geneid | 9842 |
---|---|
ensemblid | ENSG00000225190.12 |
hgncid | 29017 |
symbol | PLEKHM1 |
name | pleckstrin homology and RUN domain containing M1 |
refseq_nuc | NM_014798.3 |
refseq_prot | NP_055613.1 |
ensembl_nuc | ENST00000430334.8 |
ensembl_prot | ENSP00000389913.3 |
mane_status | MANE Select |
chr | chr17 |
start | 45435900 |
end | 45490721 |
strand | - |
ver | v1.2 |
region | chr17:45435900-45490721 |
region5000 | chr17:45430900-45495721 |
regionname0 | PLEKHM1_chr17_45435900_45490721 |
regionname5000 | PLEKHM1_chr17_45430900_45495721 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1056 | 317 | 87 | 66 | 119 | 16 | 28 | 96 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0002 | 0/0 | 1056 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0003 | 0/0 | 1056 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0004 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0005 | 0/0 | 1056 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3171 | 284 | 75 | 57 | 116 | 12 | 23 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0002 | 0/0 | 3171 | 20 | 2 | 8 | 1 | 4 | 5 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0003 | 0/0 | 3171 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0004 | 0/0 | 3171 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0005 | 0/0 | 3171 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0006 | 0/0 | 3171 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0007 | 0/0 | 3171 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0008 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0009 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0010 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0011 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0012 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
c0013 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2070 | 265 | 77 | 49 | 115 | 7 | 16 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0002 | 0/0 | 2070 | 20 | 1 | 8 | 1 | 4 | 6 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0003 | 0/0 | 2070 | 17 | 0 | 6 | 1 | 4 | 6 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0004 | 0/0 | 2070 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0005 | 0/0 | 2070 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0006 | 0/0 | 2070 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0007 | 0/0 | 2070 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0008 | 0/0 | 2070 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0009 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0010 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0011 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0012 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0013 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0014 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0015 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
t0016 | 0/0 | 2070 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 1 | 3 | 5 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0003 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0004 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3171 | 284 | 75 | 57 | 116 | 12 | 23 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0002 | 0/0 | 3171 | 20 | 2 | 8 | 1 | 4 | 5 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0004 | 0/0 | 3171 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0005 | 0/0 | 3171 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0008 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0009 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0010 | 0/0 | 3171 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0011 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0013 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0002c0003 | 0/0 | 3171 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0003c0007 | 0/0 | 3171 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0004c0012 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0005c0006 | 0/0 | 3171 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5240 | 247 | 62 | 49 | 113 | 7 | 15 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0003 | 0/0 | 5240 | 15 | 0 | 5 | 0 | 4 | 6 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0004 | 0/0 | 5240 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0005 | 0/0 | 5240 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0006 | 0/0 | 5240 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0007 | 0/0 | 5240 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0008 | 0/0 | 5240 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0009 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0010 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0011 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0013 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0014 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0015 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0001t0016 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0002t0001 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0002t0002 | 0/0 | 5240 | 19 | 1 | 8 | 1 | 4 | 5 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0004t0001 | 0/0 | 5240 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0005t0001 | 0/0 | 5240 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0008t0001 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0009t0012 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0010t0003 | 0/0 | 5240 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0011t0003 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0001c0013t0001 | 0/0 | 5240 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0002c0003t0001 | 0/0 | 5240 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0003c0007t0001 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0004c0012t0001 | 0/0 | 5240 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
a0005c0006t0002 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | copy fasta | chr17 | 45430900 | 45495721 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 1 | 3 | 5 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0003 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0005g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0007g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0013g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0015g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0001t0016g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0009t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0010t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0011t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0001c0013t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0002c0003t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0002c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0003c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0004c0012t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
a0005c0006t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0016 | g0248 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0066 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0136 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00673 | hp2 | a0001 | c0001 | t0015 | g0209 | EAS | CHS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01099 | hp2 | a0001 | c0010 | t0003 | g0240 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0120 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0068 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0064 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | IBS | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0085 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0073 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0051 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02523 | hp1 | a0004 | c0012 | t0001 | g0182 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02602 | hp2 | a0005 | c0006 | t0002 | g0067 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02647 | hp1 | a0002 | c0003 | t0001 | g0044 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02647 | hp2 | a0001 | c0009 | t0012 | g0057 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0086 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0049 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0062 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02818 | hp1 | a0001 | c0004 | t0001 | g0050 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02896 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02922 | hp1 | a0001 | c0005 | t0001 | g0075 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0052 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0048 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03453 | hp1 | a0002 | c0003 | t0001 | g0008 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03540 | hp1 | a0001 | c0001 | t0014 | g0084 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03579 | hp1 | a0001 | c0005 | t0001 | g0247 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0036 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0063 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG04199 | hp2 | a0001 | c0001 | t0007 | g0036 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG04204 | hp2 | a0003 | c0007 | t0001 | g0079 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18942 | hp1 | a0001 | c0011 | t0003 | g0150 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18978 | hp1 | a0001 | c0008 | t0001 | g0198 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19005 | hp2 | a0001 | c0001 | t0013 | g0164 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19030 | hp2 | a0001 | c0005 | t0001 | g0246 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19080 | hp1 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | YRI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ASW | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0069 | EUR | TSI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0138 | EUR | TSI | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02559 | hp1 | a0001 | c0013 | t0001 | g0078 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0054 | AFR | MSL | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | USA | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0191 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0162 | REF | REF | PLEKHM1_chr17_45430900_45495721 | PLEKHM1 | chr17 | 45430900 | 45495721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45453891
|
C | T | 1 | a0003 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1961G>A | p.Cys654Tyr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/12 | 2072/5240 | 1961/3171 | 654/1056 | chr17 | 45453891 | ||
chr17:45458385
|
G | T | 1 | a0002 | 5 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.1363C>A | p.Pro455Thr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/12 | 1474/5240 | 1363/3171 | 455/1056 | chr17 | 45458385 | ||
chr17:45468456
|
G | A | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1061C>T | p.Ala354Val | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/12 | 1172/5240 | 1061/3171 | 354/1056 | chr17 | 45468456 | ||
chr17:45475377
|
G | A | 1 | a0005 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.646C>T | p.Arg216Trp | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 757/5240 | 646/3171 | 216/1056 | chr17 | 45475377 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45437960
|
C | T | 1 | a0001c0010 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.3069G>A | p.Glu1023Glu | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 3180/5240 | 3069/3171 | 1023/1056 | chr17 | 45437960 | ||
chr17:45437969
|
C | T | 1 | a0001c0005 | 3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
splice_region_variant&synonymous_variant | LOW | c.3060G>A | p.Arg1020Arg | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 3171/5240 | 3060/3171 | 1020/1056 | chr17 | 45437969 | ||
chr17:45439623
|
C | T | 2 | a0001c0004a0002c0003 | 10 | HG02257.hp2 HG02647.hp1 HG02717.hp2 others(7): Show |
synonymous_variant | LOW | c.2913G>A | p.Gly971Gly | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/12 | 3024/5240 | 2913/3171 | 971/1056 | chr17 | 45439623 | ||
chr17:45445543
|
G | T | 1 | a0001c0009 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.2764C>A | p.Arg922Arg | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/12 | 2875/5240 | 2764/3171 | 922/1056 | chr17 | 45445543 | ||
chr17:45453575
|
G | C | 1 | a0001c0011 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.2277C>G | p.Ala759Ala | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/12 | 2388/5240 | 2277/3171 | 759/1056 | chr17 | 45453575 | ||
chr17:45453857
|
C | T | 1 | a0001c0008 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.1995G>A | p.Ala665Ala | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/12 | 2106/5240 | 1995/3171 | 665/1056 | chr17 | 45453857 | ||
chr17:45468527
|
T | C | 3 | a0001c0002a0001c0013a0005c0006 | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.990A>G | p.Thr330Thr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/12 | 1101/5240 | 990/3171 | 330/1056 | chr17 | 45468527 | ||
chr17:45475171
|
G | A | 3 | a0001c0002a0001c0013a0005c0006 | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.852C>T | p.Cys284Cys | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 963/5240 | 852/3171 | 284/1056 | chr17 | 45475171 | ||
chr17:45475351
|
G | C | 3 | a0001c0002a0001c0013a0005c0006 | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.672C>G | p.Ser224Ser | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 783/5240 | 672/3171 | 224/1056 | chr17 | 45475351 | ||
chr17:45475446
|
A | G | 3 | a0001c0002a0001c0013a0005c0006 | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.577T>C | p.Leu193Leu | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 688/5240 | 577/3171 | 193/1056 | chr17 | 45475446 | ||
chr17:45475555
|
C | T | 3 | a0001c0002a0001c0013a0005c0006 | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
synonymous_variant | LOW | c.468G>A | p.Arg156Arg | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 579/5240 | 468/3171 | 156/1056 | chr17 | 45475555 | ||
chr17:45475576
|
G | A | 1 | a0001c0013 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.447C>T | p.Tyr149Tyr | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/12 | 558/5240 | 447/3171 | 149/1056 | chr17 | 45475576 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45435913
|
C | G | 1 | a0001c0009t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1945G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1945 | chr17 | 45435913 | |||||
chr17:45436075
|
C | T | 3 | a0001c0001t0005a0001c0002t0002a0005c0006t0002 | 23 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1783G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1783 | chr17 | 45436075 | |||||
chr17:45436152
|
C | T | 1 | a0001c0001t0005 | 3 | HG02886.hp2 HG03041.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1706G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1706 | chr17 | 45436152 | |||||
