geneid | 5191 |
---|---|
ensemblid | ENSG00000112357.14 |
hgncid | 8860 |
symbol | PEX7 |
name | peroxisomal biogenesis factor 7 |
refseq_nuc | NM_000288.4 |
refseq_prot | NP_000279.1 |
ensembl_nuc | ENST00000318471.5 |
ensembl_prot | ENSP00000315680.3 |
mane_status | MANE Select |
chr | chr6 |
start | 136822592 |
end | 136913934 |
strand | + |
ver | v1.2 |
region | chr6:136822592-136913934 |
region5000 | chr6:136817592-136918934 |
regionname0 | PEX7_chr6_136822592_136913934 |
regionname5000 | PEX7_chr6_136817592_136918934 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 323 | 329 | 92 | 61 | 132 | 12 | 30 | 98 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0002 | 0/0 | 323 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 483 | 144 | 22 | 36 | 62 | 8 | 14 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0002 | 0/0 | 486 | 142 | 31 | 23 | 69 | 4 | 15 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0003 | 0/0 | 482 | 14 | 14 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0004 | 0/0 | 486 | 12 | 9 | 2 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0005 | 0/0 | 483 | 6 | 5 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0006 | 0/0 | 486 | 4 | 4 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0007 | 0/0 | 483 | 3 | 3 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0008 | 0/0 | 486 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0009 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0010 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
t0011 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 972 | 329 | 92 | 61 | 132 | 12 | 30 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0002c0002 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1454 | 144 | 22 | 36 | 62 | 8 | 14 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0002 | 0/0 | 1457 | 142 | 31 | 23 | 69 | 4 | 15 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0003 | 0/0 | 1453 | 14 | 14 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0004 | 0/0 | 1457 | 11 | 9 | 1 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0005 | 0/0 | 1454 | 6 | 5 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0006 | 0/0 | 1457 | 4 | 4 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0007 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0008 | 0/0 | 1457 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0009 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0010 | 0/0 | 1457 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0001c0001t0011 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
a0002c0002t0004 | 0/0 | 1457 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | copy fasta | chr6 | 136817592 | 136918934 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
a0002c0002t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01255 | hp2 | a0002 | c0002 | t0004 | g0150 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0292 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0288 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0153 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0311 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0112 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0316 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0312 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0149 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18947 | hp1 | a0001 | c0001 | t0010 | g0276 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | LWK | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | LWK | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | ASW | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ASW | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | TSI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | GIH | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | GIH | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0034 | REF | REF | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:136822793
|
C | T | 1 | a0002 | 1 | HG01255.hp2 | missense_variant&splice_region_variant | MODERATE | c.128C>T | p.Ala43Val | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | 202/1454 | 128/972 | 43/323 | chr6 | 136822793 | ||
chr6:136913929
|
AT | A | 1 | a0001 | 14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
splice_region_variant | LOW | c.*407delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 136913929 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:136822601
|
A | T | 1 | a0001c0001t0006 | 4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | chr6 | 136822601 | ||||||
chr6:136822610
|
C | T | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(4): Show | 38 | HG00639.hp2 HG01255.hp2 HG01884.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-56C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | 56 | chr6 | 136822610 | |||||
chr6:136822635
|
G | A | 2 | a0001c0001t0007a0001c0001t0008 | 5 | HG02622.hp1 HG02970.hp1 HG03139.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-31G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | 31 | chr6 | 136822635 | |||||
chr6:136913613
|
A | G | 1 | a0001c0001t0010 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | 87 | chr6 | 136913613 | |||||
chr6:136913781
|
T | TGTA | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(5): Show | 163 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*257_*258insAGT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | 258 | INFO_REALIGN_3_PRIME | chr6 | 136913781 | ||||
chr6:136913832
|
T | G | 6 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(3): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*306T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | 306 | chr6 | 136913832 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:136822842
|
G | GGGGGCC | 163 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.130+48_130+53dupGG others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 136822842 | |||||
chr6:136822888
|
C | T | 1 | a0001c0001t0002g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.130+93C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136822888 | ||||||
chr6:136822889
|
T | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+94T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136822889 | ||||||
chr6:136822946
|
C | T | 1 | a0001c0001t0006g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130+151C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136822946 | ||||||
chr6:136823011
|
C | A | 1 | a0001c0001t0002g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.130+216C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823011 | ||||||
chr6:136823080
|
G | C | 4 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014others(1): Show | 4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+285G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823080 | ||||||
chr6:136823105
|
G | A | 5 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+310G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823105 | ||||||
chr6:136823152
|
C | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.130+357C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823152 | ||||||
chr6:136823166
|
G | T | 1 | a0001c0001t0009g0156 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+371G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823166 | ||||||
chr6:136823217
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.130+422A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823217 | ||||||
chr6:136823306
|
C | T | 1 | a0001c0001t0009g0156 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+511C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823306 | ||||||
chr6:136823500
|
A | G | 167 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(164): Show | 171 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.130+705A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823500 | ||||||
chr6:136823614
|
C | G | 222 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0129others(219): Show | 230 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.130+819C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823614 | ||||||
chr6:136823688
|
C | A | 1 | a0001c0001t0002g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130+893C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823688 | ||||||
chr6:136823729
|
G | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.130+934G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823729 | ||||||
chr6:136823745
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.130+950C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823745 | ||||||
