | HG02257.hp1 HG02886.hp2 |
missense_variant | MODERATE | c.1084C>G | p.Arg362Gly | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 9/20 | 1323/4134 | 1084/3060 | 362/1019 | chr1 | 15727156 | ||
chr1:15727327
|
G | A | 1 | a0009 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1255G>A | p.Gly419Arg | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 9/20 | 1494/4134 | 1255/3060 | 419/1019 | chr1 | 15727327 | ||
chr1:15727358
|
G | A | 1 | a0006 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1286G>A | p.Arg429His | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 9/20 | 1525/4134 | 1286/3060 | 429/1019 | chr1 | 15727358 | ||
chr1:15727541
|
C | A | 1 | a0013 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1469C>A | p.Pro490Gln | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 9/20 | 1708/4134 | 1469/3060 | 490/1019 | chr1 | 15727541 | ||
chr1:15730545
|
C | A | 1 | a0011 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2222C>A | p.Thr741Asn | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 15/20 | 2461/4134 | 2222/3060 | 741/1019 | chr1 | 15730545 | ||
chr1:15731989
|
G | A | 1 | a0008 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.2566G>A | p.Glu856Lys | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 17/20 | 2805/4134 | 2566/3060 | 856/1019 | chr1 | 15731989 | ||
chr1:15732471
|
C | T | 1 | a0007 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2747C>T | p.Ala916Val | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 18/20 | 2986/4134 | 2747/3060 | 916/1019 | chr1 | 15732471 | ||
chr1:15733835
|
C | A | 2 | a0012a0014 | 2 | HG06807.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.2961C>A | p.Asn987Lys | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 3200/4134 | 2961/3060 | 987/1019 | chr1 | 15733835 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15717906
|
G | A | 8 | a0002c0002a0002c0005a0002c0009others(5): Show | 82 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(79): Show |
synonymous_variant | LOW | c.291G>A | p.Leu97Leu | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 4/20 | 530/4134 | 291/3060 | 97/1019 | chr1 | 15717906 | ||
chr1:15718613
|
C | T | 1 | a0001c0028 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.453C>T | p.Phe151Phe | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/20 | 692/4134 | 453/3060 | 151/1019 | chr1 | 15718613 | ||
chr1:15719829
|
C | T | 1 | a0002c0010 | 3 | HG01109.hp1 HG01255.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.561C>T | p.His187His | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/20 | 800/4134 | 561/3060 | 187/1019 | chr1 | 15719829 | ||
chr1:15725435
|
A | G | 1 | a0001c0008 | 4 | HG03942.hp2 HG04115.hp2 HG04184.hp1 others(1): Show |
synonymous_variant | LOW | c.831A>G | p.Ala277Ala | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/20 | 1070/4134 | 831/3060 | 277/1019 | chr1 | 15725435 | ||
chr1:15727314
|
C | T | 5 | a0002c0006a0002c0014a0003c0015others(2): Show | 16 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
synonymous_variant | LOW | c.1242C>T | p.Ile414Ile | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 9/20 | 1481/4134 | 1242/3060 | 414/1019 | chr1 | 15727314 | ||
chr1:15729869
|
G | A | 14 | a0001c0004a0002c0002a0002c0003others(11): Show | 115 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(112): Show |
synonymous_variant | LOW | c.2148G>A | p.Thr716Thr | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/20 | 2387/4134 | 2148/3060 | 716/1019 | chr1 | 15729869 | ||
chr1:15730534
|
A | G | 1 | a0002c0009 | 3 | HG03490.hp1 HG03492.hp2 NA20752.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2211A>G | p.Ala737Ala | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 15/20 | 2450/4134 | 2211/3060 | 737/1019 | chr1 | 15730534 | ||
chr1:15732490
|
C | T | 1 | a0001c0011 | 2 | NA19070.hp2 NA19078.hp2 |
synonymous_variant | LOW | c.2766C>T | p.Ser922Ser | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 18/20 | 3005/4134 | 2766/3060 | 922/1019 | chr1 | 15732490 | ||
chr1:15733814
|
G | A | 1 | a0001c0024 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2940G>A | p.Thr980Thr | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 3179/4134 | 2940/3060 | 980/1019 | chr1 | 15733814 | ||
chr1:15733823
|
G | A | 1 | a0002c0012 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2949G>A | p.Gln983Gln | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 3188/4134 | 2949/3060 | 983/1019 | chr1 | 15733823 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15684398
|
C | T | 9 | a0002c0002t0008a0002c0002t0011a0002c0002t0012others(6): Show | 16 | HG00642.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-161C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/20 | 161 | chr1 | 15684398 | |||||
chr1:15684510
|
G | GGGC | 35 | a0001c0001t0001a0001c0001t0015a0001c0001t0016others(32): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-35dupCGG | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/20 | 34 | INFO_REALIGN_3_PRIME | chr1 | 15684510 | ||||
chr1:15684516
|
CGGCGGCG others(8): Show |
C | 1 | a0002c0003t0019 | 1 | HG02895.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37_-23delCGGTGGCG others(7): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/20 | 23 | INFO_REALIGN_3_PRIME | chr1 | 15684516 | ||||
chr1:15684519
|
C | CGGCGGCG others(8): Show |
1 | a0002c0002t0013 | 2 | HG02976.hp2 HG03453.hp1 |
5_prime_UTR_variant | MODIFIER | c.-35_-34insCGGTGGCG others(7): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/20 | 34 | INFO_REALIGN_3_PRIME | chr1 | 15684519 | ||||
chr1:15684525
|
T | C | 1 | a0002c0002t0011 | 3 | HG03540.hp2 HG03579.hp1 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-34T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/20 | 34 | chr1 | 15684525 | |||||
chr1:15734003
|
G | A | 9 | a0002c0002t0008a0002c0002t0010a0002c0002t0011others(6): Show | 16 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 69 | chr1 | 15734003 | |||||
chr1:15734077
|
A | G | 1 | a0001c0001t0016 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 143 | chr1 | 15734077 | |||||
chr1:15734116
|
G | A | 1 | a0001c0001t0017 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*182G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 182 | chr1 | 15734116 | |||||
chr1:15734148
|
G | A | 1 | a0001c0004t0014 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 214 | chr1 | 15734148 | |||||
chr1:15734183
|
T | C | 11 | a0001c0001t0005a0001c0004t0003a0001c0004t0005others(8): Show | 66 | HG00280.hp1 HG00639.hp2 HG01106.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*249T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 249 | chr1 | 15734183 | |||||
chr1:15734397
|
C | T | 9 | a0001c0001t0017a0002c0002t0004a0002c0002t0012others(6): Show | 25 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*463C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 463 | chr1 | 15734397 | |||||
chr1:15734416
|
C | T | 1 | a0001c0001t0015 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 482 | chr1 | 15734416 | |||||
chr1:15734440
|
A | G | 1 | a0002c0003t0020 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 506 | chr1 | 15734440 | |||||
chr1:15734462
|
G | A | 1 | a0001c0001t0009 | 4 | NA18943.hp1 NA18990.hp1 NA18995.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 528 | chr1 | 15734462 | |||||
chr1:15734540
|
G | C | 31 | a0001c0001t0005a0001c0001t0017a0001c0004t0003others(28): Show | 116 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*606G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 606 | chr1 | 15734540 | |||||
chr1:15734628
|
A | G | 1 | a0001c0001t0007 | 7 | HG02074.hp1 NA18952.hp1 NA18971.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*694A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 20/20 | 694 | chr1 | 15734628 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15684697
|
G | GGCGACCC others(17): Show |
112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.60+80_60+81insCGAC others(20): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15684697 | |||||
chr1:15684721
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.60+103C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15684721 | ||||||
chr1:15684779
|
G | T | 1 | a0003c0019t0004g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.60+161G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15684779 | ||||||
chr1:15684877
|
C | T | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.60+259C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15684877 | ||||||
chr1:15685034
|
G | A | 13 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(10): Show | 14 | HG00642.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+416G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685034 | ||||||
chr1:15685037
|
A | G | 1 | a0003c0019t0004g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.60+419A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685037 | ||||||
chr1:15685119
|
C | T | 1 | a0001c0001t0002g0310 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.60+501C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685119 | ||||||
chr1:15685225
|
C | A | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.60+607C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685225 | ||||||
chr1:15685397
|
A | AAAT | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+791_60+793dupTA others(1): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15685397 | |||||
chr1:15685541
|
G | GA | 65 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(62): Show | 71 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.60+942dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15685541 | |||||
chr1:15685541
|
G | GAA | 8 | a0002c0005t0001g0037a0002c0005t0001g0038a0002c0006t0004g0006others(5): Show | 9 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.60+941_60+942dupAA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15685541 | |||||
chr1:15685541
|
GA | G | 13 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0002g0300others(10): Show | 13 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.60+942delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15685541 | |||||
chr1:15685557
|
A | AG | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+939_60+940insG | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685557 | ||||||
chr1:15685586
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0134a0001c0001t0002g0135others(2): Show | 5 | HG00735.hp2 HG01123.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+968G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685586 | ||||||
chr1:15685678
|
TTGTC | T | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0020g0024 | 3 | HG00642.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.60+1064_60+1067del others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15685678 | |||||
chr1:15685938
|
A | C | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.60+1320A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685938 | ||||||
chr1:15685965
|
G | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0004c0027t0001g0297 | 3 | HG00140.hp1 HG00741.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.60+1347G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685965 | ||||||
chr1:15685978
|
C | T | 5 | a0001c0001t0002g0021a0001c0001t0002g0293a0001c0001t0002g0295others(2): Show | 6 | HG02258.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+1360C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685978 | ||||||
chr1:15685998
|
C | A | 23 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(20): Show | 25 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.60+1380C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15685998 | ||||||
chr1:15686054
|
G | A | 2 | a0002c0002t0006g0113a0002c0002t0006g0114 | 2 | HG01243.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.60+1436G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686054 | ||||||
chr1:15686162
|
T | C | 23 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(20): Show | 25 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.60+1544T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686162 | ||||||
chr1:15686172
|
G | A | 3 | a0002c0002t0003g0039a0002c0002t0003g0040a0002c0002t0003g0041 | 3 | HG03139.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.60+1554G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686172 | ||||||
chr1:15686272
|
C | T | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.60+1654C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686272 | ||||||
chr1:15686322
|
T | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.60+1704T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686322 | ||||||
chr1:15686468
|
T | G | 2 | a0002c0002t0010g0100a0002c0014t0004g0036 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.60+1850T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686468 | ||||||
chr1:15686471
|
G | T | 2 | a0001c0001t0002g0291a0001c0001t0002g0292 | 2 | HG01943.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.60+1853G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686471 | ||||||
chr1:15686501
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.60+1883G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686501 | ||||||
chr1:15686601
|
C | T | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.60+1983C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686601 | ||||||
chr1:15686647
|
A | ATTT | 4 | a0002c0002t0004g0043a0002c0002t0010g0100a0002c0005t0001g0042others(1): Show | 4 | HG01069.hp2 HG01109.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+2029_60+2030ins others(3): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686647 | ||||||
chr1:15686647
|
A | ATTTT | 57 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(54): Show | 63 | HG00639.hp2 HG01071.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.60+2029_60+2030ins others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686647 | ||||||
chr1:15686647
|
A | ATTTTT | 6 | a0002c0002t0003g0081a0002c0002t0003g0082a0002c0002t0003g0083others(3): Show | 6 | HG02056.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+2029_60+2030ins others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686647 | ||||||
chr1:15686648
|
A | ATT | 8 | a0002c0006t0004g0006a0002c0006t0004g0033a0002c0006t0004g0034others(5): Show | 9 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.60+2047_60+2048dup others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686648
|
A | ATTTTTTT others(12): Show |
1 | a0002c0002t0008g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.60+2048_60+2049ins others(19): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686648
|
A | ATTTTTTT others(13): Show |
3 | a0002c0002t0008g0030a0002c0002t0011g0004a0002c0002t0013g0029 | 4 | HG02976.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+2048_60+2049ins others(20): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686648
|
A | ATTTTTTT others(14): Show |
3 | a0002c0002t0008g0005a0002c0002t0011g0005a0002c0002t0013g0031 | 3 | HG03453.hp1 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.60+2048_60+2049ins others(21): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686648
|
A | ATTTTTTT others(20): Show |
1 | a0003c0015t0012g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.60+2048_60+2049ins others(27): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686648
|
A | ATTTTTTT others(26): Show |
1 | a0002c0002t0012g0026 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.60+2048_60+2049ins others(33): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686648
|
A | ATTTTTTT others(27): Show |
1 | a0002c0002t0012g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.60+2048_60+2049ins others(34): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686648
|
A | T | 69 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 75 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.60+2030A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686648 | ||||||
chr1:15686648
|
AT | A | 8 | a0001c0001t0002g0021a0001c0001t0002g0124a0001c0001t0002g0293others(5): Show | 9 | HG02258.hp1 HG02965.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.60+2048delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15686648 | |||||
chr1:15686687
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.60+2069C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686687 | ||||||
chr1:15686751
|
C | T | 10 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(7): Show | 10 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+2133C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686751 | ||||||
chr1:15686808
|
C | T | 1 | a0010c0020t0001g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.60+2190C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686808 | ||||||
chr1:15686875
|