chr17:45436185
|
C | G | 2 | a0001c0002t0002a0005c0006t0002 | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1673G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1673 | chr17 | 45436185 | |||||
chr17:45436530
|
C | T | 2 | a0001c0002t0002a0005c0006t0002 | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1328 | chr17 | 45436530 | |||||
chr17:45436810
|
C | T | 1 | a0001c0001t0008 | 2 | HG01891.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1048G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 1048 | chr17 | 45436810 | |||||
chr17:45437026
|
C | T | 2 | a0001c0001t0013a0001c0009t0012 | 2 | HG02647.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*832G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 832 | chr17 | 45437026 | |||||
chr17:45437045
|
G | C | 3 | a0001c0001t0003a0001c0010t0003a0001c0011t0003 | 17 | HG00280.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*813C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 813 | chr17 | 45437045 | |||||
chr17:45437171
|
G | C | 1 | a0001c0001t0004 | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*687C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 687 | chr17 | 45437171 | |||||
chr17:45437223
|
G | C | 1 | a0001c0001t0006 | 3 | HG00642.hp2 HG01081.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*635C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 635 | chr17 | 45437223 | |||||
chr17:45437336
|
G | A | 1 | a0001c0001t0014 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*522C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 522 | chr17 | 45437336 | |||||
chr17:45437366
|
T | C | 1 | a0001c0001t0015 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 492 | chr17 | 45437366 | |||||
chr17:45437496
|
G | T | 1 | a0001c0001t0011 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 362 | chr17 | 45437496 | |||||
chr17:45437555
|
C | T | 1 | a0001c0001t0010 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 303 | chr17 | 45437555 | |||||
chr17:45437588
|
G | A | 2 | a0001c0002t0002a0005c0006t0002 | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 270 | chr17 | 45437588 | |||||
chr17:45437839
|
C | T | 1 | a0001c0001t0007 | 2 | HG03669.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*19G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 12/12 | 19 | chr17 | 45437839 | |||||
chr17:45490678
|
G | C | 1 | a0001c0001t0016 | 1 | HG00099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/12 | 8194 | chr17 | 45490678 | |||||
chr17:45490707
|
C | T | 2 | a0001c0001t0004a0001c0001t0009 | 6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/12 | 8223 | chr17 | 45490707 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:45437993
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0130 | 4 | HG00099.hp2 HG00597.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.3060-24G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45437993 | ||||||
chr17:45438116
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3060-147C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438116 | ||||||
chr17:45438300
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3060-331C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438300 | ||||||
chr17:45438398
|
G | A | 1 | a0001c0002t0002g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3060-429C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438398 | ||||||
chr17:45438457
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3060-488C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438457 | ||||||
chr17:45438480
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3060-511G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438480 | ||||||
chr17:45438519
|
A | G | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3060-550T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438519 | ||||||
chr17:45438547
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3060-578T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438547 | ||||||
chr17:45438561
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3060-592G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438561 | ||||||
chr17:45438619
|
C | A | 2 | a0001c0001t0003g0136a0001c0001t0003g0145 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.3060-650G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438619 | ||||||
chr17:45438760
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3059+717A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438760 | ||||||
chr17:45438809
|
G | A | 2 | a0001c0002t0002g0009a0001c0002t0002g0063 | 4 | HG01074.hp2 HG01123.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3059+668C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438809 | ||||||
chr17:45438812
|
C | T | 4 | a0001c0004t0001g0048a0001c0004t0001g0049a0001c0004t0001g0050others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3059+665G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438812 | ||||||
chr17:45438839
|
G | C | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3059+638C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438839 | ||||||
chr17:45438854
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3059+623C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438854 | ||||||
chr17:45438909
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3059+568G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438909 | ||||||
chr17:45438923
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3059+554G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45438923 | ||||||
chr17:45439036
|
A | G | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3059+441T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439036 | ||||||
chr17:45439108
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3059+369G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439108 | ||||||
chr17:45439178
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3059+299G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439178 | ||||||
chr17:45439231
|
T | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0243 | 2 | NA18967.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.3059+246A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439231 | ||||||
chr17:45439372
|
A | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(174): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3059+105T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439372 | ||||||
chr17:45439373
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.3059+104C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 11/11 | chr17 | 45439373 | ||||||
chr17:45439688
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2902-54C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 10/11 | chr17 | 45439688 | ||||||
chr17:45439768
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2902-134G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 10/11 | chr17 | 45439768 | ||||||
chr17:45439886
|
T | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2902-252A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 10/11 | chr17 | 45439886 | ||||||
chr17:45440366
|
C | T | 1 | a0001c0001t0003g0026 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2838-140G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440366 | ||||||
chr17:45440490
|
A | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0055 | 3 | HG02280.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2838-264T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440490 | ||||||
chr17:45440608
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2838-382C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440608 | ||||||
chr17:45440786
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(169): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2838-560T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440786 | ||||||
chr17:45440962
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2838-736G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45440962 | ||||||
chr17:45441034
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2838-808C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441034 | ||||||
chr17:45441538
|
G | A | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2838-1312C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441538 | ||||||
chr17:45441780
|
G | A | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2838-1554C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441780 | ||||||
chr17:45441870
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2838-1644A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45441870 | ||||||
chr17:45442086
|
A | G | 16 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0091others(13): Show | 17 | HG00735.hp1 HG01884.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2838-1860T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442086 | ||||||
chr17:45442185
|
G | A | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2838-1959C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442185 | ||||||
chr17:45442198
|
C | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2838-1972G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442198 | ||||||
chr17:45442261
|
A | G | 1 | a0001c0001t0003g0026 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2838-2035T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442261 | ||||||
chr17:45442370
|
A | T | 3 | a0001c0005t0001g0075a0001c0005t0001g0246a0001c0005t0001g0247 | 3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2838-2144T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442370 | ||||||
chr17:45442394
|
G | T | 2 | a0001c0001t0003g0136a0001c0001t0003g0145 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2838-2168C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442394 | ||||||
chr17:45442593
|
C | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2838-2367G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442593 | ||||||
chr17:45442723
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2838-2497G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442723 | ||||||
chr17:45442752
|
A | G | 26 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(23): Show | 31 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.2838-2526T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442752 | ||||||
chr17:45442906
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+2564C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45442906 | ||||||
chr17:45443032
|
G | T | 14 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0032others(11): Show | 17 | HG00280.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.2837+2438C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443032 | ||||||
chr17:45443092
|
C | G | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2837+2378G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443092 | ||||||
chr17:45443147
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2837+2323A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443147 | ||||||
chr17:45443188
|
A | G | 1 | a0001c0001t0003g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2837+2282T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443188 | ||||||
chr17:45443309
|
T | C | 26 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(23): Show | 31 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.2837+2161A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443309 | ||||||
chr17:45443494
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18966.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2837+1976C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443494 | ||||||
chr17:45443623
|
G | A | 1 | a0001c0005t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2837+1847C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443623 | ||||||
chr17:45443628
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0103others(6): Show | 12 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2837+1842C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443628 | ||||||
chr17:45443795
|
C | G | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+1675G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443795 | ||||||
chr17:45443827
|
A | G | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+1643T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45443827 | ||||||
chr17:45444028
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2837+1442C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444028 | ||||||
chr17:45444069
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2837+1401C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444069 | ||||||
chr17:45444096
|
C | T | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2837+1374G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444096 | ||||||
chr17:45444097
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2837+1373C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444097 | ||||||
chr17:45444185
|
G | A | 1 | a0001c0001t0006g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2837+1285C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444185 | ||||||
chr17:45444219
|
G | T | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2837+1251C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444219 | ||||||
chr17:45444304
|
C | T | 1 | a0001c0005t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2837+1166G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444304 | ||||||
chr17:45444557
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2837+913C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444557 | ||||||
chr17:45444876
|
AGATGGAG others(42): Show |
A | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2837+545_2837+593d others(51): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444876 | ||||||
chr17:45444974
|
G | A | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0235 | 3 | NA18747.hp1 NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2837+496C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444974 | ||||||
chr17:45444995
|
T | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+475A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45444995 | ||||||
chr17:45445027
|
G | A | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2837+443C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445027 | ||||||
chr17:45445080
|
C | G | 2 | a0001c0001t0001g0058a0001c0002t0001g0074 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2837+390G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445080 | ||||||
chr17:45445112
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2837+358T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445112 | ||||||
chr17:45445201
|
C | G | 3 | a0001c0005t0001g0075a0001c0005t0001g0246a0001c0005t0001g0247 | 3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2837+269G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445201 | ||||||
chr17:45445240
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2837+230C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445240 | ||||||
chr17:45445245