chr6:136823782
|
C | T | 156 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(153): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.130+987C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823782 | ||||||
chr6:136823847
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.130+1052G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823847 | ||||||
chr6:136824112
|
C | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.131-1102C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824112 | ||||||
chr6:136824112
|
C | G | 1 | a0001c0001t0002g0314 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.131-1102C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824112 | ||||||
chr6:136824538
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.131-676T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824538 | ||||||
chr6:136824589
|
A | G | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-625A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824589 | ||||||
chr6:136824623
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.131-591A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824623 | ||||||
chr6:136824675
|
A | G | 4 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014others(1): Show | 4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-539A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824675 | ||||||
chr6:136824939
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.131-275A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824939 | ||||||
chr6:136825045
|
A | G | 1 | a0001c0001t0009g0156 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-169A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136825045 | ||||||
chr6:136825504
|
T | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.188+233T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825504 | ||||||
chr6:136825524
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188+253C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825524 | ||||||
chr6:136825673
|
A | G | 1 | a0001c0001t0002g0313 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.188+402A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825673 | ||||||
chr6:136825806
|
T | G | 1 | a0001c0001t0002g0314 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.189-513T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825806 | ||||||
chr6:136825813
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189-506G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825813 | ||||||
chr6:136826244
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.189-75A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136826244 | ||||||
chr6:136826292
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189-27T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136826292 | ||||||
chr6:136826553
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.339+84A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826553 | ||||||
chr6:136826577
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01496.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.339+108C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826577 | ||||||
chr6:136826635
|
G | A | 24 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(21): Show | 27 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.339+166G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826635 | ||||||
chr6:136826892
|
A | G | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+423A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826892 | ||||||
chr6:136826922
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.339+453T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826922 | ||||||
chr6:136827144
|
T | A | 1 | a0001c0001t0002g0144 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.339+675T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827144 | ||||||
chr6:136827182
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.339+713A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827182 | ||||||
chr6:136827238
|
G | T | 4 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0312others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+769G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827238 | ||||||
chr6:136827370
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.339+901A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827370 | ||||||
chr6:136827388
|
T | C | 1 | a0001c0001t0002g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.339+919T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827388 | ||||||
chr6:136827392
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.339+923T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827392 | ||||||
chr6:136827504
|
T | TTG | 23 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0039others(20): Show | 25 | HG00323.hp1 HG00597.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.339+1079_339+1080d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
T | TTGTG | 34 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(31): Show | 36 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.339+1077_339+1080d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
T | TTGTGTG | 17 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0084others(14): Show | 18 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.339+1075_339+1080d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
T | TTGTGTGT others(1): Show |
10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.339+1073_339+1080d others(10): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
TTG | T | 32 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(29): Show | 35 | HG00639.hp2 HG01169.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.339+1079_339+1080d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
TTGTG | T | 14 | a0001c0001t0001g0129a0001c0001t0001g0176a0001c0001t0001g0177others(11): Show | 14 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.339+1077_339+1080d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
TTGTGTG | T | 10 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(7): Show | 10 | HG02027.hp1 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+1075_339+1080d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
TTGTGTGT others(1): Show |
T | 16 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(13): Show | 16 | HG01106.hp2 HG01433.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.339+1073_339+1080d others(10): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
TTGTGTGT others(3): Show |
T | 122 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.339+1071_339+1080d others(12): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
TTGTGTGT others(5): Show |
T | 12 | a0001c0001t0002g0188a0001c0001t0002g0196a0001c0001t0002g0197others(9): Show | 12 | HG01106.hp1 HG01192.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.339+1069_339+1080d others(14): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827504
|
TTGTGTGT others(7): Show |
T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.339+1067_339+1080d others(16): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | |||||
chr6:136827657
|
C | T | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+1188C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827657 | ||||||
chr6:136827687
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.339+1218C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827687 | ||||||
chr6:136827766
|
A | G | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+1297A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827766 | ||||||
chr6:136827776
|
C | G | 2 | a0001c0001t0002g0142a0001c0001t0002g0143 | 2 | NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.339+1307C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827776 | ||||||
chr6:136827951
|
T | G | 1 | a0001c0001t0002g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.339+1482T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827951 | ||||||
chr6:136828073
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.339+1604A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828073 | ||||||
chr6:136828093
|
G | T | 191 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(188): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.339+1624G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828093 | ||||||
chr6:136828139
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.339+1670A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828139 | ||||||
chr6:136828304
|