C | T | 2 | a0001c0001t0002g0288a0001c0001t0002g0289 | 2 | HG02080.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.60+2257C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686875 | ||||||
chr1:15686953
|
A | T | 23 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(20): Show | 25 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.60+2335A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15686953 | ||||||
chr1:15687083
|
C | A | 3 | a0002c0002t0006g0113a0002c0002t0006g0114a0002c0006t0004g0085 | 3 | HG01243.hp2 HG02809.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.60+2465C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687083 | ||||||
chr1:15687083
|
C | T | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0020g0024 | 3 | HG00642.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.60+2465C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687083 | ||||||
chr1:15687114
|
G | T | 8 | a0001c0001t0002g0133a0001c0001t0002g0281a0001c0001t0002g0282others(5): Show | 8 | HG01243.hp1 HG01358.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+2496G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687114 | ||||||
chr1:15687119
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.60+2501C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687119 | ||||||
chr1:15687120
|
GC | G | 69 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 75 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.60+2505delC | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15687120 | |||||
chr1:15687240
|
C | T | 1 | a0001c0004t0005g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.60+2622C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687240 | ||||||
chr1:15687316
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.60+2698G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687316 | ||||||
chr1:15687322
|
C | T | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.60+2704C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687322 | ||||||
chr1:15687357
|
G | A | 2 | a0002c0002t0003g0044a0002c0002t0003g0045 | 2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.60+2739G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687357 | ||||||
chr1:15687417
|
G | A | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+2799G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687417 | ||||||
chr1:15687426
|
G | C | 3 | a0002c0002t0012g0026a0002c0002t0012g0027a0003c0015t0012g0025 | 3 | HG01891.hp1 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60+2808G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687426 | ||||||
chr1:15687633
|
C | T | 36 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(33): Show | 40 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.60+3015C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687633 | ||||||
chr1:15687778
|
A | T | 4 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277others(1): Show | 4 | HG00438.hp2 NA18994.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+3160A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687778 | ||||||
chr1:15687863
|
A | G | 1 | a0002c0003t0020g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.60+3245A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687863 | ||||||
chr1:15687963
|
A | T | 1 | a0002c0003t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.60+3345A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15687963 | ||||||
chr1:15688226
|
T | A | 1 | a0010c0020t0001g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.60+3608T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15688226 | ||||||
chr1:15688263
|
C | G | 1 | a0001c0001t0001g0274 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.60+3645C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15688263 | ||||||
chr1:15688521
|
G | A | 10 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(7): Show | 10 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+3903G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15688521 | ||||||
chr1:15688523
|
G | A | 1 | a0003c0015t0012g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.60+3905G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15688523 | ||||||
chr1:15688607
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.60+3989G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15688607 | ||||||
chr1:15688649
|
C | CA | 7 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0002g0124others(4): Show | 7 | HG01192.hp1 HG02080.hp1 NA19076.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+4049dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15688649 | |||||
chr1:15688649
|
CA | C | 106 | a0001c0001t0001g0272a0001c0001t0001g0273a0002c0002t0003g0001others(103): Show | 115 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(112): Show |
intron_variant | MODIFIER | c.60+4049delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15688649 | |||||
chr1:15688824
|
T | C | 46 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(43): Show | 51 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.60+4206T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15688824 | ||||||
chr1:15688959
|
A | G | 3 | a0002c0007t0001g0094a0002c0007t0001g0095a0002c0007t0001g0112 | 3 | HG00323.hp1 HG01069.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.60+4341A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15688959 | ||||||
chr1:15689015
|
G | A | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.60+4397G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689015 | ||||||
chr1:15689032
|
T | C | 36 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(33): Show | 40 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.60+4414T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689032 | ||||||
chr1:15689087
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0274a0001c0001t0015g0003others(1): Show | 5 | HG01168.hp1 HG01192.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+4469A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689087 | ||||||
chr1:15689102
|
G | A | 2 | a0002c0002t0010g0100a0002c0014t0004g0036 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.60+4484G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689102 | ||||||
chr1:15689108
|
T | C | 46 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(43): Show | 51 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.60+4490T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689108 | ||||||
chr1:15689143
|
G | A | 11 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(8): Show | 13 | HG01167.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.60+4525G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689143 | ||||||
chr1:15689245
|
C | CA | 60 | a0001c0001t0002g0291a0001c0001t0007g0127a0002c0002t0003g0007others(57): Show | 65 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.60+4643dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15689245 | |||||
chr1:15689245
|
C | CAA | 40 | a0002c0002t0003g0047a0002c0002t0003g0048a0002c0002t0003g0050others(37): Show | 42 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.60+4642_60+4643dup others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15689245 | |||||
chr1:15689245
|
C | CAAA | 9 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(6): Show | 11 | HG01167.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+4641_60+4643dup others(3): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15689245 | |||||
chr1:15689262
|
G | A | 5 | a0002c0003t0003g0116a0002c0003t0003g0118a0002c0003t0003g0119others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+4644G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689262 | ||||||
chr1:15689289
|
G | A | 43 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(40): Show | 46 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.60+4671G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689289 | ||||||
chr1:15689372
|
G | A | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+4754G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689372 | ||||||
chr1:15689491
|
C | A | 46 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(43): Show | 51 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.60+4873C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689491 | ||||||
chr1:15689673
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.60+5055A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689673 | ||||||
chr1:15689675
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.60+5057A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689675 | ||||||
chr1:15689701
|
G | A | 1 | a0002c0002t0003g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.60+5083G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689701 | ||||||
chr1:15689767
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.60+5149T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689767 | ||||||
chr1:15689783
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.60+5165T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689783 | ||||||
chr1:15689793
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.60+5175G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689793 | ||||||
chr1:15689794
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.60+5176T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689794 | ||||||
chr1:15689849
|
C | G | 1 | a0001c0001t0002g0270 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.60+5231C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689849 | ||||||
chr1:15689881
|
C | T | 69 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 75 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.60+5263C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689881 | ||||||
chr1:15689936
|
A | G | 1 | a0002c0007t0001g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.60+5318A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15689936 | ||||||
chr1:15690056
|
G | A | 23 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(20): Show | 25 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.60+5438G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690056 | ||||||
chr1:15690059
|
G | GT | 14 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(11): Show | 14 | HG00438.hp1 HG00438.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+5455dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15690059 | |||||
chr1:15690069
|
T | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0001g0132others(99): Show | 110 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.60+5451T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690069 | ||||||
chr1:15690069
|
T | TG | 23 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(20): Show | 25 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.60+5451_60+5452ins others(1): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690069 | ||||||
chr1:15690070
|
T | G | 6 | a0001c0001t0002g0133a0001c0001t0002g0156a0001c0001t0002g0281others(3): Show | 6 | HG01243.hp1 HG01358.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+5452T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690070 | ||||||
chr1:15690071
|
T | G | 1 | a0001c0001t0002g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.60+5453T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690071 | ||||||
chr1:15690073
|
T | G | 1 | a0001c0001t0007g0158 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.60+5455T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690073 | ||||||
chr1:15690074
|
G | T | 60 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(57): Show | 62 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.60+5456G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690074 | ||||||
chr1:15690075
|
T | G | 7 | a0001c0001t0002g0157a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG00735.hp1 HG00738.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+5457T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690075 | ||||||
chr1:15690156
|
T | G | 10 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(7): Show | 10 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+5538T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690156 | ||||||
chr1:15690207
|
G | A | 69 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 75 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.60+5589G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690207 | ||||||
chr1:15690282
|
T | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(63): Show | 72 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.60+5664T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690282 | ||||||
chr1:15690577
|
G | A | 1 | a0002c0003t0003g0120 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.60+5959G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690577 | ||||||
chr1:15690580
|
G | A | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.60+5962G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690580 | ||||||
chr1:15690994
|
G | C | 1 | a0002c0002t0008g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.60+6376G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15690994 | ||||||
chr1:15691181
|
C | T | 23 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(20): Show | 25 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.60+6563C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15691181 | ||||||
chr1:15691182
|
G | A | 2 | a0001c0001t0002g0159a0001c0001t0002g0270 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.60+6564G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15691182 | ||||||
chr1:15691215
|
A | G | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.60+6597A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15691215 | ||||||
chr1:15691311
|
A | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0131a0001c0001t0001g0145others(3): Show | 7 | HG02129.hp2 HG02165.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+6693A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15691311 | ||||||
chr1:15691581
|
C | G | 33 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(30): Show | 35 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.60+6963C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15691581 | ||||||
chr1:15691781
|
T | G | 4 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(1): Show | 6 | HG01167.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+7163T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15691781 | ||||||
chr1:15691825
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.60+7207G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15691825 | ||||||
chr1:15692049
|
G | A | 60 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(57): Show | 66 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.60+7431G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15692049 | ||||||
chr1:15692113
|
G | A | 69 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 75 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.60+7495G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15692113 | ||||||
chr1:15692471
|
G | C | 1 | a0001c0001t0002g0240 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.60+7853G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15692471 | ||||||
chr1:15692551
|
T | C | 1 | a0010c0020t0001g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.60+7933T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15692551 | ||||||
chr1:15692576
|
T | C | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+7958T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15692576 | ||||||
chr1:15692611
|
G | T | 1 | a0001c0004t0005g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.60+7993G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15692611 | ||||||
chr1:15692719
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.60+8101A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15692719 | ||||||
chr1:15693005
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(63): Show | 72 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.60+8387C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693005 | ||||||
chr1:15693018
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.60+8400C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693018 | ||||||
chr1:15693076
|
C | T | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+8458C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693076 | ||||||
chr1:15693226
|
G | A | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.60+8608G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693226 | ||||||
chr1:15693466
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.60+8848C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693466 | ||||||
chr1:15693469
|
T | C | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0020g0024 | 3 | HG00642.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.60+8851T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693469 | ||||||
chr1:15693475
|