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2837+225C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445245 | ||||||
chr17:45445409
|
TTGTG | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2837+57_2837+60del others(4): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445409 | ||||||
chr17:45445434
|
C | T | 2 | a0001c0001t0001g0058a0001c0002t0001g0074 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2837+36G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445434 | ||||||
chr17:45445446
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2837+24G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 9/11 | chr17 | 45445446 | ||||||
chr17:45446019
|
T | TC | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-357dupG | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446019 | ||||||
chr17:45446080
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2644-417C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446080 | ||||||
chr17:45446241
|
A | G | 1 | a0001c0005t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2644-578T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446241 | ||||||
chr17:45446372
|
C | T | 1 | a0001c0002t0002g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2644-709G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446372 | ||||||
chr17:45446396
|
G | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0137others(1): Show | 4 | HG01106.hp2 HG01175.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.2644-733C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446396 | ||||||
chr17:45446520
|
G | A | 2 | a0001c0005t0001g0075a0001c0005t0001g0247 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2644-857C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446520 | ||||||
chr17:45446654
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0011g0191 | 2 | HG01358.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2644-991G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446654 | ||||||
chr17:45446772
|
T | C | 2 | a0001c0002t0002g0060a0001c0002t0002g0066 | 2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2644-1109A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446772 | ||||||
chr17:45446979
|
C | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0105others(6): Show | 10 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2644-1316G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45446979 | ||||||
chr17:45447079
|
G | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0155 | 3 | HG02683.hp2 NA18951.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2644-1416C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447079 | ||||||
chr17:45447160
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-1497G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447160 | ||||||
chr17:45447361
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2644-1698C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447361 | ||||||
chr17:45447382
|
G | C | 1 | a0001c0005t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2644-1719C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447382 | ||||||
chr17:45447589
|
C | CCAGCCAG others(18): Show |
1 | a0001c0001t0008g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2644-1951_2644-192 others(29): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447589 | ||||||
chr17:45447589
|
CCAGCCAG others(18): Show |
C | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2644-1951_2644-192 others(29): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447589 | ||||||
chr17:45447656
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-1993C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447656 | ||||||
chr17:45447710
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2644-2047G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447710 | ||||||
chr17:45447800
|
C | CT | 19 | a0001c0001t0001g0225a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.2644-2138dupA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447800 | ||||||
chr17:45447800
|
CT | C | 5 | a0001c0001t0001g0112a0001c0001t0004g0018a0001c0001t0004g0040others(2): Show | 6 | HG02818.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2644-2138delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447800 | ||||||
chr17:45447839
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2644-2176G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447839 | ||||||
chr17:45447883
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2644-2220G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447883 | ||||||
chr17:45447922
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2644-2259C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447922 | ||||||
chr17:45447945
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2644-2282G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447945 | ||||||
chr17:45447980
|
TAG | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-2319_2644-231 others(6): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447980 | ||||||
chr17:45447999
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2644-2336G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45447999 | ||||||
chr17:45448331
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0222 | 5 | HG02074.hp1 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.2643+2287C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45448331 | ||||||
chr17:45448353
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2643+2265G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45448353 | ||||||
chr17:45448888
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2643+1730G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45448888 | ||||||
chr17:45449225
|
C | CAGCTCG | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2643+1392_2643+139 others(10): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449225 | ||||||
chr17:45449286
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2643+1332G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449286 | ||||||
chr17:45449289
|
TCCACCCA others(69): Show |
T | 1 | a0001c0001t0001g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2643+1253_2643+132 others(80): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449289 | ||||||
chr17:45449485
|
G | A | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2643+1133C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449485 | ||||||
chr17:45449581
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0047others(18): Show | 25 | HG00642.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2643+1037G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449581 | ||||||
chr17:45449659
|
C | T | 18 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(15): Show | 21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.2643+959G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449659 | ||||||
chr17:45449753
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2643+865G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449753 | ||||||
chr17:45449781
|
C | T | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2643+837G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449781 | ||||||
chr17:45449821
|
C | A | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2643+797G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449821 | ||||||
chr17:45449947
|
C | A | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2643+671G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449947 | ||||||
chr17:45449957
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2643+661G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45449957 | ||||||
chr17:45450170
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2643+448G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45450170 | ||||||
chr17:45450234
|
C | T | 1 | a0001c0001t0008g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2643+384G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45450234 | ||||||
chr17:45450311
|
T | TTATC | 2 | a0002c0003t0001g0008a0002c0003t0001g0054 | 4 | HG02896.hp2 HG02897.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2643+303_2643+306d others(6): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 8/11 | chr17 | 45450311 | ||||||
chr17:45450818
|
T | C | 1 | a0001c0001t0004g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2498-55A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45450818 | ||||||
chr17:45451215
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0101others(7): Show | 11 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2498-452C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451215 | ||||||
chr17:45451526
|
C | T | 8 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2498-763G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451526 | ||||||
chr17:45451583
|
A | G | 1 | a0001c0001t0011g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2498-820T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451583 | ||||||
chr17:45451790
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2498-1027C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451790 | ||||||
chr17:45451899
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2498-1136G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451899 | ||||||
chr17:45451927
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2498-1164C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451927 | ||||||
chr17:45451957
|
A | G | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2498-1194T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451957 | ||||||
chr17:45451975
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG01192.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2498-1212C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45451975 | ||||||
chr17:45452042
|
G | A | 1 | a0001c0005t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2498-1279C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452042 | ||||||
chr17:45452055
|
C | T | 1 | a0001c0001t0008g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2498-1292G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452055 | ||||||
chr17:45452290
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2497+1065T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452290 | ||||||
chr17:45452306
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2497+1049T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452306 | ||||||
chr17:45452321
|
T | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2497+1034A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452321 | ||||||
chr17:45452327
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2497+1028A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452327 | ||||||
chr17:45452349
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0008g0085a0001c0001t0008g0086 | 3 | HG01891.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2497+1006A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452349 | ||||||
chr17:45452362
|
A | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.2497+993T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452362 | ||||||
chr17:45452403
|
G | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2497+952C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452403 | ||||||
chr17:45452439
|
A | T | 1 | a0001c0001t0001g0162 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2497+916T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452439 | ||||||
chr17:45452567
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2497+788C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452567 | ||||||
chr17:45452728
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2497+627C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452728 | ||||||
chr17:45452791
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2497+564A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452791 | ||||||
chr17:45452792
|
G | T | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2497+563C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452792 | ||||||
chr17:45452937
|
A | G | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2497+418T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45452937 | ||||||
chr17:45453184
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.2497+171C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 7/11 | chr17 | 45453184 | ||||||
chr17:45454402
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0245a0001c0013t0001g0078 | 5 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-130G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454402 | ||||||
chr17:45454458
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1580-186C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454458 | ||||||
chr17:45454526
|
C | T | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1580-254G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454526 | ||||||
chr17:45454560
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1580-288G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454560 | ||||||
chr17:45454594
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1580-322C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454594 | ||||||
chr17:45454691
|
C | G | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1580-419G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454691 | ||||||
chr17:45454693
|
C | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1580-421G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454693 | ||||||
chr17:45454724
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1580-452G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454724 | ||||||
chr17:45454886
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1580-614G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454886 | ||||||
chr17:45454908
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1580-636G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454908 | ||||||
chr17:45454947
|
G | A | 1 | a0001c0005t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1580-675C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45454947 | ||||||
chr17:45455049
|
C | T | 2 | a0001c0001t0001g0058a0001c0002t0001g0074 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1580-777G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455049 | ||||||
chr17:45455050
|
G | A | 1 | a0001c0001t0001g0039 | 2 | HG00609.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1580-778C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455050 | ||||||
chr17:45455173
|
T | G | 2 | a0001c0001t0008g0085a0001c0001t0008g0086 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1580-901A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455173 | ||||||
chr17:45455212
|
C | T | 3 | a0002c0003t0001g0008a0002c0003t0001g0044a0002c0003t0001g0054 | 5 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-940G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455212 | ||||||
chr17:45455313
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1580-1041G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455313 | ||||||
chr17:45455320