A | G | 24 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(21): Show | 27 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.339+1835A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828304 | ||||||
chr6:136828399
|
T | C | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+1930T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828399 | ||||||
chr6:136828435
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.339+1966G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828435 | ||||||
chr6:136828457
|
A | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0299 | 3 | HG02056.hp2 NA18612.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.339+1988A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828457 | ||||||
chr6:136828534
|
G | T | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.339+2065G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828534 | ||||||
chr6:136828627
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.339+2158C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828627 | ||||||
chr6:136828628
|
G | C | 5 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+2159G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828628 | ||||||
chr6:136828765
|
C | T | 5 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+2296C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828765 | ||||||
chr6:136828892
|
A | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.339+2423A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828892 | ||||||
chr6:136828949
|
A | G | 1 | a0001c0001t0008g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.339+2480A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828949 | ||||||
chr6:136829024
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+2555A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829024 | ||||||
chr6:136829026
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.339+2557C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829026 | ||||||
chr6:136829273
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.339+2804T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829273 | ||||||
chr6:136829305
|
GC | G | 5 | a0001c0001t0001g0295a0001c0001t0002g0292a0001c0001t0002g0293others(2): Show | 5 | HG01243.hp1 HG01433.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2839delC | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136829305 | |||||
chr6:136829309
|
A | T | 5 | a0001c0001t0001g0295a0001c0001t0002g0292a0001c0001t0002g0293others(2): Show | 5 | HG01243.hp1 HG01433.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2840A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829309 | ||||||
chr6:136829356
|
G | A | 224 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(221): Show | 232 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.339+2887G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829356 | ||||||
chr6:136829405
|
T | C | 206 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(203): Show | 213 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.339+2936T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829405 | ||||||
chr6:136829566
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.339+3097C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829566 | ||||||
chr6:136829597
|
A | G | 5 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+3128A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829597 | ||||||
chr6:136829757
|
C | T | 1 | a0001c0001t0008g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.339+3288C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829757 | ||||||
chr6:136829758
|
G | A | 23 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(20): Show | 26 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+3289G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829758 | ||||||
chr6:136829987
|
G | GT | 6 | a0001c0001t0001g0187a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG01256.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+3530dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136829987 | |||||
chr6:136829987
|
GT | G | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+3530delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136829987 | |||||
chr6:136829988
|
T | G | 1 | a0001c0001t0008g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.339+3519T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829988 | ||||||
chr6:136830041
|
G | T | 6 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0141others(3): Show | 6 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+3572G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830041 | ||||||
chr6:136830123
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.339+3654A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830123 | ||||||
chr6:136830160
|
G | A | 9 | a0001c0001t0001g0136a0001c0001t0004g0147a0001c0001t0004g0148others(6): Show | 9 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.339+3691G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830160 | ||||||
chr6:136830630
|
A | G | 4 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014others(1): Show | 4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+4161A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830630 | ||||||
chr6:136830693
|
T | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.339+4224T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830693 | ||||||
chr6:136830878
|
CAT | C | 4 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0312others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+4412_339+4413d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136830878 | |||||
chr6:136830970
|
T | G | 2 | a0001c0001t0002g0196a0001c0001t0002g0203 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.339+4501T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830970 | ||||||
chr6:136831076
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.339+4607G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831076 | ||||||
chr6:136831369
|
C | T | 198 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(195): Show | 205 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.339+4900C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831369 | ||||||
chr6:136831483
|
T | C | 211 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(208): Show | 218 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.339+5014T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831483 | ||||||
chr6:136831531
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.339+5062C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831531 | ||||||
chr6:136831565
|
A | G | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.339+5096A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831565 | ||||||
chr6:136831646
|
A | G | 5 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+5177A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831646 | ||||||
chr6:136831719
|
G | A | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+5250G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831719 | ||||||
chr6:136831796
|
T | A | 1 | a0001c0001t0001g0300 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.339+5327T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831796 | ||||||
chr6:136831798
|
C | G | 1 | a0001c0001t0002g0307 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339+5329C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831798 | ||||||
chr6:136831908
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.339+5439G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831908 | ||||||
chr6:136831934
|
G | A | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.339+5465G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831934 | ||||||
chr6:136832048
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.339+5579T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832048 | ||||||
chr6:136832192
|
T | C | 206 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(203): Show | 213 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.339+5723T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832192 | ||||||
chr6:136832221
|
T | C | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG00741.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.339+5752T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832221 | ||||||
chr6:136832449
|
T | C | 6 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+5980T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832449 | ||||||
chr6:136832517
|
T | G | 158 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(155): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.339+6048T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832517 | ||||||