C | A | 1 | a0001c0001t0002g0266 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.60+8857C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693475 | ||||||
chr1:15693741
|
A | G | 1 | a0001c0004t0005g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.60+9123A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15693741 | ||||||
chr1:15694007
|
G | A | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.60+9389G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694007 | ||||||
chr1:15694125
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0002g0228a0001c0001t0002g0290 | 3 | HG00140.hp2 HG00741.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.60+9507G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694125 | ||||||
chr1:15694181
|
G | A | 3 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0292 | 3 | HG01943.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.60+9563G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694181 | ||||||
chr1:15694287
|
C | T | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.60+9669C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694287 | ||||||
chr1:15694305
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0145a0001c0001t0001g0229 | 3 | NA18951.hp1 NA18960.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.60+9687C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694305 | ||||||
chr1:15694327
|
C | T | 1 | a0002c0002t0003g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.60+9709C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694327 | ||||||
chr1:15694348
|
C | A | 56 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0138others(53): Show | 58 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.60+9730C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694348 | ||||||
chr1:15694348
|
C | CA | 12 | a0002c0002t0003g0061a0002c0002t0003g0105a0002c0002t0008g0005others(9): Show | 13 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.60+9740dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15694348 | |||||
chr1:15694380
|
C | A | 4 | a0002c0002t0006g0106a0002c0002t0006g0107a0002c0002t0006g0108others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+9762C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694380 | ||||||
chr1:15694421
|
T | A | 1 | a0007c0025t0002g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.60+9803T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694421 | ||||||
chr1:15694476
|
C | G | 1 | a0012c0018t0008g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.60+9858C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694476 | ||||||
chr1:15694756
|
G | GT | 73 | a0001c0001t0001g0132a0001c0001t0001g0155a0001c0001t0001g0226others(70): Show | 79 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.60+10150dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15694756 | |||||
chr1:15694756
|
GT | G | 11 | a0001c0001t0002g0124a0002c0002t0008g0005a0002c0002t0008g0028others(8): Show | 12 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.60+10150delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15694756 | |||||
chr1:15694797
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.60+10179G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694797 | ||||||
chr1:15694806
|
G | C | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.60+10188G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694806 | ||||||
chr1:15694824
|
T | C | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.60+10206T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694824 | ||||||
chr1:15694982
|
T | C | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0020g0024 | 3 | HG00642.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.60+10364T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15694982 | ||||||
chr1:15695061
|
T | C | 1 | a0003c0019t0004g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.60+10443T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695061 | ||||||
chr1:15695172
|
A | T | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+10554A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695172 | ||||||
chr1:15695349
|
G | C | 1 | a0002c0002t0008g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.60+10731G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695349 | ||||||
chr1:15695388
|
G | A | 1 | a0002c0002t0006g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.60+10770G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695388 | ||||||
chr1:15695494
|
A | G | 1 | a0001c0004t0005g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.60+10876A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695494 | ||||||
chr1:15695657
|
G | A | 10 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(7): Show | 10 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+11039G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695657 | ||||||
chr1:15695774
|
G | T | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0020g0024 | 3 | HG00642.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.60+11156G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695774 | ||||||
chr1:15695793
|
C | T | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.60+11175C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695793 | ||||||
chr1:15695882
|
GC | G | 9 | a0001c0001t0002g0021a0001c0001t0002g0130a0001c0001t0002g0223others(6): Show | 10 | HG02145.hp1 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+11266delC | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15695882 | |||||
chr1:15695911
|
C | T | 1 | a0002c0003t0004g0093 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.60+11293C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695911 | ||||||
chr1:15695980
|
AT | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(188): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.60+11377delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15695980 | |||||
chr1:15695980
|
ATT | A | 103 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(100): Show | 111 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.60+11376_60+11377d others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15695980 | |||||
chr1:15695980
|
ATTT | A | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+11375_60+11377d others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15695980 | |||||
chr1:15695984
|
T | A | 1 | a0002c0014t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.60+11366T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15695984 | ||||||
chr1:15696265
|
T | C | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0020g0024 | 3 | HG00642.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.60+11647T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15696265 | ||||||
chr1:15696438
|
T | C | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.60+11820T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15696438 | ||||||
chr1:15696476
|
G | A | 1 | a0001c0001t0002g0268 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.60+11858G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15696476 | ||||||
chr1:15696508
|
G | A | 10 | a0001c0001t0002g0021a0001c0001t0002g0130a0001c0001t0002g0223others(7): Show | 11 | HG02145.hp1 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.60+11890G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15696508 | ||||||
chr1:15696600
|
C | T | 8 | a0001c0001t0001g0016a0001c0001t0001g0215a0001c0001t0001g0216others(5): Show | 8 | HG00438.hp1 HG02056.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+11982C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15696600 | ||||||
chr1:15696630
|
C | T | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+12012C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15696630 | ||||||
chr1:15697004
|
T | A | 1 | a0001c0004t0005g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.60+12386T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697004 | ||||||
chr1:15697034
|
G | C | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092 | 3 | HG00642.hp2 HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.60+12416G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697034 | ||||||
chr1:15697035
|
G | A | 22 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(19): Show | 24 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.60+12417G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697035 | ||||||
chr1:15697193
|
G | A | 1 | a0001c0028t0002g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.60+12575G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697193 | ||||||
chr1:15697242
|
C | T | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092 | 3 | HG00642.hp2 HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.60+12624C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697242 | ||||||
chr1:15697406
|
A | G | 3 | a0002c0002t0012g0026a0002c0002t0012g0027a0003c0015t0012g0025 | 3 | HG01891.hp1 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60+12788A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697406 | ||||||
chr1:15697470
|
G | A | 3 | a0002c0007t0001g0094a0002c0007t0001g0095a0002c0007t0001g0112 | 3 | HG00323.hp1 HG01069.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.60+12852G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697470 | ||||||
chr1:15697694
|
C | T | 22 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(19): Show | 24 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.60+13076C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697694 | ||||||
chr1:15697741
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.60+13123C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697741 | ||||||
chr1:15697784
|
C | T | 2 | a0002c0002t0004g0010a0002c0002t0004g0043 | 3 | HG01069.hp2 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.60+13166C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697784 | ||||||
chr1:15697785
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.60+13167C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15697785 | ||||||
chr1:15698042
|
A | G | 3 | a0002c0002t0012g0026a0002c0002t0012g0027a0003c0015t0012g0025 | 3 | HG01891.hp1 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60+13424A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698042 | ||||||
chr1:15698043
|
G | T | 1 | a0002c0002t0003g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.60+13425G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698043 | ||||||
chr1:15698055
|
A | AT | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+13438dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698055 | |||||
chr1:15698201
|
ATTTTTAT | A | 3 | a0001c0001t0002g0157a0012c0018t0008g0102a0014c0016t0008g0101 | 3 | HG02109.hp1 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.60+13602_60+13608d others(9): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698201 | |||||
chr1:15698474
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.60+13856G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698474 | ||||||
chr1:15698529
|
TTTTC | T | 3 | a0001c0001t0002g0304a0002c0002t0012g0026a0003c0015t0012g0025 | 3 | HG00099.hp1 HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.60+13931_60+13934d others(6): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698529 | |||||
chr1:15698541
|
C | CT | 3 | a0002c0003t0003g0118a0012c0018t0008g0102a0014c0016t0008g0101 | 3 | HG03139.hp1 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.60+13926dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698541 | |||||
chr1:15698541
|
C | CTTT | 5 | a0002c0002t0008g0005a0002c0002t0011g0004a0002c0002t0011g0005others(2): Show | 6 | HG02976.hp2 HG03453.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+13924_60+13926d others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698541 | |||||
chr1:15698541
|
C | T | 1 | a0002c0002t0008g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.60+13923C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698541 | ||||||
chr1:15698541
|
CTTTCTTT others(3): Show |
C | 2 | a0002c0006t0004g0085a0002c0006t0004g0091 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.60+13927_60+13936d others(12): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698541 | |||||
chr1:15698541
|
CTTTCTTT others(4): Show |
C | 20 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(17): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.60+13927_60+13937d others(13): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698541 | |||||
chr1:15698545
|
C | T | 16 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(13): Show | 17 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.60+13927C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698545 | ||||||
chr1:15698549
|
C | CT | 6 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0269others(3): Show | 6 | HG01168.hp2 HG01943.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+13949dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698549 | |||||
chr1:15698549
|
C | T | 19 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(16): Show | 20 | HG01891.hp1 HG02257.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.60+13931C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698549 | ||||||
chr1:15698549
|
CT | C | 9 | a0001c0001t0001g0145a0001c0001t0001g0165a0001c0001t0001g0263others(6): Show | 9 | HG00099.hp2 HG01070.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.60+13949delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698549 | |||||
chr1:15698549
|
CTT | C | 65 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(62): Show | 71 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.60+13948_60+13949d others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15698549 | |||||
chr1:15698604
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.60+13986A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698604 | ||||||
chr1:15698672
|
C | T | 2 | a0001c0001t0002g0262a0001c0001t0002g0267 | 2 | NA18975.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.60+14054C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698672 | ||||||
chr1:15698695
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.60+14077G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698695 | ||||||
chr1:15698706
|
C | G | 1 | a0002c0002t0006g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.60+14088C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698706 | ||||||
chr1:15698835
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.60+14217C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698835 | ||||||
chr1:15698847
|
C | T | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.60+14229C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698847 | ||||||
chr1:15698859
|
A | T | 3 | a0002c0002t0006g0111a0002c0002t0006g0113a0002c0002t0006g0114 | 3 | HG01243.hp2 HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.60+14241A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698859 | ||||||
chr1:15698892
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.60+14274G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15698892 | ||||||
chr1:15699218
|
A | T | 2 | a0002c0007t0001g0095a0002c0007t0001g0112 | 2 | HG00323.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.60+14600A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15699218 | ||||||
chr1:15699218
|
ATGTGCAG others(14): Show |
A | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.60+14625_60+14645d others(23): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15699218 | |||||
chr1:15699349
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.60+14731C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15699349 | ||||||
chr1:15699710
|
G | A | 2 | a0002c0009t0003g0072a0002c0009t0003g0073 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.60+15092G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15699710 | ||||||
chr1:15699783
|
G | T | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.60+15165G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15699783 | ||||||
chr1:15699990
|
CA | C | 44 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(41): Show | 47 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.60+15384delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15699990 | |||||
chr1:15700003
|
C | A | 1 | a0001c0004t0005g0241 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.60+15385C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700003 | ||||||
chr1:15700122
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.60+15504C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700122 | ||||||
chr1:15700364
|
T | C | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.60+15746T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700364 | ||||||
chr1:15700479
|
G | A | 5 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | NA18939.hp1 NA18963.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.61-15758G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700479 | ||||||