|
C | T | 1 | a0001c0001t0008g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1580-1048G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455320 | ||||||
chr17:45455409
|
G | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1580-1137C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455409 | ||||||
chr17:45455438
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1580-1166G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455438 | ||||||
chr17:45455593
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1580-1321G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455593 | ||||||
chr17:45455702
|
C | T | 1 | a0001c0001t0001g0035 | 2 | NA18985.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1580-1430G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455702 | ||||||
chr17:45455921
|
G | T | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1580-1649C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455921 | ||||||
chr17:45455956
|
C | T | 1 | a0002c0003t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1580-1684G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45455956 | ||||||
chr17:45456166
|
A | G | 2 | a0001c0001t0008g0085a0001c0001t0008g0086 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1580-1894T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456166 | ||||||
chr17:45456201
|
T | C | 2 | a0001c0001t0001g0058a0001c0002t0001g0074 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1580-1929A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456201 | ||||||
chr17:45456595
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1579+1574C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456595 | ||||||
chr17:45456733
|
A | G | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1579+1436T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456733 | ||||||
chr17:45456956
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1579+1213A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456956 | ||||||
chr17:45456987
|
T | C | 34 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0091others(31): Show | 38 | HG00140.hp1 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1579+1182A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45456987 | ||||||
chr17:45457172
|
G | GA | 26 | a0001c0001t0001g0083a0001c0001t0001g0111a0001c0001t0001g0115others(23): Show | 29 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1579+996dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457172 | ||||||
chr17:45457172
|
GA | G | 7 | a0001c0001t0001g0109a0001c0001t0001g0183a0001c0001t0001g0195others(4): Show | 7 | HG01168.hp2 HG01993.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579+996delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457172 | ||||||
chr17:45457195
|
A | C | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1579+974T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457195 | ||||||
chr17:45457328
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1579+841G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457328 | ||||||
chr17:45457366
|
C | T | 1 | a0004c0012t0001g0182 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1579+803G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457366 | ||||||
chr17:45457560
|
CA | C | 6 | a0001c0001t0001g0161a0001c0001t0001g0214a0001c0001t0008g0085others(3): Show | 6 | HG01891.hp1 HG02922.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+608delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457560 | ||||||
chr17:45457681
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 10 | HG01168.hp2 HG01169.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1579+488A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45457681 | ||||||
chr17:45458067
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1579+102G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 6/11 | chr17 | 45458067 | ||||||
chr17:45458586
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(169): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1309-147G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45458586 | ||||||
chr17:45458618
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1309-179G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45458618 | ||||||
chr17:45458881
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1309-442G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45458881 | ||||||
chr17:45459024
|
A | C | 2 | a0001c0005t0001g0075a0001c0005t0001g0247 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1309-585T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459024 | ||||||
chr17:45459042
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-603G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459042 | ||||||
chr17:45459076
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0174 | 2 | HG01433.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1309-637G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459076 | ||||||
chr17:45459282
|
C | A | 1 | a0001c0004t0001g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1309-843G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459282 | ||||||
chr17:45459372
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1309-933G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459372 | ||||||
chr17:45459377
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-938G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459377 | ||||||
chr17:45459407
|
A | C | 1 | a0001c0002t0002g0065 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1309-968T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459407 | ||||||
chr17:45459604
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-1165C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459604 | ||||||
chr17:45459716
|
C | T | 2 | a0001c0001t0008g0085a0001c0001t0008g0086 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1309-1277G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459716 | ||||||
chr17:45459802
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(133): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1309-1363C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459802 | ||||||
chr17:45459915
|
T | G | 15 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0091others(12): Show | 16 | HG00735.hp1 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1309-1476A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45459915 | ||||||
chr17:45460103
|
T | C | 1 | a0001c0001t0003g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1309-1664A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460103 | ||||||
chr17:45460195
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1309-1756C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460195 | ||||||
chr17:45460345
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-1906G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460345 | ||||||
chr17:45460384
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1309-1945G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460384 | ||||||
chr17:45460395
|
G | A | 2 | a0001c0001t0008g0085a0001c0001t0008g0086 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1309-1956C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460395 | ||||||
chr17:45460420
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1309-1981G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460420 | ||||||
chr17:45460652
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1309-2213C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460652 | ||||||
chr17:45460731
|
A | G | 3 | a0001c0001t0001g0185a0001c0001t0001g0192a0001c0001t0011g0191 | 3 | HG01358.hp1 HG03654.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1309-2292T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460731 | ||||||
chr17:45460947
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1309-2508G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45460947 | ||||||
chr17:45461157
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-2718C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461157 | ||||||
chr17:45461163
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1309-2724T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461163 | ||||||
chr17:45461340
|
T | C | 2 | a0001c0001t0001g0141a0003c0007t0001g0079 | 2 | HG00735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1309-2901A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461340 | ||||||
chr17:45461441
|
T | G | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3002A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461441 | ||||||
chr17:45461625
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3186C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461625 | ||||||
chr17:45461627
|
G | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3188C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461627 | ||||||
chr17:45461669
|
G | A | 19 | a0001c0001t0001g0231a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1309-3230C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461669 | ||||||
chr17:45461705
|
T | C | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1309-3266A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461705 | ||||||
chr17:45461716
|
C | T | 2 | a0001c0001t0001g0058a0001c0002t0001g0074 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1309-3277G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461716 | ||||||
chr17:45461737
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1309-3298T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461737 | ||||||
chr17:45461839
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0228 | 2 | NA18960.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1309-3400A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45461839 | ||||||
chr17:45462010
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1309-3571A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462010 | ||||||
chr17:45462045
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1309-3606G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462045 | ||||||
chr17:45462071
|
C | G | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3632G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462071 | ||||||
chr17:45462095
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | NA18964.hp2 NA18966.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309-3656C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462095 | ||||||
chr17:45462250
|
C | T | 2 | a0001c0001t0001g0058a0001c0002t0001g0074 | 2 | HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1309-3811G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462250 | ||||||
chr17:45462357
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-3918G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462357 | ||||||
chr17:45462505
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1309-4066G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462505 | ||||||
chr17:45462585
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1309-4146C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462585 | ||||||
chr17:45462598
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1309-4159A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462598 | ||||||
chr17:45462602
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4163C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462602 | ||||||
chr17:45462678
|
G | A | 1 | a0001c0001t0008g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1309-4239C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462678 | ||||||
chr17:45462907
|
C | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4468G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45462907 | ||||||
chr17:45463071
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(190): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1309-4632T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463071 | ||||||
chr17:45463083
|
G | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4644C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463083 | ||||||
chr17:45463085
|
C | CA | 8 | a0001c0001t0001g0144a0001c0001t0001g0195a0001c0001t0001g0205others(5): Show | 8 | HG01168.hp1 HG01168.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-4647dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463085 | ||||||
chr17:45463085
|
CA | C | 19 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0091others(16): Show | 22 | HG00609.hp2 HG01884.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1309-4647delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463085 | ||||||
chr17:45463106
|
A | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1309-4667T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463106 | ||||||
chr17:45463192
|
C | T | 1 | a0001c0001t0001g0038 | 2 | NA18973.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1309-4753G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463192 | ||||||
chr17:45463223
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1309-4784A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463223 | ||||||
chr17:45463314
|
C | T | 1 | a0001c0004t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1309-4875G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463314 | ||||||
chr17:45463345
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0116 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1308+4864C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463345 | ||||||
chr17:45463366
|
T | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+4843A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463366 | ||||||
chr17:45463515
|
C | T | 1 | a0001c0001t0006g0142 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1308+4694G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463515 | ||||||
chr17:45463519
|
A | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0228 | 2 | NA18960.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1308+4690T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463519 | ||||||
chr17:45463705
|
T | C | 2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1308+4504A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463705 | ||||||
chr17:45463718
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1308+4491G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463718 | ||||||
chr17:45463763
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(173): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1308+4446G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463763 | ||||||
chr17:45463793
|
C | T | 1 | a0001c0001t0001g0029 | 2 | HG00673.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1308+4416G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463793 | ||||||
chr17:45463850
|
G | A | 1 | a0001c0004t0001g0052 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1308+4359C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463850 | ||||||
chr17:45463853
|
A | G | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1308+4356T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463853 | ||||||
chr17:45463854