chr6:136832560
|
G | C | 1 | a0001c0001t0001g0054 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.339+6091G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832560 | ||||||
chr6:136832667
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.339+6198C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832667 | ||||||
chr6:136832668
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.339+6199G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832668 | ||||||
chr6:136832723
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.339+6254A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832723 | ||||||
chr6:136832836
|
C | T | 158 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(155): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.339+6367C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832836 | ||||||
chr6:136832912
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0026others(5): Show | 10 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.339+6443T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832912 | ||||||
chr6:136833231
|
G | C | 3 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209 | 3 | HG02074.hp1 NA18944.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.339+6762G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833231 | ||||||
chr6:136833268
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.339+6799C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833268 | ||||||
chr6:136833388
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.339+6919G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833388 | ||||||
chr6:136833460
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.339+6991T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833460 | ||||||
chr6:136833482
|
G | A | 225 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(222): Show | 233 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.339+7013G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833482 | ||||||
chr6:136833804
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339+7335A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833804 | ||||||
chr6:136833889
|
T | C | 23 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(20): Show | 26 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+7420T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833889 | ||||||
chr6:136834023
|
A | C | 1 | a0001c0001t0002g0307 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339+7554A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834023 | ||||||
chr6:136834028
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.339+7559A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834028 | ||||||
chr6:136834045
|
C | T | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+7576C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834045 | ||||||
chr6:136834094
|
C | A | 1 | a0001c0001t0001g0008 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.339+7625C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834094 | ||||||
chr6:136834108
|
A | C | 5 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+7639A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834108 | ||||||
chr6:136834215
|
TG | T | 7 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+7748delG | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136834215 | |||||
chr6:136834361
|
C | T | 192 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(189): Show | 199 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.339+7892C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834361 | ||||||
chr6:136834419
|
G | C | 23 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(20): Show | 26 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+7950G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834419 | ||||||
chr6:136834548
|
T | A | 30 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0003g0004others(27): Show | 33 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.339+8079T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834548 | ||||||
chr6:136834586
|
A | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+8117A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834586 | ||||||
chr6:136834625
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.339+8156T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834625 | ||||||
chr6:136834672
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.339+8203C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834672 | ||||||
chr6:136834704
|
T | C | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0183others(12): Show | 15 | HG01255.hp2 HG01981.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.339+8235T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834704 | ||||||
chr6:136834788
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0078others(3): Show | 6 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+8319C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834788 | ||||||
chr6:136835004
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.339+8535A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835004 | ||||||
chr6:136835020
|
A | G | 1 | a0001c0001t0006g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+8551A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835020 | ||||||
chr6:136835125
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.339+8656G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835125 | ||||||
chr6:136835285
|
T | A | 2 | a0001c0001t0003g0108a0001c0001t0003g0109 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.339+8816T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835285 | ||||||
chr6:136835382
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.339+8913G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835382 | ||||||
chr6:136835549
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.339+9080A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835549 | ||||||
chr6:136835559
|
T | A | 4 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014others(1): Show | 4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+9090T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835559 | ||||||
chr6:136835788
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0002g0286a0001c0001t0008g0128 | 3 | HG01256.hp2 HG01358.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.339+9319A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835788 | ||||||
chr6:136835875
|
A | C | 4 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014others(1): Show | 4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+9406A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835875 | ||||||
chr6:136836052
|
T | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.340-9563T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836052 | ||||||
chr6:136836142
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.340-9473T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836142 | ||||||
chr6:136836233
|
AAG | A | 195 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(192): Show | 202 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.340-9377_340-9376d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136836233 | |||||
chr6:136836297
|
A | T | 1 | a0001c0001t0001g0027 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.340-9318A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836297 | ||||||
chr6:136836446
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.340-9169C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836446 | ||||||
chr6:136836483
|
C | T | 1 | a0001c0001t0002g0285 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.340-9132C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836483 | ||||||
chr6:136836621
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.340-8994T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836621 | ||||||
chr6:136836724
|
G | A | 26 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0003g0004others(23): Show | 29 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.340-8891G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836724 | ||||||
chr6:136836869
|
C | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.340-8746C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836869 | ||||||
chr6:136836900
|
T | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0081 | 3 | HG01358.hp1 HG01981.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.340-8715T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836900 | ||||||
chr6:136837009
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.340-8606C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837009 | ||||||