chr1:15700486
|
C | G | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61-15751C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700486 | ||||||
chr1:15700611
|
C | T | 69 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 75 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.61-15626C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700611 | ||||||
chr1:15700620
|
A | C | 1 | a0001c0001t0002g0212 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.61-15617A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700620 | ||||||
chr1:15700671
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.61-15566T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700671 | ||||||
chr1:15700734
|
C | T | 1 | a0001c0004t0003g0015 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.61-15503C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700734 | ||||||
chr1:15700803
|
C | T | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-15434C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700803 | ||||||
chr1:15700842
|
G | A | 1 | a0002c0003t0020g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.61-15395G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700842 | ||||||
chr1:15700898
|
G | A | 22 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(19): Show | 24 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.61-15339G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15700898 | ||||||
chr1:15701113
|
C | CA | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(159): Show | 174 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.61-15108dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15701113 | |||||
chr1:15701113
|
C | CAAAA | 20 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(17): Show | 21 | HG01891.hp1 HG02257.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.61-15111_61-15108d others(6): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15701113 | |||||
chr1:15701113
|
C | CAAAAA | 20 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(17): Show | 22 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.61-15112_61-15108d others(7): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15701113 | |||||
chr1:15701113
|
CA | C | 11 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0267others(8): Show | 12 | HG00544.hp1 HG02074.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-15108delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15701113 | |||||
chr1:15701170
|
T | G | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.61-15067T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701170 | ||||||
chr1:15701189
|
G | A | 1 | a0002c0002t0003g0051 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61-15048G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701189 | ||||||
chr1:15701250
|
G | A | 1 | a0002c0002t0003g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.61-14987G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701250 | ||||||
chr1:15701327
|
A | G | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.61-14910A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701327 | ||||||
chr1:15701424
|
A | C | 1 | a0001c0001t0001g0216 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.61-14813A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701424 | ||||||
chr1:15701538
|
C | T | 60 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(57): Show | 66 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-14699C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701538 | ||||||
chr1:15701652
|
G | C | 2 | a0002c0007t0001g0095a0002c0007t0001g0112 | 2 | HG00323.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.61-14585G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701652 | ||||||
chr1:15701716
|
G | A | 1 | a0002c0002t0008g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.61-14521G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701716 | ||||||
chr1:15701722
|
C | T | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61-14515C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701722 | ||||||
chr1:15701781
|
A | G | 1 | a0002c0002t0003g0057 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.61-14456A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701781 | ||||||
chr1:15701829
|
A | G | 3 | a0002c0002t0012g0026a0002c0002t0012g0027a0003c0015t0012g0025 | 3 | HG01891.hp1 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.61-14408A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701829 | ||||||
chr1:15701878
|
T | G | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.61-14359T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701878 | ||||||
chr1:15701953
|
G | T | 6 | a0001c0001t0002g0125a0001c0001t0002g0134a0001c0001t0002g0135others(3): Show | 6 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-14284G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15701953 | ||||||
chr1:15702060
|
C | T | 3 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084 | 5 | HG01167.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-14177C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702060 | ||||||
chr1:15702183
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.61-14054A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702183 | ||||||
chr1:15702217
|
G | A | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61-14020G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702217 | ||||||
chr1:15702266
|
T | C | 1 | a0001c0008t0002g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.61-13971T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702266 | ||||||
chr1:15702322
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(82): Show | 90 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.61-13915G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702322 | ||||||
chr1:15702354
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.61-13883G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702354 | ||||||
chr1:15702630
|
C | T | 1 | a0002c0002t0006g0114 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.61-13607C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702630 | ||||||
chr1:15702671
|
A | G | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.61-13566A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702671 | ||||||
chr1:15702679
|
A | G | 1 | a0003c0019t0004g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.61-13558A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702679 | ||||||
chr1:15702681
|
G | A | 1 | a0001c0004t0005g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.61-13556G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702681 | ||||||
chr1:15702717
|
C | CT | 28 | a0001c0001t0001g0195a0001c0001t0001g0214a0001c0001t0001g0238others(25): Show | 28 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.61-13500dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15702717 | |||||
chr1:15702717
|
CT | C | 92 | a0001c0001t0002g0199a0001c0001t0017g0311a0002c0002t0003g0001others(89): Show | 100 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.61-13500delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15702717 | |||||
chr1:15702717
|
CTT | C | 13 | a0002c0002t0003g0061a0002c0002t0003g0105a0002c0002t0008g0005others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-13501_61-13500d others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15702717 | |||||
chr1:15702891
|
TA | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG01081.hp2 NA18747.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-13333delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15702891 | |||||
chr1:15702907
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.61-13330T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702907 | ||||||
chr1:15702974
|
G | A | 2 | a0001c0001t0002g0251a0002c0003t0020g0024 | 2 | HG00280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.61-13263G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15702974 | ||||||
chr1:15703021
|
C | T | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-13216C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15703021 | ||||||
chr1:15703214
|
G | A | 3 | a0002c0002t0006g0111a0002c0002t0006g0113a0002c0002t0006g0114 | 3 | HG01243.hp2 HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.61-13023G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15703214 | ||||||
chr1:15703331
|
A | G | 1 | a0002c0002t0003g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.61-12906A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15703331 | ||||||
chr1:15703347
|
C | CTGT | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.61-12884_61-12882d others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15703347 | |||||
chr1:15703422
|
C | T | 3 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084 | 5 | HG01167.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-12815C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15703422 | ||||||
chr1:15703881
|
T | G | 2 | a0002c0002t0010g0100a0002c0014t0004g0036 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.61-12356T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15703881 | ||||||
chr1:15703887
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0134a0001c0001t0002g0135others(2): Show | 5 | HG00735.hp2 HG01123.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-12350G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15703887 | ||||||
chr1:15704013
|
C | G | 1 | a0001c0001t0002g0277 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.61-12224C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704013 | ||||||
chr1:15704028
|
A | T | 2 | a0002c0002t0006g0108a0002c0002t0006g0109 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.61-12209A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704028 | ||||||
chr1:15704149
|
G | A | 1 | a0002c0002t0003g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61-12088G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704149 | ||||||
chr1:15704210
|
TTACTC | T | 70 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(67): Show | 76 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.61-12023_61-12019d others(7): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15704210 | |||||
chr1:15704226
|
T | C | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.61-12011T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704226 | ||||||
chr1:15704250
|
C | T | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-11987C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704250 | ||||||
chr1:15704308
|
CCCTCCCT others(1): Show |
C | 4 | a0001c0001t0001g0131a0001c0001t0001g0145a0001c0001t0001g0229others(1): Show | 4 | NA18951.hp1 NA18960.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-11917_61-11910d others(10): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15704308 | |||||
chr1:15704431
|
C | T | 69 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(66): Show | 75 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.61-11806C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704431 | ||||||
chr1:15704726
|
T | C | 1 | a0002c0006t0004g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.61-11511T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704726 | ||||||
chr1:15704858
|
G | A | 1 | a0005c0021t0002g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-11379G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704858 | ||||||
chr1:15704872
|
C | T | 60 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(57): Show | 66 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-11365C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704872 | ||||||
chr1:15704899
|
C | T | 2 | a0002c0005t0001g0042a0002c0005t0001g0056 | 2 | NA18954.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.61-11338C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15704899 | ||||||
chr1:15705023
|
C | T | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-11214C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705023 | ||||||
chr1:15705034
|
G | A | 1 | a0002c0014t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.61-11203G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705034 | ||||||
chr1:15705075
|
A | G | 1 | a0001c0004t0005g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.61-11162A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705075 | ||||||
chr1:15705104
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.61-11133C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705104 | ||||||
chr1:15705162
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.61-11075G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705162 | ||||||
chr1:15705170
|
C | CT | 16 | a0001c0001t0001g0146a0001c0001t0001g0192a0001c0001t0001g0193others(13): Show | 16 | HG00438.hp2 HG00738.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-11040dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15705170 | |||||
chr1:15705170
|
CT | C | 89 | a0001c0001t0001g0145a0001c0001t0001g0164a0001c0001t0001g0171others(86): Show | 96 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.61-11040delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15705170 | |||||
chr1:15705170
|
CTT | C | 17 | a0001c0001t0002g0252a0002c0002t0003g0044a0002c0002t0003g0058others(14): Show | 18 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.61-11041_61-11040d others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15705170 | |||||
chr1:15705170
|
CTTT | C | 12 | a0002c0002t0006g0104a0002c0002t0008g0005a0002c0002t0008g0028others(9): Show | 13 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-11042_61-11040d others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15705170 | |||||
chr1:15705170
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61-11049_61-11040d others(12): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15705170 | |||||
chr1:15705170
|
CTTTTTTT others(5): Show |
C | 1 | a0005c0021t0002g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-11051_61-11040d others(14): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15705170 | |||||
chr1:15705396
|
T | G | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.61-10841T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705396 | ||||||
chr1:15705428
|
C | T | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61-10809C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705428 | ||||||
chr1:15705461
|
C | T | 1 | a0002c0002t0010g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.61-10776C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705461 | ||||||
chr1:15705472
|
G | A | 1 | a0002c0006t0004g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61-10765G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705472 | ||||||
chr1:15705523
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0155 | 2 | NA18966.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.61-10714G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705523 | ||||||
chr1:15705529
|
C | A | 1 | a0002c0006t0004g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.61-10708C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705529 | ||||||
chr1:15705547
|
C | T | 6 | a0001c0001t0002g0125a0001c0001t0002g0134a0001c0001t0002g0135others(3): Show | 6 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-10690C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705547 | ||||||
chr1:15705554
|
C | T | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10683C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705554 | ||||||
chr1:15705751
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.61-10486C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15705751 | ||||||
chr1:15706003
|
C | T | 1 | a0001c0001t0002g0309 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.61-10234C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706003 | ||||||
chr1:15706036
|
G | A | 6 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-10201G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706036 | ||||||
chr1:15706087
|
C | T | 2 | a0002c0002t0006g0113a0002c0002t0006g0114 | 2 | HG01243.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.61-10150C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706087 | ||||||
chr1:15706149
|
C | T | 1 | a0001c0004t0003g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.61-10088C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706149 | ||||||
chr1:15706225
|
G | A | 10 | a0002c0006t0004g0006a0002c0006t0004g0032a0002c0006t0004g0033others(7): Show | 11 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10012G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706225 | ||||||
chr1:15706392
|
A | ATTTG | 53 | a0001c0001t0017g0311a0002c0002t0006g0111a0002c0002t0006g0113others(50): Show | 56 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.61-9833_61-9830dup others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15706392 | |||||