|
C | T | 2 | a0001c0001t0001g0231a0001c0009t0012g0057 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1308+4355G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463854 | ||||||
chr17:45463954
|
A | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0129a0001c0001t0001g0130 | 5 | HG00099.hp2 HG00597.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+4255T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45463954 | ||||||
chr17:45464219
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1308+3990C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464219 | ||||||
chr17:45464261
|
C | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+3948G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464261 | ||||||
chr17:45464290
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+3919G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464290 | ||||||
chr17:45464448
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1308+3761C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464448 | ||||||
chr17:45464468
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1308+3741G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464468 | ||||||
chr17:45464514
|
C | T | 3 | a0001c0005t0001g0075a0001c0005t0001g0246a0001c0005t0001g0247 | 3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+3695G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464514 | ||||||
chr17:45464552
|
G | C | 3 | a0001c0005t0001g0075a0001c0005t0001g0246a0001c0005t0001g0247 | 3 | HG02922.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+3657C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464552 | ||||||
chr17:45464671
|
T | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+3538A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464671 | ||||||
chr17:45464761
|
T | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1308+3448A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464761 | ||||||
chr17:45464859
|
G | A | 8 | a0001c0004t0001g0048a0001c0004t0001g0049a0001c0004t0001g0050others(5): Show | 10 | HG02257.hp2 HG02647.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1308+3350C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464859 | ||||||
chr17:45464871
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1308+3338G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464871 | ||||||
chr17:45464910
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1308+3299G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464910 | ||||||
chr17:45464935
|
C | T | 18 | a0001c0001t0001g0231a0001c0002t0002g0009a0001c0002t0002g0020others(15): Show | 21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1308+3274G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464935 | ||||||
chr17:45464940
|
T | C | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1308+3269A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464940 | ||||||
chr17:45464993
|
G | A | 1 | a0001c0004t0001g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1308+3216C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45464993 | ||||||
chr17:45465042
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1308+3167G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465042 | ||||||
chr17:45465046
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1308+3163A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465046 | ||||||
chr17:45465282
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1308+2927A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465282 | ||||||
chr17:45465430
|
C | T | 8 | a0001c0001t0001g0053a0001c0004t0001g0048a0001c0004t0001g0049others(5): Show | 10 | HG02257.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1308+2779G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465430 | ||||||
chr17:45465625
|
A | G | 1 | a0001c0001t0003g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1308+2584T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465625 | ||||||
chr17:45465698
|
A | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(58): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1308+2511T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465698 | ||||||
chr17:45465709
|
C | CA | 16 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0090others(13): Show | 19 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1308+2499dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465709 | ||||||
chr17:45465716
|
A | AT | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(113): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1308+2492dupA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465716 | ||||||
chr17:45465717
|
T | A | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1308+2492A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465717 | ||||||
chr17:45465841
|
T | C | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1308+2368A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45465841 | ||||||
chr17:45466122
|
C | A | 1 | a0001c0001t0009g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1308+2087G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466122 | ||||||
chr17:45466132
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1308+2077C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466132 | ||||||
chr17:45466206
|
A | G | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+2003T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466206 | ||||||
chr17:45466299
|
T | C | 2 | a0001c0009t0012g0057a0001c0013t0001g0078 | 2 | HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1308+1910A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466299 | ||||||
chr17:45466306
|
T | A | 1 | a0001c0001t0001g0156 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1308+1903A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466306 | ||||||
chr17:45466464
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(171): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1308+1745A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466464 | ||||||
chr17:45466840
|
G | C | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1308+1369C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466840 | ||||||
chr17:45466888
|
A | G | 1 | a0001c0005t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1308+1321T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45466888 | ||||||
chr17:45467004
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18966.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1308+1205A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467004 | ||||||
chr17:45467013
|
G | A | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1308+1196C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467013 | ||||||
chr17:45467090
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1308+1119C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467090 | ||||||
chr17:45467459
|
C | T | 1 | a0001c0001t0015g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1308+750G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467459 | ||||||
chr17:45467587
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1308+622G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467587 | ||||||
chr17:45467734
|
C | T | 1 | a0001c0001t0008g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1308+475G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467734 | ||||||
chr17:45467770
|
C | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0076others(10): Show | 16 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1308+439G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467770 | ||||||
chr17:45467934
|
C | T | 13 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.1308+275G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 5/11 | chr17 | 45467934 | ||||||
chr17:45468631
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.924-38C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468631 | ||||||
chr17:45468691
|
G | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.924-98C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468691 | ||||||
chr17:45468817
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.924-224C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468817 | ||||||
chr17:45468858
|
G | A | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.924-265C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468858 | ||||||
chr17:45468931
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.924-338G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468931 | ||||||
chr17:45468956
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.924-363C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45468956 | ||||||
chr17:45469024
|
C | CTG | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-433_924-432dup others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469024 | ||||||
chr17:45469076
|
A | G | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-483T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469076 | ||||||
chr17:45469297
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.924-704G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469297 | ||||||
chr17:45469474
|
T | G | 1 | a0001c0001t0008g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.924-881A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469474 | ||||||
chr17:45469487
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.924-894C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469487 | ||||||
chr17:45469612
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.924-1019G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469612 | ||||||
chr17:45469839
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.924-1246A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469839 | ||||||
chr17:45469871
|
A | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0090others(12): Show | 18 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.924-1278T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469871 | ||||||
chr17:45469911
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.924-1318T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469911 | ||||||
chr17:45469966
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.924-1373T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45469966 | ||||||
chr17:45470115
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.924-1522T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470115 | ||||||
chr17:45470193
|
G | A | 4 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(1): Show | 4 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1600C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470193 | ||||||
chr17:45470343
|
C | T | 15 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0090others(12): Show | 18 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.924-1750G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470343 | ||||||
chr17:45470424
|
T | C | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-1831A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470424 | ||||||
chr17:45470448
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.924-1855C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470448 | ||||||
chr17:45470544
|
AC | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0092others(9): Show | 13 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.924-1952delG | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470544 | ||||||
chr17:45470558
|
C | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.924-1965G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470558 | ||||||
chr17:45470558
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.924-1965G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470558 | ||||||
chr17:45470658
|
G | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0097a0001c0005t0001g0246 | 4 | HG01167.hp1 HG01169.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-2065C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470658 | ||||||
chr17:45470682
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.924-2089A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470682 | ||||||
chr17:45470690
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.924-2097T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470690 | ||||||
chr17:45470781
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.924-2188G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470781 | ||||||
chr17:45470955
|
T | C | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-2362A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45470955 | ||||||
chr17:45471022
|
TG | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.924-2430delC | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471022 | ||||||
chr17:45471058
|
A | G | 18 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(15): Show | 21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.924-2465T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471058 | ||||||
chr17:45471073
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.924-2480A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471073 | ||||||
chr17:45471115
|
A | G | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.924-2522T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471115 | ||||||
chr17:45471305
|
A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(175): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.924-2712T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471305 | ||||||
chr17:45471343
|
GGT | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.924-2752_924-2751d others(4): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471343 | ||||||
chr17:45471346
|
G | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.924-2753C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471346 | ||||||
chr17:45471367
|
C | G | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.924-2774G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471367 | ||||||
chr17:45471412
|
G | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(108): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.924-2819C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471412 | ||||||
chr17:45471537
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 4 | HG00609.hp1 NA18973.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2944G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471537 | ||||||
chr17:45471584
|
T | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0076others(3): Show | 8 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.924-2991A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471584 | ||||||
chr17:45471762
|
T | C | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.924-3169A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471762 | ||||||
chr17:45471833
|
G | A | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.924-3240C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471833 | ||||||
chr17:45471925
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.923+3175G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471925 | ||||||
chr17:45471992