chr6:136837112
|
G | A | 4 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(1): Show | 4 | HG02630.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-8503G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837112 | ||||||
chr6:136837279
|
G | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0008g0015 | 3 | HG02622.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.340-8336G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837279 | ||||||
chr6:136837317
|
G | A | 6 | a0001c0001t0001g0129a0001c0001t0002g0182a0001c0001t0007g0012others(3): Show | 6 | HG02622.hp1 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-8298G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837317 | ||||||
chr6:136837341
|
G | A | 1 | a0001c0001t0002g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.340-8274G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837341 | ||||||
chr6:136837361
|
C | CA | 14 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG02155.hp2 NA18612.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.340-8240dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAA | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-8243_340-8240d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAA | 21 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(18): Show | 24 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.340-8245_340-8240d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0137a0001c0001t0002g0186 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.340-8249_340-8240d others(12): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.340-8250_340-8240d others(13): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(3): Show | 6 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-8251_340-8240d others(14): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0008g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.340-8252_340-8240d others(15): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0171a0001c0001t0001g0295a0001c0001t0002g0145others(5): Show | 8 | HG01257.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-8253_340-8240d others(16): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(8): Show |
122 | a0001c0001t0001g0008a0001c0001t0001g0129a0001c0001t0001g0161others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.340-8240_340-8239i others(17): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(9): Show |
29 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0160others(26): Show | 29 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.340-8240_340-8239i others(18): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837361
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.340-8240_340-8239i others(19): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | |||||
chr6:136837391
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.340-8224A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837391 | ||||||
chr6:136837506
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0002g0130 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.340-8109T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837506 | ||||||
chr6:136837530
|
T | C | 25 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.340-8085T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837530 | ||||||
chr6:136837626
|
G | C | 198 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(195): Show | 205 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.340-7989G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837626 | ||||||
chr6:136837695
|
A | G | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG00423.hp2 HG00597.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-7920A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837695 | ||||||
chr6:136837738
|
C | T | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-7877C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837738 | ||||||
chr6:136837812
|
C | CCA | 22 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(19): Show | 22 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.340-7771_340-7770d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | |||||
chr6:136837812
|
C | CCACA | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0035others(34): Show | 40 | HG00639.hp2 HG01081.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.340-7773_340-7770d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | |||||
chr6:136837812
|
CCA | C | 72 | a0001c0001t0001g0106a0001c0001t0001g0159a0001c0001t0001g0160others(69): Show | 74 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.340-7771_340-7770d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | |||||
chr6:136837812
|
CCACACA | C | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-7775_340-7770d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | |||||
chr6:136837813
|
C | T | 23 | a0001c0001t0002g0170a0001c0001t0002g0188a0001c0001t0002g0200others(20): Show | 23 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.340-7802C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837813 | ||||||
chr6:136837815
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.340-7800C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837815 | ||||||
chr6:136837869
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.340-7746G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837869 | ||||||
chr6:136838222
|
A | G | 12 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-7393A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838222 | ||||||
chr6:136838498
|
C | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0004g0151 | 3 | HG02559.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.340-7117C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838498 | ||||||
chr6:136838543
|
C | A | 3 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0139 | 3 | HG04204.hp1 NA18942.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.340-7072C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838543 | ||||||
chr6:136838964
|
A | G | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.340-6651A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838964 | ||||||
chr6:136839060
|
G | T | 2 | a0001c0001t0004g0116a0001c0001t0004g0117 | 2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.340-6555G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839060 | ||||||
chr6:136839061
|
G | T | 2 | a0001c0001t0004g0116a0001c0001t0004g0117 | 2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.340-6554G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839061 | ||||||
chr6:136839244
|
T | A | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.340-6371T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839244 | ||||||
chr6:136839273
|
C | G | 1 | a0001c0001t0001g0047 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.340-6342C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839273 | ||||||
chr6:136839364
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.340-6251G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839364 | ||||||
chr6:136839368
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-6247A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839368 | ||||||
chr6:136839414
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.340-6201G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839414 | ||||||
chr6:136839639
|
T | A | 1 | a0001c0001t0002g0207 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.340-5976T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839639 | ||||||
chr6:136839677
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-5938G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839677 | ||||||
chr6:136839712
|
A | G | 12 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-5903A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839712 | ||||||
chr6:136839837
|
A | G | 1 | a0001c0001t0002g0283 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.340-5778A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839837 | ||||||
chr6:136839845
|
A | G | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.340-5770A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839845 | ||||||
chr6:136840214
|
A | C | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-5401A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840214 | ||||||
chr6:136840368
|
T | C | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-5247T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840368 | ||||||
chr6:136840409
|
G | A | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-5206G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840409 | ||||||