chr1:15706467
|
ACGATCTC others(19): Show |
A | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-9768_61-9743del others(26): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15706467 | |||||
chr1:15706504
|
C | G | 7 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(4): Show | 8 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-9733C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706504 | ||||||
chr1:15706595
|
C | T | 2 | a0001c0024t0002g0220a0007c0025t0002g0163 | 2 | HG02698.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.61-9642C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706595 | ||||||
chr1:15706735
|
C | A | 1 | a0002c0005t0001g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.61-9502C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706735 | ||||||
chr1:15706764
|
T | C | 1 | a0001c0001t0002g0288 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.61-9473T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706764 | ||||||
chr1:15706839
|
G | A | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61-9398G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706839 | ||||||
chr1:15706911
|
T | C | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.61-9326T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706911 | ||||||
chr1:15706924
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.61-9313C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706924 | ||||||
chr1:15706952
|
A | G | 2 | a0002c0006t0004g0085a0002c0006t0004g0091 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.61-9285A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15706952 | ||||||
chr1:15707015
|
C | T | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-9222C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707015 | ||||||
chr1:15707025
|
C | T | 1 | a0003c0019t0004g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.61-9212C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707025 | ||||||
chr1:15707091
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.61-9146A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707091 | ||||||
chr1:15707104
|
CA | C | 102 | a0001c0001t0007g0127a0002c0002t0003g0001a0002c0002t0003g0007others(99): Show | 110 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.61-9121delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15707104 | |||||
chr1:15707104
|
CAA | C | 11 | a0002c0002t0003g0048a0002c0002t0008g0005a0002c0002t0008g0028others(8): Show | 12 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-9122_61-9121del others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15707104 | |||||
chr1:15707188
|
A | G | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.61-9049A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707188 | ||||||
chr1:15707268
|
A | AC | 6 | a0002c0002t0006g0104a0002c0002t0006g0106a0002c0002t0006g0107others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-8968dupC | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15707268 | |||||
chr1:15707269
|
C | CA | 95 | a0001c0001t0001g0174a0001c0024t0002g0220a0002c0002t0003g0001others(92): Show | 104 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.61-8954dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15707269 | |||||
chr1:15707269
|
C | CAA | 9 | a0002c0002t0008g0028a0002c0003t0001g0121a0002c0003t0003g0116others(6): Show | 9 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-8955_61-8954dup others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15707269 | |||||
chr1:15707358
|
G | A | 22 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(19): Show | 24 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.61-8879G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707358 | ||||||
chr1:15707706
|
T | A | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.61-8531T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707706 | ||||||
chr1:15707873
|
G | C | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.61-8364G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707873 | ||||||
chr1:15707999
|
C | G | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.61-8238C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15707999 | ||||||
chr1:15708175
|
G | A | 32 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(29): Show | 34 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.61-8062G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708175 | ||||||
chr1:15708248
|
C | T | 2 | a0002c0002t0010g0100a0002c0014t0004g0036 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.61-7989C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708248 | ||||||
chr1:15708249
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.61-7988G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708249 | ||||||
chr1:15708279
|
C | T | 1 | a0002c0003t0010g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61-7958C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708279 | ||||||
chr1:15708440
|
C | T | 5 | a0002c0006t0004g0006a0002c0006t0004g0032a0002c0006t0004g0033others(2): Show | 6 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-7797C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708440 | ||||||
chr1:15708506
|
T | C | 42 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(39): Show | 45 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.61-7731T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708506 | ||||||
chr1:15708510
|
C | T | 1 | a0002c0003t0008g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.61-7727C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708510 | ||||||
chr1:15708513
|
T | C | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.61-7724T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708513 | ||||||
chr1:15708515
|
C | T | 43 | a0001c0001t0002g0269a0002c0002t0008g0005a0002c0002t0008g0028others(40): Show | 46 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.61-7722C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708515 | ||||||
chr1:15708751
|
G | A | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.61-7486G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708751 | ||||||
chr1:15708785
|
A | C | 1 | a0001c0001t0002g0153 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.61-7452A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708785 | ||||||
chr1:15708878
|
A | G | 1 | a0002c0002t0003g0066 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61-7359A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708878 | ||||||
chr1:15708939
|
A | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0228a0001c0001t0002g0290 | 3 | HG00140.hp2 HG00741.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.61-7298A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708939 | ||||||
chr1:15708997
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.61-7240C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15708997 | ||||||
chr1:15709006
|
A | G | 9 | a0001c0001t0002g0021a0001c0001t0002g0130a0001c0001t0002g0223others(6): Show | 10 | HG02145.hp1 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-7231A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15709006 | ||||||
chr1:15709022
|
T | A | 3 | a0002c0002t0008g0005a0002c0002t0011g0004a0002c0002t0011g0005 | 4 | HG03540.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-7215T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15709022 | ||||||
chr1:15709025
|
C | T | 1 | a0001c0001t0002g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.61-7212C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15709025 | ||||||
chr1:15709320
|
G | A | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61-6917G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15709320 | ||||||
chr1:15709338
|
A | G | 1 | a0001c0001t0002g0289 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.61-6899A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15709338 | ||||||
chr1:15709397
|
A | G | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.61-6840A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15709397 | ||||||
chr1:15709531
|
G | A | 1 | a0002c0003t0020g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.61-6706G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15709531 | ||||||
chr1:15709780
|
ATG | A | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-6454_61-6453del others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15709780 | |||||
chr1:15710063
|
A | G | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-6174A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710063 | ||||||
chr1:15710095
|
C | T | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-6142C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710095 | ||||||
chr1:15710099
|
C | T | 3 | a0002c0009t0003g0072a0002c0009t0003g0073a0002c0009t0003g0078 | 3 | HG03490.hp1 HG03492.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.61-6138C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710099 | ||||||
chr1:15710192
|
C | A | 36 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(33): Show | 38 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.61-6045C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710192 | ||||||
chr1:15710227
|
C | CA | 11 | a0001c0001t0001g0166a0001c0001t0001g0175a0001c0001t0001g0226others(8): Show | 11 | HG01167.hp1 HG01261.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-5992dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15710227 | |||||
chr1:15710227
|
CA | C | 15 | a0001c0001t0002g0124a0001c0001t0002g0295a0001c0001t0007g0127others(12): Show | 16 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-5992delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15710227 | |||||
chr1:15710227
|
CAA | C | 15 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(12): Show | 16 | HG01891.hp1 HG02257.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.61-5993_61-5992del others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15710227 | |||||
chr1:15710247
|
T | C | 10 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(7): Show | 10 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.61-5990T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710247 | ||||||
chr1:15710295
|
T | C | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-5942T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710295 | ||||||
chr1:15710754
|
G | T | 36 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(33): Show | 38 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.61-5483G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710754 | ||||||
chr1:15710768
|
A | G | 36 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(33): Show | 38 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.61-5469A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710768 | ||||||
chr1:15710787
|
G | A | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.61-5450G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710787 | ||||||
chr1:15710917
|
G | A | 12 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0201others(9): Show | 12 | HG00099.hp1 HG00642.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-5320G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15710917 | ||||||
chr1:15711092
|
C | T | 3 | a0002c0002t0012g0026a0002c0002t0012g0027a0003c0015t0012g0025 | 3 | HG01891.hp1 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.61-5145C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711092 | ||||||
chr1:15711093
|
G | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0293a0001c0001t0002g0295others(2): Show | 6 | HG02258.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-5144G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711093 | ||||||
chr1:15711206
|
AAAAAT | A | 66 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(63): Show | 72 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.61-5017_61-5013del others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15711206 | |||||
chr1:15711313
|
A | T | 1 | a0002c0014t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.61-4924A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711313 | ||||||
chr1:15711330
|
T | C | 22 | a0002c0003t0003g0087a0002c0003t0004g0011a0002c0003t0004g0093others(19): Show | 24 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.61-4907T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711330 | ||||||
chr1:15711341
|
C | T | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-4896C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711341 | ||||||
chr1:15711448
|
T | A | 1 | a0002c0002t0006g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.61-4789T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711448 | ||||||
chr1:15711507
|
C | T | 2 | a0002c0002t0010g0100a0002c0014t0004g0036 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.61-4730C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711507 | ||||||
chr1:15711603
|
C | T | 66 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(63): Show | 72 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.61-4634C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711603 | ||||||
chr1:15711609
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.61-4628T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711609 | ||||||
chr1:15711629
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.61-4608G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711629 | ||||||
chr1:15711630
|
A | G | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.61-4607A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711630 | ||||||
chr1:15711796
|
A | G | 10 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(7): Show | 11 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-4441A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711796 | ||||||
chr1:15711831
|
T | C | 76 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(73): Show | 83 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.61-4406T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711831 | ||||||
chr1:15711885
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.61-4352G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711885 | ||||||
chr1:15711889
|
C | T | 3 | a0001c0001t0002g0199a0001c0001t0002g0209a0002c0003t0020g0024 | 3 | HG00323.hp2 HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.61-4348C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711889 | ||||||
chr1:15711950
|
C | G | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-4287C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711950 | ||||||
chr1:15711988
|
C | T | 1 | a0002c0006t0004g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.61-4249C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15711988 | ||||||
chr1:15712037
|
A | G | 76 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(73): Show | 83 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.61-4200A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712037 | ||||||
chr1:15712060
|
G | A | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61-4177G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712060 | ||||||
chr1:15712074
|
C | T | 2 | a0001c0001t0001g0215a0002c0002t0003g0051 | 2 | HG02970.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.61-4163C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712074 | ||||||
chr1:15712118
|
C | CA | 44 | a0001c0001t0001g0176a0001c0001t0001g0214a0001c0001t0001g0239others(41): Show | 46 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.61-4098dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15712118 | |||||
chr1:15712118
|
CA | C | 18 | a0001c0001t0001g0165a0001c0001t0001g0190a0001c0001t0001g0215others(15): Show | 19 | HG01070.hp1 HG01891.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.61-4098delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15712118 | |||||
chr1:15712184
|
G | A | 1 | a0001c0001t0002g0300 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.61-4053G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712184 | ||||||
chr1:15712198
|
A | T | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.61-4039A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712198 | ||||||
chr1:15712319
|
A | C | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-3918A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712319 | ||||||
chr1:15712341
|
G | A | 76 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(73): Show | 83 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.61-3896G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712341 | ||||||
chr1:15712384
|
C | G | 76 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(73): Show | 83 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.61-3853C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712384 | ||||||
chr1:15712440
|