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.923+3108G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471992 | ||||||
chr17:45471993
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.923+3107C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45471993 | ||||||
chr17:45472000
|
A | G | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.923+3100T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472000 | ||||||
chr17:45472009
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.923+3091A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472009 | ||||||
chr17:45472031
|
T | C | 1 | a0001c0002t0002g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.923+3069A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472031 | ||||||
chr17:45472097
|
G | A | 1 | a0001c0010t0003g0240 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.923+3003C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472097 | ||||||
chr17:45472133
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.923+2967A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472133 | ||||||
chr17:45472137
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.923+2963C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472137 | ||||||
chr17:45472160
|
A | G | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+2940T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472160 | ||||||
chr17:45472164
|
C | CGGTGAGA others(37): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0087others(2): Show | 7 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+2892_923+2935d others(46): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472164 | ||||||
chr17:45472207
|
C | G | 1 | a0001c0005t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.923+2893G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472207 | ||||||
chr17:45472242
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+2858C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472242 | ||||||
chr17:45472331
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0229 | 2 | NA18980.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.923+2769A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472331 | ||||||
chr17:45472430
|
C | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0076others(10): Show | 16 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.923+2670G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472430 | ||||||
chr17:45472467
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0183 | 2 | HG00609.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.923+2633C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472467 | ||||||
chr17:45472741
|
A | G | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+2359T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472741 | ||||||
chr17:45472744
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.923+2356T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472744 | ||||||
chr17:45472920
|
C | T | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.923+2180G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472920 | ||||||
chr17:45472984
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.923+2116A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45472984 | ||||||
chr17:45473145
|
G | C | 1 | a0001c0005t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1955C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473145 | ||||||
chr17:45473155
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.923+1945C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473155 | ||||||
chr17:45473220
|
C | T | 3 | a0001c0001t0006g0120a0001c0001t0006g0127a0001c0001t0006g0142 | 3 | HG00642.hp2 HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.923+1880G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473220 | ||||||
chr17:45473221
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.923+1879G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473221 | ||||||
chr17:45473346
|
T | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.923+1754A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473346 | ||||||
chr17:45473415
|
C | A | 1 | a0001c0011t0003g0150 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.923+1685G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473415 | ||||||
chr17:45473563
|
AT | A | 20 | a0001c0001t0001g0023a0001c0002t0001g0074a0001c0002t0002g0009others(17): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.923+1536delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473563 | ||||||
chr17:45473575
|
T | C | 1 | a0001c0001t0001g0017 | 3 | NA18988.hp1 NA18989.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.923+1525A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473575 | ||||||
chr17:45473644
|
C | T | 10 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0101others(7): Show | 11 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+1456G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473644 | ||||||
chr17:45473653
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.923+1447C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473653 | ||||||
chr17:45473717
|
C | T | 18 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(15): Show | 21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.923+1383G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473717 | ||||||
chr17:45473720
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(5): Show | 10 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.923+1380C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473720 | ||||||
chr17:45473731
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.923+1369A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473731 | ||||||
chr17:45473780
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.923+1320C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473780 | ||||||
chr17:45473785
|
C | G | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+1315G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473785 | ||||||
chr17:45473809
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.923+1291G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473809 | ||||||
chr17:45473838
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.923+1262C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473838 | ||||||
chr17:45473955
|
G | C | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+1145C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45473955 | ||||||
chr17:45474062
|
A | T | 15 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 18 | HG01243.hp1 HG01256.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.923+1038T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474062 | ||||||
chr17:45474062
|
AT | A | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+1037delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474062 | ||||||
chr17:45474066
|
T | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(25): Show | 45 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.923+1034A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474066 | ||||||
chr17:45474157
|
T | C | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+943A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474157 | ||||||
chr17:45474180
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.923+920G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474180 | ||||||
chr17:45474247
|
C | T | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.923+853G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474247 | ||||||
chr17:45474306
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.923+794G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474306 | ||||||
chr17:45474358
|
C | CA | 13 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 16 | HG01243.hp1 HG02257.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.923+741dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474358 | ||||||
chr17:45474582
|
C | T | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.923+518G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474582 | ||||||
chr17:45474740
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(135): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.923+360G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474740 | ||||||
chr17:45474823
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0200 | 5 | HG01891.hp2 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+277G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474823 | ||||||
chr17:45474888
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.923+212C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45474888 | ||||||
chr17:45475019
|
T | C | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.923+81A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45475019 | ||||||
chr17:45475086
|
G | A | 1 | a0001c0001t0006g0142 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.923+14C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 4/11 | chr17 | 45475086 | ||||||
chr17:45475784
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(122): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.297-58A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45475784 | ||||||
chr17:45476064
|
T | C | 1 | a0001c0001t0003g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.297-338A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476064 | ||||||
chr17:45476130
|
AAT | A | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.297-406_297-405del others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476130 | ||||||
chr17:45476145
|
A | T | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.297-419T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476145 | ||||||
chr17:45476162
|
A | C | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.297-436T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476162 | ||||||
chr17:45476198
|
TTA | T | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.297-474_297-473del others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476198 | ||||||
chr17:45476223
|
T | C | 1 | a0001c0001t0009g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.297-497A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476223 | ||||||
chr17:45476345
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.297-619C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476345 | ||||||
chr17:45476362
|
T | C | 1 | a0001c0001t0001g0037 | 2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.297-636A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476362 | ||||||
chr17:45476691
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297-965G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476691 | ||||||
chr17:45476787
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.297-1061G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476787 | ||||||
chr17:45476872
|
C | A | 2 | a0001c0002t0002g0064a0001c0002t0002g0068 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.296+1028G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45476872 | ||||||
chr17:45477035
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.296+865C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477035 | ||||||
chr17:45477337
|
G | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0093others(7): Show | 11 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.296+563C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477337 | ||||||
chr17:45477429
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(175): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.296+471T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477429 | ||||||
chr17:45477433
|
C | CAAA | 15 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(12): Show | 18 | HG00140.hp1 HG01074.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.296+464_296+466dup others(3): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477433 | ||||||
chr17:45477434
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.296+466T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477434 | ||||||
chr17:45477438
|
A | G | 5 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(2): Show | 6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.296+462T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477438 | ||||||
chr17:45477536
|
T | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(174): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.296+364A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477536 | ||||||
chr17:45477766
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.296+134G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477766 | ||||||
chr17:45477887
|
A | G | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.296+13T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 3/11 | chr17 | 45477887 | ||||||
chr17:45478236
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-89C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478236 | ||||||
chr17:45478395
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0201a0001c0001t0001g0202 | 4 | HG00738.hp1 HG01943.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-248A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478395 | ||||||
chr17:45478659
|
T | C | 2 | a0001c0002t0002g0069a0001c0002t0002g0070 | 2 | NA19085.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.49-512A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478659 | ||||||
chr17:45478777
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.49-630C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478777 | ||||||
chr17:45478826
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.49-679C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478826 | ||||||
chr17:45478898
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.49-751A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478898 | ||||||
chr17:45478901
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.49-754C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45478901 | ||||||
chr17:45479026
|
CT | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.49-880delA | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479026 | ||||||
chr17:45479208
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.49-1061A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479208 | ||||||
chr17:45479286
|
G | A | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.49-1139C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479286 | ||||||
chr17:45479315
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0212 | 2 | HG01069.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.49-1168G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479315 | ||||||
chr17:45479368
|
A | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(122): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.49-1221T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479368 | ||||||
chr17:45479441
|
T | C | 29 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(26): Show | 34 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.49-1294A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479441 | ||||||
chr17:45479496