chr6:136840455
|
A | T | 1 | a0001c0001t0002g0296 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.340-5160A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840455 | ||||||
chr6:136840508
|
T | TGTA | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.340-5106_340-5105i others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136840508 | |||||
chr6:136840533
|
C | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.340-5082C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840533 | ||||||
chr6:136841084
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.340-4531C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841084 | ||||||
chr6:136841159
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0081 | 3 | HG01358.hp1 HG01981.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.340-4456G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841159 | ||||||
chr6:136841161
|
G | C | 122 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(119): Show | 125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.340-4454G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841161 | ||||||
chr6:136841390
|
A | C | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-4225A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841390 | ||||||
chr6:136841394
|
C | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-4221C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841394 | ||||||
chr6:136841413
|
A | G | 20 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0084others(17): Show | 23 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.340-4202A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841413 | ||||||
chr6:136841535
|
T | C | 1 | a0001c0001t0002g0314 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.340-4080T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841535 | ||||||
chr6:136841620
|
C | G | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.340-3995C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841620 | ||||||
chr6:136841774
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.340-3841G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841774 | ||||||
chr6:136841824
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(211): Show | 221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.340-3791G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841824 | ||||||
chr6:136841849
|
G | A | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0114others(12): Show | 15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340-3766G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841849 | ||||||
chr6:136841876
|
G | A | 213 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(210): Show | 220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.340-3739G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841876 | ||||||
chr6:136841904
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.340-3711A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841904 | ||||||
chr6:136841907
|
A | T | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-3708A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841907 | ||||||
chr6:136842002
|
C | CT | 20 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(17): Show | 20 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.340-3599dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136842002 | |||||
chr6:136842275
|
G | C | 1 | a0001c0001t0003g0004 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.340-3340G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842275 | ||||||
chr6:136842285
|
A | G | 211 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(208): Show | 218 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.340-3330A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842285 | ||||||
chr6:136842308
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 7 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-3307A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842308 | ||||||
chr6:136842466
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.340-3149T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842466 | ||||||
chr6:136842481
|
C | T | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-3134C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842481 | ||||||
chr6:136842586
|
A | AT | 3 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0308 | 3 | HG01243.hp1 HG01433.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.340-3026dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136842586 | |||||
chr6:136842761
|
G | C | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-2854G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842761 | ||||||
chr6:136843021
|
G | A | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-2594G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843021 | ||||||
chr6:136843275
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.340-2340A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843275 | ||||||
chr6:136843444
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.340-2171G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843444 | ||||||
chr6:136843458
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.340-2157G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843458 | ||||||
chr6:136843484
|
G | T | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.340-2131G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843484 | ||||||
chr6:136843660
|
T | C | 165 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(162): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.340-1955T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843660 | ||||||
chr6:136843699
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.340-1916C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843699 | ||||||
chr6:136843861
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.340-1754G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843861 | ||||||
chr6:136843914
|
C | T | 7 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0139others(4): Show | 7 | HG02027.hp1 HG04204.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1701C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843914 | ||||||
chr6:136843994
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0072others(2): Show | 5 | HG00544.hp2 HG00558.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-1621A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843994 | ||||||
chr6:136844092
|
C | T | 12 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-1523C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844092 | ||||||
chr6:136844111
|
A | T | 213 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(210): Show | 220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.340-1504A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844111 | ||||||
chr6:136844135
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0002g0309 | 2 | NA18960.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.340-1480C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844135 | ||||||
chr6:136844349
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.340-1266C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844349 | ||||||
chr6:136844372
|
G | GA | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-1232dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136844372 | |||||
chr6:136844372
|
GA | G | 122 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(119): Show | 125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.340-1232delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136844372 | |||||
chr6:136844577
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.340-1038A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844577 | ||||||
chr6:136844614
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.340-1001T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844614 | ||||||
chr6:136844795
|
C | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0203 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.340-820C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844795 | ||||||
chr6:136844808
|
A | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-807A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844808 | ||||||
chr6:136844817
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.340-798C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844817 | ||||||
chr6:136845087
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.340-528G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845087 | ||||||
chr6:136845129