C | T | 1 | a0002c0002t0003g0077 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.61-3797C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712440 | ||||||
chr1:15712486
|
C | G | 5 | a0001c0001t0002g0021a0001c0001t0002g0293a0001c0001t0002g0295others(2): Show | 6 | HG02258.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-3751C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712486 | ||||||
chr1:15712562
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.61-3675G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712562 | ||||||
chr1:15712648
|
C | CT | 27 | a0001c0001t0001g0174a0001c0001t0001g0189a0001c0001t0001g0198others(24): Show | 28 | HG00408.hp2 HG00438.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.61-3572dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15712648 | |||||
chr1:15712734
|
G | T | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.61-3503G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712734 | ||||||
chr1:15712758
|
A | AC | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(311): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.61-3476dupC | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15712758 | |||||
chr1:15712839
|
C | T | 2 | a0002c0007t0001g0095a0002c0007t0001g0112 | 2 | HG00323.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.61-3398C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712839 | ||||||
chr1:15712845
|
T | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(210): Show | 228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.61-3392T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15712845 | ||||||
chr1:15713244
|
A | G | 60 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(57): Show | 66 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-2993A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15713244 | ||||||
chr1:15713630
|
G | GT | 29 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(26): Show | 31 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.61-2604dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15713630 | |||||
chr1:15713630
|
G | T | 33 | a0002c0002t0003g0001a0002c0002t0003g0009a0002c0002t0003g0061others(30): Show | 38 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.61-2607G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15713630 | ||||||
chr1:15713634
|
G | T | 110 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(107): Show | 119 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.61-2603G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15713634 | ||||||
chr1:15713637
|
T | G | 2 | a0002c0002t0006g0106a0002c0002t0006g0107 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.61-2600T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15713637 | ||||||
chr1:15713705
|
A | G | 76 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(73): Show | 83 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.61-2532A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15713705 | ||||||
chr1:15713830
|
G | A | 1 | a0002c0002t0003g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.61-2407G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15713830 | ||||||
chr1:15713838
|
C | T | 5 | a0001c0001t0002g0133a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG01243.hp1 HG01358.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.61-2399C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15713838 | ||||||
chr1:15713941
|
G | GT | 19 | a0001c0001t0001g0151a0001c0001t0001g0213a0001c0001t0001g0214others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-2279dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15713941 | |||||
chr1:15713941
|
GT | G | 18 | a0001c0001t0001g0147a0001c0001t0002g0125a0001c0001t0002g0134others(15): Show | 19 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-2279delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15713941 | |||||
chr1:15714010
|
C | T | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-2227C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714010 | ||||||
chr1:15714087
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0129a0001c0001t0001g0176others(11): Show | 14 | HG00423.hp2 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-2150G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714087 | ||||||
chr1:15714108
|
G | A | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.61-2129G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714108 | ||||||
chr1:15714111
|
G | T | 75 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(72): Show | 82 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.61-2126G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714111 | ||||||
chr1:15714186
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.61-2051C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714186 | ||||||
chr1:15714348
|
T | TA | 90 | a0001c0001t0001g0172a0001c0001t0001g0274a0002c0002t0003g0001others(87): Show | 98 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.61-1868dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15714348 | |||||
chr1:15714348
|
TA | T | 11 | a0001c0001t0001g0131a0001c0001t0001g0166a0001c0001t0001g0226others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1868delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15714348 | |||||
chr1:15714388
|
C | T | 8 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0190others(5): Show | 8 | HG02071.hp2 HG02074.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-1849C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714388 | ||||||
chr1:15714651
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0151 | 2 | HG00408.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.61-1586G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714651 | ||||||
chr1:15714664
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61-1573G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714664 | ||||||
chr1:15714693
|
G | A | 1 | a0002c0002t0006g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.61-1544G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714693 | ||||||
chr1:15714890
|
G | A | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-1347G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15714890 | ||||||
chr1:15715025
|
A | T | 2 | a0002c0002t0010g0100a0002c0014t0004g0036 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.61-1212A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715025 | ||||||
chr1:15715111
|
C | T | 75 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(72): Show | 82 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.61-1126C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715111 | ||||||
chr1:15715157
|
TCAAGAAG others(5): Show |
T | 31 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(28): Show | 33 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.61-1067_61-1056del others(12): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 15715157 | |||||
chr1:15715387
|
A | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0165a0001c0001t0001g0166others(14): Show | 18 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.61-850A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715387 | ||||||
chr1:15715409
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.61-828A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715409 | ||||||
chr1:15715533
|
C | T | 75 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(72): Show | 82 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.61-704C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715533 | ||||||
chr1:15715706
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.61-531G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715706 | ||||||
chr1:15715756
|
C | A | 75 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(72): Show | 82 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.61-481C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715756 | ||||||
chr1:15715775
|
C | A | 74 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(71): Show | 81 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.61-462C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715775 | ||||||
chr1:15715777
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.61-460A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715777 | ||||||
chr1:15715782
|
A | G | 74 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(71): Show | 81 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.61-455A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715782 | ||||||
chr1:15715803
|
G | A | 74 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(71): Show | 81 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.61-434G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715803 | ||||||
chr1:15715831
|
C | T | 74 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(71): Show | 81 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.61-406C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715831 | ||||||
chr1:15715834
|
T | G | 2 | a0001c0008t0002g0285a0001c0008t0002g0287 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.61-403T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715834 | ||||||
chr1:15715839
|
G | A | 1 | a0002c0003t0003g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.61-398G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715839 | ||||||
chr1:15715894
|
T | C | 75 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(72): Show | 82 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.61-343T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15715894 | ||||||
chr1:15716145
|
C | G | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61-92C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15716145 | ||||||
chr1:15716229
|
TC | T | 65 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(62): Show | 71 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(68): Show |
splice_region_variant&intron_variant | LOW | c.61-7delC | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 1/19 | chr1 | 15716229 | ||||||
chr1:15716373
|
G | A | 1 | a0002c0002t0003g0051 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.167+30G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 2/19 | chr1 | 15716373 | ||||||
chr1:15716394
|
G | A | 1 | a0002c0005t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.167+51G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 2/19 | chr1 | 15716394 | ||||||
chr1:15716646
|
G | A | 10 | a0002c0006t0004g0006a0002c0006t0004g0032a0002c0006t0004g0033others(7): Show | 11 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-61G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 2/19 | chr1 | 15716646 | ||||||
chr1:15716662
|
G | A | 75 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(72): Show | 82 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.168-45G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 2/19 | chr1 | 15716662 | ||||||
chr1:15717081
|
A | G | 1 | a0002c0003t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.277+265A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717081 | ||||||
chr1:15717174
|
C | T | 1 | a0002c0003t0008g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.277+358C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717174 | ||||||
chr1:15717258
|
T | G | 33 | a0002c0003t0001g0121a0002c0003t0003g0087a0002c0003t0003g0116others(30): Show | 35 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.277+442T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717258 | ||||||
chr1:15717297
|
C | T | 3 | a0001c0001t0002g0206a0001c0001t0002g0303a0005c0021t0002g0200 | 3 | HG01168.hp2 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.277+481C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717297 | ||||||
chr1:15717306
|
T | G | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+490T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717306 | ||||||
chr1:15717403
|
C | T | 65 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(62): Show | 71 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.278-490C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717403 | ||||||
chr1:15717484
|
A | G | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.278-409A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717484 | ||||||
chr1:15717522
|
AAG | A | 3 | a0002c0002t0012g0026a0002c0002t0012g0027a0003c0015t0012g0025 | 3 | HG01891.hp1 HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.278-368_278-367del others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 15717522 | |||||
chr1:15717558
|
G | A | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092 | 3 | HG00642.hp2 HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.278-335G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717558 | ||||||
chr1:15717650
|
G | A | 4 | a0002c0003t0003g0116a0002c0003t0003g0118a0002c0003t0003g0119others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-243G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717650 | ||||||
chr1:15717687
|
T | G | 2 | a0002c0006t0004g0085a0002c0006t0004g0091 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.278-206T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 3/19 | chr1 | 15717687 | ||||||
chr1:15718106
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.377+114C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 4/19 | chr1 | 15718106 | ||||||
chr1:15718290
|
A | C | 1 | a0001c0011t0001g0144 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.378-248A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 4/19 | chr1 | 15718290 | ||||||
chr1:15718312
|
C | G | 77 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(74): Show | 84 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(81): Show |
intron_variant | MODIFIER | c.378-226C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 4/19 | chr1 | 15718312 | ||||||
chr1:15718410
|
C | A | 1 | a0002c0002t0008g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.378-128C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 4/19 | chr1 | 15718410 | ||||||
chr1:15718434
|
A | G | 77 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(74): Show | 84 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(81): Show |
intron_variant | MODIFIER | c.378-104A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 4/19 | chr1 | 15718434 | ||||||
chr1:15718450
|
G | A | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.378-88G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 4/19 | chr1 | 15718450 | ||||||
chr1:15718679
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0015g0003a0001c0004t0003g0271 | 4 | HG01168.hp1 HG02683.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+54G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15718679 | ||||||
chr1:15718755
|
A | G | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.465+130A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15718755 | ||||||
chr1:15718766
|
T | C | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.465+141T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15718766 | ||||||
chr1:15718958
|
T | C | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.465+333T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15718958 | ||||||
chr1:15719041
|
C | G | 2 | a0002c0002t0010g0100a0002c0014t0004g0036 | 2 | HG01109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.465+416C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719041 | ||||||
chr1:15719084
|
A | G | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.465+459A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719084 | ||||||
chr1:15719219
|
G | A | 2 | a0001c0001t0001g0193a0001c0004t0014g0194 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.466-515G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719219 | ||||||
chr1:15719278
|
C | T | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.466-456C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719278 | ||||||
chr1:15719279
|
G | A | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.466-455G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719279 | ||||||
chr1:15719303
|
T | C | 1 | a0002c0005t0001g0055 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.466-431T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719303 | ||||||
chr1:15719408
|
G | A | 2 | a0001c0001t0002g0199a0001c0001t0002g0209 | 2 | HG00323.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.466-326G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719408 | ||||||
chr1:15719444
|
C | CT | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.466-289dupT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 15719444 | |||||
chr1:15719450
|
CAA | C | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.466-274_466-273del others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 15719450 | |||||
chr1:15719470
|