|
C | T | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.49-1349G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479496 | ||||||
chr17:45479512
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(108): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.49-1365G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479512 | ||||||
chr17:45479517
|
C | CA | 23 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0098others(20): Show | 25 | HG00738.hp2 HG02027.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.49-1371dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479517 | ||||||
chr17:45479517
|
CA | C | 33 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0038others(30): Show | 42 | HG00140.hp1 HG00609.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.49-1371delT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479517 | ||||||
chr17:45479538
|
T | A | 1 | a0001c0001t0001g0220 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.49-1391A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479538 | ||||||
chr17:45479616
|
G | A | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-1469C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479616 | ||||||
chr17:45479688
|
A | AAAAAC | 4 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0234others(1): Show | 4 | HG01993.hp1 NA18747.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.49-1546_49-1542dup others(5): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479688 | ||||||
chr17:45479688
|
A | AAAAACAA others(3): Show |
19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-1551_49-1542dup others(10): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479688 | ||||||
chr17:45479688
|
AAAAAC | A | 5 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(2): Show | 6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-1546_49-1542del others(5): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479688 | ||||||
chr17:45479995
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49-1848A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479995 | ||||||
chr17:45479996
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49-1849T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45479996 | ||||||
chr17:45480246
|
G | A | 19 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(16): Show | 22 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.49-2099C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480246 | ||||||
chr17:45480321
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.48+2116G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480321 | ||||||
chr17:45480341
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0087others(2): Show | 7 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+2096C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480341 | ||||||
chr17:45480438
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.48+1999A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480438 | ||||||
chr17:45480439
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(153): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.48+1998C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480439 | ||||||
chr17:45480479
|
G | A | 1 | a0001c0001t0001g0037 | 2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.48+1958C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480479 | ||||||
chr17:45480482
|
TCAAAAAA others(1): Show |
T | 23 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0001g0106others(20): Show | 26 | HG00140.hp1 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.48+1947_48+1954del others(8): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480482 | ||||||
chr17:45480498
|
A | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+1939T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480498 | ||||||
chr17:45480511
|
A | C | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.48+1926T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480511 | ||||||
chr17:45480519
|
C | CA | 8 | a0001c0001t0001g0023a0001c0001t0001g0124a0001c0001t0001g0144others(5): Show | 9 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+1917dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480519 | ||||||
chr17:45480726
|
C | T | 18 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(15): Show | 21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.48+1711G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480726 | ||||||
chr17:45480766
|
T | C | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.48+1671A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480766 | ||||||
chr17:45480793
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.48+1644A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480793 | ||||||
chr17:45480850
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.48+1587G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480850 | ||||||
chr17:45480901
|
A | G | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+1536T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45480901 | ||||||
chr17:45481034
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.48+1403G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481034 | ||||||
chr17:45481369
|
G | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(7): Show | 12 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.48+1068C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481369 | ||||||
chr17:45481483
|
G | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0090others(12): Show | 18 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.48+954C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481483 | ||||||
chr17:45481647
|
C | T | 5 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(2): Show | 6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+790G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481647 | ||||||
chr17:45481662
|
G | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.48+775C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481662 | ||||||
chr17:45481834
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.48+603C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481834 | ||||||
chr17:45481860
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.48+577T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481860 | ||||||
chr17:45481904
|
T | G | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.48+533A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481904 | ||||||
chr17:45481917
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.48+520T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481917 | ||||||
chr17:45481929
|
G | C | 1 | a0001c0005t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.48+508C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481929 | ||||||
chr17:45481974
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.48+463A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45481974 | ||||||
chr17:45482133
|
C | A | 1 | a0001c0011t0003g0150 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.48+304G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482133 | ||||||
chr17:45482332
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | NA18964.hp2 NA18966.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+105T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482332 | ||||||
chr17:45482360
|
A | ATTCATT | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(167): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.48+76_48+77insAATG others(2): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482360 | ||||||
chr17:45482361
|
A | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(167): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.48+76T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482361 | ||||||
chr17:45482362
|
G | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(167): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.48+75C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482362 | ||||||
chr17:45482377
|
C | A | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.48+60G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482377 | ||||||
chr17:45482392
|
C | T | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.48+45G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 2/11 | chr17 | 45482392 | ||||||
chr17:45482589
|
C | T | 1 | a0001c0002t0002g0072 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-41-64G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482589 | ||||||
chr17:45482647
|
C | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-122G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482647 | ||||||
chr17:45482829
|
T | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-304A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482829 | ||||||
chr17:45482850
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-41-325C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482850 | ||||||
chr17:45482882
|
C | A | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-41-357G>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482882 | ||||||
chr17:45482885
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-360C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482885 | ||||||
chr17:45482919
|
A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(175): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-41-394T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482919 | ||||||
chr17:45482922
|
G | T | 1 | a0001c0013t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-41-397C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45482922 | ||||||
chr17:45483108
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(8): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-583G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483108 | ||||||
chr17:45483146
|
T | G | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-41-621A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483146 | ||||||
chr17:45483224
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-41-699C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483224 | ||||||
chr17:45483324
|
C | T | 3 | a0001c0005t0001g0246a0001c0005t0001g0247a0001c0013t0001g0078 | 3 | HG02559.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-41-799G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483324 | ||||||
chr17:45483335
|
T | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(9): Show | 16 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-41-810A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483335 | ||||||
chr17:45483414
|
T | TGGGTG | 3 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG01243.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-894_-41-890dup others(5): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483414 | ||||||
chr17:45483414
|
TGGGTGGG others(8): Show |
T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(10): Show | 17 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-41-904_-41-890del others(15): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483414 | ||||||
chr17:45483449
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(22): Show | 38 | HG00099.hp1 HG00323.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-41-924C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483449 | ||||||
chr17:45483550
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-41-1025G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483550 | ||||||
chr17:45483692
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-41-1167G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483692 | ||||||
chr17:45483761
|
T | C | 1 | a0001c0001t0009g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-41-1236A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45483761 | ||||||
chr17:45484364
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-41-1839G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484364 | ||||||
chr17:45484399
|
T | C | 1 | a0001c0001t0014g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-41-1874A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484399 | ||||||
chr17:45484499
|
C | T | 1 | a0001c0004t0001g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41-1974G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484499 | ||||||
chr17:45484678
|
C | T | 1 | a0001c0001t0006g0120 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41-2153G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484678 | ||||||
chr17:45484845
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-41-2320C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484845 | ||||||
chr17:45484866
|
C | T | 1 | a0002c0003t0001g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-41-2341G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484866 | ||||||
chr17:45484890
|
G | A | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG02559.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-41-2365C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45484890 | ||||||
chr17:45485092
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-2567A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485092 | ||||||
chr17:45485184
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0243 | 2 | NA18967.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-41-2659C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485184 | ||||||
chr17:45485194
|
G | GAAAAGGG others(6): Show |
2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-41-2682_-41-2670d others(15): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485194 | ||||||
chr17:45485512
|
T | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0092others(8): Show | 12 | HG00735.hp1 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41-2987A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485512 | ||||||
chr17:45485612
|
A | T | 1 | a0001c0001t0015g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-41-3087T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485612 | ||||||
chr17:45485727
|
A | G | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3202T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485727 | ||||||
chr17:45485736
|
T | TA | 7 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0004t0001g0048others(4): Show | 7 | HG02257.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-3212dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485736 | ||||||
chr17:45485775
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-3250A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485775 | ||||||
chr17:45485816
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 16 | HG00597.hp2 HG00609.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-41-3291C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485816 | ||||||
chr17:45485832
|
C | T | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-41-3307G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485832 | ||||||
chr17:45485938
|
A | C | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3413T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485938 | ||||||
chr17:45485939
|