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-486T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845129 | ||||||
chr6:136845333
|
G | A | 17 | a0001c0001t0002g0009a0001c0001t0002g0154a0001c0001t0002g0197others(14): Show | 18 | HG00544.hp1 HG01169.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-282G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845333 | ||||||
chr6:136845507
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.340-108G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845507 | ||||||
chr6:136845512
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-103A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845512 | ||||||
chr6:136845544
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(310): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.340-71G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845544 | ||||||
chr6:136845720
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.417+28C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 4/9 | chr6 | 136845720 | ||||||
chr6:136845839
|
G | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.417+147G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 4/9 | chr6 | 136845839 | ||||||
chr6:136846195
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+14T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846195 | ||||||
chr6:136846225
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.526+44G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846225 | ||||||
chr6:136846256
|
G | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0186 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526+75G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846256 | ||||||
chr6:136846287
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+106A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846287 | ||||||
chr6:136846307
|
T | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+126T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846307 | ||||||
chr6:136846337
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.526+156T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846337 | ||||||
chr6:136846338
|
A | C | 1 | a0001c0001t0002g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.526+157A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846338 | ||||||
chr6:136846338
|
A | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0081 | 2 | HG01981.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.526+157A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846338 | ||||||
chr6:136846345
|
T | A | 1 | a0001c0001t0002g0307 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526+164T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846345 | ||||||
chr6:136846388
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.526+207A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846388 | ||||||
chr6:136846588
|
G | A | 4 | a0001c0001t0006g0310a0001c0001t0006g0311a0001c0001t0006g0312others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+407G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846588 | ||||||
chr6:136846589
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526+408C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846589 | ||||||
chr6:136846607
|
C | G | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.526+426C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846607 | ||||||
chr6:136846696
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.526+515G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846696 | ||||||
chr6:136846793
|
G | A | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.526+612G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846793 | ||||||
chr6:136846906
|
G | A | 164 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.526+725G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846906 | ||||||
chr6:136847026
|
T | C | 9 | a0001c0001t0002g0305a0001c0001t0004g0147a0001c0001t0004g0148others(6): Show | 9 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.526+845T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847026 | ||||||
chr6:136847043
|
G | A | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+862G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847043 | ||||||
chr6:136847120
|
GTTGGCTG others(4652): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.526+981_526+5639de others(1): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136847120 | |||||
chr6:136847212
|
GTT | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(312): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.526+1035_526+1036d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136847212 | |||||
chr6:136847287
|
C | T | 184 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(181): Show | 188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.526+1106C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847287 | ||||||
chr6:136847342
|
A | T | 122 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(119): Show | 125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.526+1161A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847342 | ||||||
chr6:136847395
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526+1214T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847395 | ||||||
chr6:136847438
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+1257G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847438 | ||||||
chr6:136847590
|
A | G | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+1409A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847590 | ||||||
chr6:136847663
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.526+1482G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847663 | ||||||
chr6:136847952
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526+1771C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847952 | ||||||
chr6:136848071
|
A | T | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+1890A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848071 | ||||||
chr6:136848130
|
G | T | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+1949G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848130 | ||||||
chr6:136848143
|
T | G | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+1962T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848143 | ||||||
chr6:136848260
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 6 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+2079T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848260 | ||||||
chr6:136848290
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(143): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.526+2109A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848290 | ||||||
chr6:136848364
|
A | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+2183A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848364 | ||||||
chr6:136848530
|
A | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+2349A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848530 | ||||||
chr6:136848531
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG01081.hp2 HG01123.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.526+2350C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848531 | ||||||
chr6:136848559
|
AG | A | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0002c0002t0004g0150 | 3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.526+2381delG | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136848559 | |||||
chr6:136848561
|
G | C | 23 | a0001c0001t0002g0170a0001c0001t0002g0204a0001c0001t0002g0205others(20): Show | 23 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+2380G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848561 | ||||||
chr6:136848561
|
G | T | 6 | a0001c0001t0002g0188a0001c0001t0002g0198a0001c0001t0002g0200others(3): Show | 6 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+2380G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848561 | ||||||
chr6:136848663
|
T | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+2482T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848663 | ||||||
chr6:136848710
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526+2529T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848710 | ||||||
chr6:136848780
|
A | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.526+2599A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848780 | ||||||
chr6:136848795
|
A | G | 29 | a0001c0001t0002g0170a0001c0001t0002g0188a0001c0001t0002g0198others(26): Show | 29 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.526+2614A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848795 | ||||||