TAGAG | T | 8 | a0002c0003t0001g0121a0002c0003t0003g0116a0002c0003t0003g0118others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-252_466-249del others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 15719470 | |||||
chr1:15719614
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(218): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.466-120C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | chr1 | 15719614 | ||||||
chr1:15719632
|
CAA | C | 2 | a0002c0002t0003g0009a0002c0002t0003g0064 | 3 | HG01516.hp1 HG01517.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.466-100_466-99delA others(1): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 15719632 | |||||
chr1:15720057
|
T | G | 3 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0292 | 3 | HG01943.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.652+137T>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720057 | ||||||
chr1:15720090
|
G | A | 1 | a0001c0004t0005g0286 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.652+170G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720090 | ||||||
chr1:15720128
|
T | TTA | 8 | a0001c0001t0001g0151a0001c0001t0001g0214a0001c0001t0001g0274others(5): Show | 8 | HG00544.hp2 HG01192.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.652+229_652+230dup others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720128 | |||||
chr1:15720128
|
T | TTATA | 27 | a0002c0002t0003g0007a0002c0002t0003g0039a0002c0002t0003g0041others(24): Show | 28 | HG00639.hp2 HG01099.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.652+227_652+230dup others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720128 | |||||
chr1:15720128
|
T | TTATATA | 19 | a0002c0002t0003g0047a0002c0002t0003g0048a0002c0002t0003g0050others(16): Show | 20 | HG01109.hp1 HG01255.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.652+225_652+230dup others(6): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720128 | |||||
chr1:15720128
|
T | TTATATAT others(5): Show |
1 | a0002c0002t0003g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.652+219_652+230dup others(12): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720128 | |||||
chr1:15720128
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.652+217_652+230dup others(14): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720128 | |||||
chr1:15720128
|
TTA | T | 31 | a0001c0001t0002g0124a0002c0002t0008g0005a0002c0002t0008g0030others(28): Show | 33 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.652+229_652+230del others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720128 | |||||
chr1:15720129
|
T | TATATAA | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+214_652+215ins others(6): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720129 | |||||
chr1:15720149
|
T | A | 46 | a0002c0002t0006g0111a0002c0002t0006g0113a0002c0002t0006g0114others(43): Show | 49 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.652+229T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720149 | ||||||
chr1:15720149
|
T | TAA | 4 | a0002c0002t0003g0009a0002c0002t0003g0061a0002c0002t0003g0065others(1): Show | 5 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.652+232_652+233dup others(2): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720149 | |||||
chr1:15720149
|
T | TATAA | 6 | a0002c0002t0003g0083a0002c0002t0004g0010a0002c0002t0004g0043others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.652+230_652+231ins others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720149 | |||||
chr1:15720149
|
T | TATATATA others(1): Show |
2 | a0002c0002t0003g0001a0002c0002t0003g0084 | 4 | HG01167.hp2 HG02280.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.652+230_652+231ins others(8): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720149 | |||||
chr1:15720151
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.652+231A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720151 | ||||||
chr1:15720159
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.652+239A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720159 | ||||||
chr1:15720425
|
C | T | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.652+505C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720425 | ||||||
chr1:15720577
|
AT | A | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.652+661delT | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 15720577 | |||||
chr1:15720698
|
C | T | 1 | a0003c0019t0004g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.653-631C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720698 | ||||||
chr1:15720834
|
A | T | 159 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0138others(156): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.653-495A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15720834 | ||||||
chr1:15721058
|
T | C | 1 | a0002c0002t0003g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.653-271T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15721058 | ||||||
chr1:15721231
|
T | C | 112 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(109): Show | 121 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(118): Show |
intron_variant | MODIFIER | c.653-98T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15721231 | ||||||
chr1:15721259
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.653-70C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15721259 | ||||||
chr1:15721292
|
T | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0131a0001c0001t0001g0142others(4): Show | 8 | HG00423.hp1 HG02129.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.653-37T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 6/19 | chr1 | 15721292 | ||||||
chr1:15721475
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0265 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.712+87T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721475 | ||||||
chr1:15721510
|
A | G | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.712+122A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721510 | ||||||
chr1:15721524
|
A | G | 1 | a0012c0018t0008g0102 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.712+136A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721524 | ||||||
chr1:15721543
|
T | C | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.712+155T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721543 | ||||||
chr1:15721619
|
C | T | 41 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(38): Show | 44 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.712+231C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721619 | ||||||
chr1:15721644
|
G | A | 1 | a0001c0001t0002g0307 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.712+256G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721644 | ||||||
chr1:15721644
|
G | C | 7 | a0002c0002t0006g0104a0002c0002t0006g0106a0002c0002t0006g0107others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.712+256G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721644 | ||||||
chr1:15721692
|
C | T | 2 | a0001c0001t0002g0202a0001c0001t0002g0218 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.712+304C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721692 | ||||||
chr1:15721696
|
G | C | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.712+308G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721696 | ||||||
chr1:15721709
|
G | A | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+321G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15721709 | ||||||
chr1:15722014
|
A | G | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+626A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722014 | ||||||
chr1:15722142
|
GTTATT | G | 2 | a0002c0003t0004g0011a0002c0003t0004g0093 | 3 | HG01070.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.712+763_712+767del others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15722142 | |||||
chr1:15722167
|
G | A | 113 | a0001c0001t0017g0311a0002c0002t0003g0001a0002c0002t0003g0007others(110): Show | 122 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.712+779G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722167 | ||||||
chr1:15722274
|
G | A | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.712+886G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722274 | ||||||
chr1:15722298
|
C | T | 1 | a0002c0003t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.712+910C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722298 | ||||||
chr1:15722300
|
C | T | 1 | a0002c0002t0003g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.712+912C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722300 | ||||||
chr1:15722307
|
C | A | 1 | a0002c0003t0019g0115 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712+919C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722307 | ||||||
chr1:15722362
|
T | C | 1 | a0001c0004t0003g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.712+974T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722362 | ||||||
chr1:15722456
|
A | T | 108 | a0002c0002t0003g0001a0002c0002t0003g0007a0002c0002t0003g0009others(105): Show | 117 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(114): Show |
intron_variant | MODIFIER | c.712+1068A>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722456 | ||||||
chr1:15722490
|
G | T | 1 | a0002c0005t0001g0037 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.712+1102G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722490 | ||||||
chr1:15722705
|
C | T | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+1317C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722705 | ||||||
chr1:15722790
|
C | G | 67 | a0001c0001t0002g0307a0001c0004t0005g0308a0002c0002t0003g0001others(64): Show | 73 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.712+1402C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722790 | ||||||
chr1:15722845
|
G | A | 41 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(38): Show | 44 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.712+1457G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722845 | ||||||
chr1:15722933
|
C | T | 2 | a0001c0001t0002g0203a0001c0001t0002g0204 | 2 | NA18948.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.712+1545C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15722933 | ||||||
chr1:15723098
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.712+1710A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723098 | ||||||
chr1:15723369
|
G | T | 4 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092others(1): Show | 4 | HG00642.hp2 HG01099.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-1948G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723369 | ||||||
chr1:15723398
|
C | T | 109 | a0001c0001t0002g0307a0001c0004t0005g0308a0002c0002t0003g0001others(106): Show | 118 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(115): Show |
intron_variant | MODIFIER | c.713-1919C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723398 | ||||||
chr1:15723449
|
T | TA | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(106): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.713-1853dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15723449 | |||||
chr1:15723449
|
TA | T | 13 | a0001c0001t0002g0138a0001c0001t0002g0262a0001c0001t0002g0289others(10): Show | 16 | HG01069.hp1 HG01167.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.713-1853delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15723449 | |||||
chr1:15723464
|
A | G | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.713-1853A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723464 | ||||||
chr1:15723572
|
T | C | 1 | a0003c0015t0012g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.713-1745T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723572 | ||||||
chr1:15723724
|
G | A | 1 | a0002c0002t0006g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.713-1593G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723724 | ||||||
chr1:15723731
|
C | T | 1 | a0002c0002t0003g0077 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.713-1586C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723731 | ||||||
chr1:15723744
|
C | CA | 20 | a0001c0001t0001g0129a0001c0001t0001g0155a0001c0001t0001g0170others(17): Show | 20 | HG00140.hp1 HG00438.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.713-1548dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15723744 | |||||
chr1:15723744
|
CA | C | 9 | a0001c0001t0002g0277a0001c0001t0002g0300a0001c0001t0007g0127others(6): Show | 9 | HG00642.hp2 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.713-1548delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15723744 | |||||
chr1:15723744
|
CAA | C | 50 | a0002c0002t0003g0057a0002c0002t0003g0067a0002c0002t0003g0079others(47): Show | 53 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.713-1549_713-1548d others(4): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15723744 | |||||
chr1:15723744
|
CAAA | C | 56 | a0001c0001t0002g0307a0001c0004t0005g0308a0002c0002t0003g0001others(53): Show | 62 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.713-1550_713-1548d others(5): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15723744 | |||||
chr1:15723882
|
C | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0155 | 2 | NA18966.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.713-1435C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723882 | ||||||
chr1:15723932
|
ACCAGCCA others(9): Show |
A | 1 | a0002c0003t0008g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.713-1381_713-1366d others(18): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15723932 | |||||
chr1:15723975
|
A | C | 72 | a0001c0001t0002g0232a0001c0001t0002g0245a0001c0001t0002g0305others(69): Show | 78 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.713-1342A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723975 | ||||||
chr1:15723994
|
T | A | 7 | a0002c0002t0008g0005a0002c0002t0008g0028a0002c0002t0008g0030others(4): Show | 8 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.713-1323T>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15723994 | ||||||
chr1:15724026
|
G | A | 52 | a0001c0001t0017g0311a0002c0002t0006g0111a0002c0002t0006g0113others(49): Show | 55 | HG00323.hp1 HG00642.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.713-1291G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724026 | ||||||
chr1:15724101
|
G | A | 1 | a0002c0007t0001g0088 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.713-1216G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724101 | ||||||
chr1:15724206
|
C | T | 1 | a0002c0006t0004g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.713-1111C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724206 | ||||||
chr1:15724310
|
C | T | 1 | a0002c0003t0020g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.713-1007C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724310 | ||||||
chr1:15724418
|
G | C | 9 | a0002c0002t0008g0005a0002c0002t0008g0030a0002c0002t0011g0004others(6): Show | 10 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.713-899G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724418 | ||||||
chr1:15724448
|
G | A | 7 | a0001c0001t0017g0311a0001c0004t0005g0279a0002c0003t0008g0022others(4): Show | 7 | HG00642.hp2 HG01099.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.713-869G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724448 | ||||||
chr1:15724481
|
C | CA | 7 | a0001c0001t0002g0208a0001c0001t0002g0252a0002c0002t0006g0106others(4): Show | 7 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.713-821dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 15724481 | |||||
chr1:15724515
|
A | G | 2 | a0002c0005t0001g0037a0011c0013t0001g0103 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.713-802A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724515 | ||||||
chr1:15724555
|
A | G | 1 | a0001c0001t0002g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.713-762A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724555 | ||||||
chr1:15724607
|
G | A | 1 | a0002c0010t0003g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.713-710G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724607 | ||||||
chr1:15724672
|
C | G | 2 | a0002c0002t0003g0009a0002c0002t0003g0064 | 3 | HG01516.hp1 HG01517.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.713-645C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724672 | ||||||
chr1:15724765
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(97): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.713-552T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724765 | ||||||
chr1:15724854
|
C | A | 20 | a0001c0001t0001g0185a0001c0001t0002g0013a0001c0001t0002g0159others(17): Show | 21 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.713-463C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724854 | ||||||
chr1:15724878