T | G | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3414A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485939 | ||||||
chr17:45485983
|
G | A | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3458C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485983 | ||||||
chr17:45485992
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0121others(34): Show | 42 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-41-3467C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45485992 | ||||||
chr17:45486029
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-41-3504T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486029 | ||||||
chr17:45486060
|
C | CA | 5 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(2): Show | 6 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-3536dupT | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486060 | ||||||
chr17:45486078
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0189 | 4 | NA18942.hp2 NA18980.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-3553C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486078 | ||||||
chr17:45486114
|
G | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(6): Show | 13 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41-3589C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486114 | ||||||
chr17:45486125
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-41-3600C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486125 | ||||||
chr17:45486134
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-41-3609C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486134 | ||||||
chr17:45486149
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0192a0001c0001t0011g0191 | 3 | HG01358.hp1 HG03654.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-41-3624C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486149 | ||||||
chr17:45486160
|
T | G | 1 | a0001c0005t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-41-3635A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486160 | ||||||
chr17:45486183
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-3658G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486183 | ||||||
chr17:45486226
|
AAGATAAA others(10): Show |
A | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-41-3718_-41-3702d others(19): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486226 | ||||||
chr17:45486227
|
AG | A | 3 | a0001c0002t0002g0061a0001c0002t0002g0062a0001c0002t0002g0072 | 3 | HG01433.hp2 HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-41-3703delC | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486227 | ||||||
chr17:45486228
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-41-3703C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486228 | ||||||
chr17:45486230
|
T | A | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3705A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486230 | ||||||
chr17:45486235
|
T | A | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-3710A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486235 | ||||||
chr17:45486237
|
A | T | 1 | a0001c0002t0002g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-41-3712T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486237 | ||||||
chr17:45486240
|
A | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0102a0001c0001t0001g0194others(22): Show | 30 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-41-3715T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486240 | ||||||
chr17:45486243
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(157): Show | 204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.-41-3718A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486243 | ||||||
chr17:45486246
|
T | A | 18 | a0001c0001t0001g0024a0001c0001t0001g0076a0001c0001t0001g0091others(15): Show | 19 | HG00639.hp2 HG00735.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-41-3721A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486246 | ||||||
chr17:45486316
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-41-3791G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486316 | ||||||
chr17:45486353
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-41-3828G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486353 | ||||||
chr17:45486441
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-41-3916C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486441 | ||||||
chr17:45486504
|
G | A | 1 | a0001c0005t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-41-3979C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486504 | ||||||
chr17:45486528
|
T | C | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-41-4003A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486528 | ||||||
chr17:45486560
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-41-4035G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486560 | ||||||
chr17:45486573
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-41-4048G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486573 | ||||||
chr17:45486583
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA18966.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-41-4058T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486583 | ||||||
chr17:45486585
|
T | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-41-4060A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486585 | ||||||
chr17:45486586
|
T | A | 4 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(1): Show | 4 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-4061A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486586 | ||||||
chr17:45486856
|
T | G | 26 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(23): Show | 30 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-42+3796A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486856 | ||||||
chr17:45486991
|
C | T | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+3661G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45486991 | ||||||
chr17:45487131
|
G | A | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-42+3521C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487131 | ||||||
chr17:45487160
|
A | T | 1 | a0001c0005t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-42+3492T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487160 | ||||||
chr17:45487193
|
C | T | 3 | a0001c0004t0001g0048a0001c0004t0001g0049a0001c0004t0001g0050 | 3 | HG02717.hp2 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-42+3459G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487193 | ||||||
chr17:45487411
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-42+3241C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487411 | ||||||
chr17:45487744
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+2908C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45487744 | ||||||
chr17:45488057
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+2595C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488057 | ||||||
chr17:45488233
|
T | C | 21 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(18): Show | 24 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+2419A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488233 | ||||||
chr17:45488324
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(46): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-42+2328A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488324 | ||||||
chr17:45488409
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-42+2243T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488409 | ||||||
chr17:45488474
|
G | A | 22 | a0001c0001t0001g0076a0001c0002t0001g0074a0001c0002t0002g0009others(19): Show | 25 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-42+2178C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488474 | ||||||
chr17:45488495
|
T | G | 1 | a0001c0002t0002g0073 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-42+2157A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488495 | ||||||
chr17:45488540
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-42+2112T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488540 | ||||||
chr17:45488565
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0201a0001c0001t0001g0202 | 4 | HG00738.hp1 HG01943.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+2087T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488565 | ||||||
chr17:45488631
|
C | T | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-42+2021G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488631 | ||||||
chr17:45488640
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-42+2012A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488640 | ||||||
chr17:45488669
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-42+1983G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488669 | ||||||
chr17:45488680
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-42+1972G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488680 | ||||||
chr17:45488704
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-42+1948G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488704 | ||||||
chr17:45488796
|
G | A | 1 | a0001c0001t0003g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-42+1856C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488796 | ||||||
chr17:45488939
|
A | C | 1 | a0001c0001t0009g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-42+1713T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45488939 | ||||||
chr17:45489042
|
A | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 10 | HG01168.hp2 HG01169.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+1610T>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489042 | ||||||
chr17:45489063
|
GACTTGGG others(3): Show |
G | 1 | a0003c0007t0001g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-42+1579_-42+1588d others(12): Show |
PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489063 | ||||||
chr17:45489276
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+1376T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489276 | ||||||
chr17:45489322
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-42+1330A>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489322 | ||||||
chr17:45489328
|
G | A | 3 | a0001c0005t0001g0246a0001c0005t0001g0247a0001c0013t0001g0078 | 3 | HG02559.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+1324C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489328 | ||||||
chr17:45489565
|
A | G | 23 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0002t0001g0074others(20): Show | 26 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.-42+1087T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489565 | ||||||
chr17:45489600
|
G | A | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+1052C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489600 | ||||||
chr17:45489603
|
G | C | 6 | a0001c0001t0001g0053a0001c0004t0001g0048a0001c0004t0001g0049others(3): Show | 6 | HG02257.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+1049C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489603 | ||||||
chr17:45489618
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-42+1034C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489618 | ||||||
chr17:45489622
|
C | T | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+1030G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489622 | ||||||
chr17:45489623
|
C | G | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+1029G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489623 | ||||||
chr17:45489692
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-42+960T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489692 | ||||||
chr17:45489775
|
G | T | 1 | a0001c0005t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-42+877C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489775 | ||||||
chr17:45489781
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-42+871C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489781 | ||||||
chr17:45489809
|
T | G | 17 | a0001c0002t0002g0009a0001c0002t0002g0020a0001c0002t0002g0059others(14): Show | 20 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.-42+843A>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489809 | ||||||
chr17:45489828
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-42+824C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489828 | ||||||
chr17:45489855
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-42+797C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489855 | ||||||
chr17:45489941
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-42+711C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489941 | ||||||
chr17:45489961
|
T | A | 2 | a0001c0001t0001g0192a0001c0001t0011g0191 | 2 | HG01358.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-42+691A>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489961 | ||||||
chr17:45489971
|
C | G | 18 | a0001c0002t0001g0074a0001c0002t0002g0009a0001c0002t0002g0020others(15): Show | 21 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42+681G>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45489971 | ||||||
chr17:45490030
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-42+622G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490030 | ||||||
chr17:45490118
|
G | C | 3 | a0001c0001t0001g0055a0002c0003t0001g0008a0002c0003t0001g0054 | 5 | HG02896.hp2 HG02897.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+534C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490118 | ||||||
chr17:45490140
|
G | T | 4 | a0001c0001t0004g0018a0001c0001t0004g0040a0001c0001t0004g0041others(1): Show | 5 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+512C>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490140 | ||||||
chr17:45490179
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(179): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.-42+473T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490179 | ||||||
chr17:45490259
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-42+393C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490259 | ||||||
chr17:45490329
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-42+323C>T | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490329 | ||||||
chr17:45490341
|
G | C | 2 | a0001c0005t0001g0246a0001c0005t0001g0247 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-42+311C>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490341 | ||||||
chr17:45490360
|
A | C | 1 | a0001c0009t0012g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-42+292T>G | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490360 | ||||||
chr17:45490372
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-42+280T>C | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490372 | ||||||
chr17:45490641
|
C | T | 14 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 17 | HG01243.hp1 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42+11G>A | PLEKHM1 | ENSG00000225190.12 | transcript | ENST00000430334.8 | protein_coding | 1/11 | chr17 | 45490641 |