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.713-439C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724878 | ||||||
chr1:15724903
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.713-414G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15724903 | ||||||
chr1:15725052
|
G | C | 20 | a0001c0001t0002g0234a0001c0001t0002g0293a0001c0001t0002g0295others(17): Show | 21 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.713-265G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15725052 | ||||||
chr1:15725089
|
C | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(282): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.713-228C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15725089 | ||||||
chr1:15725250
|
A | G | 3 | a0001c0001t0002g0307a0002c0002t0004g0010a0002c0002t0004g0043 | 4 | HG01069.hp2 HG01071.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.713-67A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15725250 | ||||||
chr1:15725252
|
G | A | 7 | a0002c0006t0004g0006a0002c0006t0004g0032a0002c0006t0004g0033others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.713-65G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15725252 | ||||||
chr1:15725272
|
C | T | 12 | a0001c0001t0002g0253a0002c0002t0006g0113a0002c0002t0006g0114others(9): Show | 12 | HG00323.hp1 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.713-45C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 7/19 | chr1 | 15725272 | ||||||
chr1:15725785
|
T | C | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092 | 3 | HG00642.hp2 HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.941+240T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15725785 | ||||||
chr1:15725838
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.941+293C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15725838 | ||||||
chr1:15725847
|
G | A | 11 | a0001c0004t0005g0308a0002c0002t0006g0104a0002c0002t0006g0106others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.941+302G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15725847 | ||||||
chr1:15725911
|
G | A | 1 | a0002c0003t0020g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.941+366G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15725911 | ||||||
chr1:15725991
|
C | G | 1 | a0001c0004t0005g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.941+446C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15725991 | ||||||
chr1:15725999
|
G | T | 2 | a0001c0001t0002g0211a0001c0001t0002g0275 | 2 | NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.941+454G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15725999 | ||||||
chr1:15726091
|
G | A | 4 | a0002c0002t0012g0026a0002c0002t0012g0027a0002c0003t0004g0011others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.941+546G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726091 | ||||||
chr1:15726293
|
A | G | 8 | a0002c0002t0008g0005a0002c0002t0008g0030a0002c0002t0010g0100others(5): Show | 9 | HG01109.hp2 HG02976.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.942-721A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726293 | ||||||
chr1:15726346
|
A | G | 11 | a0001c0004t0005g0308a0002c0002t0006g0104a0002c0002t0006g0106others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.942-668A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726346 | ||||||
chr1:15726415
|
G | T | 2 | a0002c0003t0004g0011a0002c0003t0004g0093 | 3 | HG01070.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.942-599G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726415 | ||||||
chr1:15726416
|
C | T | 1 | a0002c0003t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.942-598C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726416 | ||||||
chr1:15726518
|
C | T | 3 | a0002c0003t0008g0022a0002c0003t0008g0023a0002c0003t0010g0092 | 3 | HG00642.hp2 HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.942-496C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726518 | ||||||
chr1:15726570
|
C | T | 2 | a0002c0002t0003g0082a0002c0012t0003g0049 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.942-444C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726570 | ||||||
chr1:15726571
|
G | A | 11 | a0001c0004t0005g0308a0002c0002t0006g0104a0002c0002t0006g0106others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.942-443G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726571 | ||||||
chr1:15726593
|
C | G | 1 | a0002c0002t0003g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.942-421C>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726593 | ||||||
chr1:15726763
|
T | C | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.942-251T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726763 | ||||||
chr1:15726764
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.942-250C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726764 | ||||||
chr1:15726924
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.942-90A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726924 | ||||||
chr1:15726998
|
G | A | 82 | a0001c0001t0002g0251a0001c0001t0017g0311a0001c0004t0003g0015others(79): Show | 90 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.942-16G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15726998 | ||||||
chr1:15727011
|
C | T | 2 | a0002c0002t0006g0113a0002c0002t0006g0114 | 2 | HG01243.hp2 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.942-3C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 8/19 | chr1 | 15727011 | ||||||
chr1:15728021
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1761-58G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 9/19 | chr1 | 15728021 | ||||||
chr1:15728197
|
G | A | 1 | a0002c0002t0008g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1830+49G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 10/19 | chr1 | 15728197 | ||||||
chr1:15728210
|
G | A | 2 | a0012c0018t0008g0102a0014c0016t0008g0101 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1831-57G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 10/19 | chr1 | 15728210 | ||||||
chr1:15728523
|
G | C | 1 | a0001c0004t0005g0308 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1922-146G>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 11/19 | chr1 | 15728523 | ||||||
chr1:15728539
|
C | T | 1 | a0002c0005t0001g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1922-130C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 11/19 | chr1 | 15728539 | ||||||
chr1:15728544
|
C | T | 53 | a0001c0001t0005g0246a0001c0004t0003g0186a0001c0004t0003g0196others(50): Show | 55 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1922-125C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 11/19 | chr1 | 15728544 | ||||||
chr1:15728558
|
T | C | 7 | a0002c0002t0006g0111a0002c0002t0006g0113a0002c0002t0006g0114others(4): Show | 7 | HG00642.hp2 HG01099.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1922-111T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 11/19 | chr1 | 15728558 | ||||||
chr1:15728852
|
A | C | 1 | a0002c0002t0003g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1986+119A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 12/19 | chr1 | 15728852 | ||||||
chr1:15729051
|
G | A | 1 | a0002c0002t0003g0057 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1987-51G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 12/19 | chr1 | 15729051 | ||||||
chr1:15729051
|
G | T | 1 | a0002c0003t0010g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1987-51G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 12/19 | chr1 | 15729051 | ||||||
chr1:15729237
|
C | T | 107 | a0001c0001t0005g0246a0001c0001t0017g0311a0001c0004t0003g0015others(104): Show | 117 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(114): Show |
intron_variant | MODIFIER | c.2075+47C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 13/19 | chr1 | 15729237 | ||||||
chr1:15729436
|
T | C | 107 | a0001c0001t0005g0246a0001c0001t0017g0311a0001c0004t0003g0015others(104): Show | 117 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(114): Show |
intron_variant | MODIFIER | c.2075+246T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 13/19 | chr1 | 15729436 | ||||||
chr1:15729532
|
C | T | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2076-265C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 13/19 | chr1 | 15729532 | ||||||
chr1:15729533
|
C | T | 1 | a0002c0002t0008g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2076-264C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 13/19 | chr1 | 15729533 | ||||||
chr1:15729576
|
A | C | 1 | a0002c0002t0003g0058 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2076-221A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 13/19 | chr1 | 15729576 | ||||||
chr1:15729984
|
C | T | 7 | a0002c0002t0008g0005a0002c0002t0008g0030a0002c0002t0010g0100others(4): Show | 8 | HG01109.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2208+55C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15729984 | ||||||
chr1:15730046
|
TGGGCG | T | 23 | a0001c0001t0001g0152a0001c0001t0002g0207a0001c0001t0002g0208others(20): Show | 25 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2208+147_2208+151d others(7): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 15730046 | |||||
chr1:15730046
|
TGGGCGGG others(3): Show |
T | 2 | a0001c0004t0005g0279a0002c0003t0003g0087 | 2 | HG01106.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2208+142_2208+151d others(12): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 15730046 | |||||
chr1:15730046
|
TGGGCGGG others(8): Show |
T | 86 | a0001c0001t0005g0246a0001c0004t0003g0015a0001c0004t0003g0186others(83): Show | 94 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.2208+137_2208+151d others(17): Show |
PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 15730046 | |||||
chr1:15730070
|
C | T | 5 | a0002c0002t0003g0001a0002c0002t0003g0083a0002c0002t0003g0084others(2): Show | 7 | HG01167.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2208+141C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730070 | ||||||
chr1:15730127
|
G | T | 9 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0149others(6): Show | 9 | HG01123.hp1 HG01192.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.2208+198G>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730127 | ||||||
chr1:15730179
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2208+250G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730179 | ||||||
chr1:15730245
|
C | A | 75 | a0001c0001t0005g0246a0001c0004t0003g0186a0001c0004t0003g0196others(72): Show | 81 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.2209-287C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730245 | ||||||
chr1:15730421
|
G | A | 2 | a0003c0015t0012g0025a0003c0019t0004g0123 | 2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2209-111G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730421 | ||||||
chr1:15730447
|
G | GA | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(183): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.2209-76dupA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 15730447 | |||||
chr1:15730454
|
A | C | 2 | a0002c0006t0004g0085a0002c0006t0004g0091 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2209-78A>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730454 | ||||||
chr1:15730513
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2209-19G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730513 | ||||||
chr1:15730518
|
C | T | 1 | a0002c0002t0003g0057 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2209-14C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 14/19 | chr1 | 15730518 | ||||||
chr1:15730791
|
G | A | 1 | a0002c0003t0020g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2399+69G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 15/19 | chr1 | 15730791 | ||||||
chr1:15730984
|
G | A | 1 | a0014c0016t0008g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2400-208G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 15/19 | chr1 | 15730984 | ||||||
chr1:15731169
|
C | T | 1 | a0003c0015t0012g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2400-23C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 15/19 | chr1 | 15731169 | ||||||
chr1:15731305
|
G | A | 2 | a0002c0006t0004g0085a0002c0006t0004g0091 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2465+48G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 16/19 | chr1 | 15731305 | ||||||
chr1:15731444
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2465+187G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 16/19 | chr1 | 15731444 | ||||||
chr1:15731708
|
T | C | 6 | a0002c0002t0006g0104a0002c0002t0006g0106a0002c0002t0006g0107others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2466-181T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 16/19 | chr1 | 15731708 | ||||||
chr1:15732105
|
AG | A | 6 | a0002c0002t0006g0104a0002c0002t0006g0106a0002c0002t0006g0107others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2625+60delG | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 15732105 | |||||
chr1:15732154
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2625+106C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 17/19 | chr1 | 15732154 | ||||||
chr1:15732203
|
CA | C | 53 | a0001c0001t0005g0246a0001c0004t0003g0015a0001c0004t0003g0186others(50): Show | 57 | HG00280.hp1 HG00639.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.2626-146delA | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 17/19 | chr1 | 15732203 | ||||||
chr1:15732245
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2626-105C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 17/19 | chr1 | 15732245 | ||||||
chr1:15732548
|
C | T | 1 | a0002c0003t0020g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2805+19C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 18/19 | chr1 | 15732548 | ||||||
chr1:15732833
|
A | G | 6 | a0002c0002t0006g0104a0002c0002t0006g0106a0002c0002t0006g0107others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2922+105A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15732833 | ||||||
chr1:15732938
|
G | A | 1 | a0011c0013t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2922+210G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15732938 | ||||||
chr1:15732960
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2922+232G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15732960 | ||||||
chr1:15732969
|
G | A | 1 | a0001c0001t0017g0311 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2922+241G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15732969 | ||||||
chr1:15733039
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2922+311G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733039 | ||||||
chr1:15733063
|
C | T | 30 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0240others(27): Show | 32 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.2922+335C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733063 | ||||||
chr1:15733199
|
C | T | 21 | a0002c0002t0004g0010a0002c0002t0004g0043a0002c0002t0012g0026others(18): Show | 24 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.2922+471C>T | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733199 | ||||||
chr1:15733213
|
C | A | 1 | a0001c0001t0007g0259 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2922+485C>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733213 | ||||||
chr1:15733233
|
TC | T | 6 | a0001c0001t0005g0246a0001c0004t0005g0141a0001c0004t0005g0241others(3): Show | 6 | HG01496.hp2 HG01952.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.2922+508delC | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 15733233 | |||||
chr1:15733433
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0017g0311 | 2 | NA18989.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2923-364G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733433 | ||||||
chr1:15733483
|
A | G | 14 | a0001c0004t0005g0279a0002c0002t0003g0001a0002c0002t0003g0083others(11): Show | 16 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.2923-314A>G | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733483 | ||||||
chr1:15733630
|
G | A | 9 | a0002c0002t0008g0005a0002c0002t0008g0030a0002c0002t0010g0100others(6): Show | 10 | HG01109.hp2 HG02258.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2923-167G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733630 | ||||||
chr1:15733717
|
G | A | 1 | a0001c0001t0002g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2923-80G>A | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733717 | ||||||
chr1:15733775
|
T | C | 5 | a0002c0002t0012g0026a0002c0002t0012g0027a0002c0003t0004g0011others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.2923-22T>C | PLEKHM2 | ENSG00000116786.13 | transcript | ENST00000375799.8 | protein_coding | 19/19 | chr1 | 15733775 |