chr6:136848837
|
C | G | 1 | a0001c0001t0002g0315 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.526+2656C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848837 | ||||||
chr6:136848850
|
A | G | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+2669A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848850 | ||||||
chr6:136848888
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526+2707G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848888 | ||||||
chr6:136849010
|
T | A | 1 | a0001c0001t0002g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.526+2829T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849010 | ||||||
chr6:136849013
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0002g0130 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.526+2832T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849013 | ||||||
chr6:136849168
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.526+2987G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849168 | ||||||
chr6:136849172
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.526+2991T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849172 | ||||||
chr6:136849324
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.526+3143T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849324 | ||||||
chr6:136849331
|
G | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+3150G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849331 | ||||||
chr6:136849352
|
T | C | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0008g0128 | 3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.526+3171T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849352 | ||||||
chr6:136849468
|
C | T | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.526+3287C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849468 | ||||||
chr6:136849494
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0317 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.526+3313C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849494 | ||||||
chr6:136849510
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.526+3329A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849510 | ||||||
chr6:136849618
|
G | T | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+3437G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849618 | ||||||
chr6:136849870
|
T | C | 195 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(192): Show | 199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.526+3689T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849870 | ||||||
chr6:136850026
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.526+3845T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850026 | ||||||
chr6:136850064
|
T | G | 1 | a0001c0001t0001g0039 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.526+3883T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850064 | ||||||
chr6:136850184
|
C | CT | 10 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0004g0147others(7): Show | 10 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+4013dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850184 | |||||
chr6:136850195
|
G | A | 1 | a0001c0001t0002g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.526+4014G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850195 | ||||||
chr6:136850233
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.526+4052A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850233 | ||||||
chr6:136850268
|
G | A | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.526+4087G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850268 | ||||||
chr6:136850293
|
G | C | 20 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0145others(17): Show | 20 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.526+4112G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850293 | ||||||
chr6:136850455
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0238 | 2 | HG02083.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.526+4274G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850455 | ||||||
chr6:136850488
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.526+4307G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850488 | ||||||
chr6:136850497
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.526+4316C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850497 | ||||||
chr6:136850603
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.526+4422C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850603 | ||||||
chr6:136850640
|
G | C | 1 | a0001c0001t0002g0242 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.526+4459G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850640 | ||||||
chr6:136850741
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.526+4560G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850741 | ||||||
chr6:136850742
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.526+4561C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850742 | ||||||
chr6:136850833
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.526+4652A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850833 | ||||||
chr6:136850917
|
G | GT | 30 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 33 | HG00140.hp1 HG00544.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.526+4757dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | |||||
chr6:136850917
|
G | GTT | 30 | a0001c0001t0001g0102a0001c0001t0001g0160a0001c0001t0001g0161others(27): Show | 30 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.526+4756_526+4757d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | |||||
chr6:136850917
|
G | GTTT | 11 | a0001c0001t0001g0159a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG01255.hp1 HG01258.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+4755_526+4757d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | |||||
chr6:136850917
|
GT | G | 53 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0040others(50): Show | 56 | HG00423.hp1 HG00438.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.526+4757delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | |||||
chr6:136850917
|
GTT | G | 82 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(79): Show | 85 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.526+4756_526+4757d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | |||||
chr6:136850917
|
GTTT | G | 10 | a0001c0001t0002g0182a0001c0001t0002g0210a0001c0001t0002g0224others(7): Show | 10 | HG00099.hp1 HG01169.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.526+4755_526+4757d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | |||||
chr6:136850927
|
T | TG | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+4746_526+4747i others(3): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850927 | ||||||
chr6:136850969
|
CT | C | 13 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0180others(10): Show | 13 | HG00558.hp2 HG02027.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.526+4798delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850969 | |||||
chr6:136850979
|
T | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+4798T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850979 | ||||||
chr6:136850980
|
AT | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 8 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+4809delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850980 | |||||
chr6:136850998
|
A | AT | 146 | a0001c0001t0001g0158a0001c0001t0001g0189a0001c0001t0002g0009others(143): Show | 149 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.526+4831dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850998 | |||||
chr6:136850998
|
A | ATT | 6 | a0001c0001t0001g0157a0001c0001t0002g0145a0001c0001t0002g0146others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+4830_526+4831d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850998 | |||||
chr6:136850998
|
AT | A | 14 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG02155.hp2 HG03139.hp1 HG03516.hp2 others(11): Show |
intron_variant | MODIFIER | c.526+4831delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850998 | |||||
chr6:136851149
|
C | A | 12 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+4968C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851149 | ||||||
chr6:136851221
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+5040A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851221 | ||||||
chr6:136851335
|
A | C | 3 | a0001c0001t0002g0264a0001c0001t0002g0294a0001c0001t0002g0308 | 3 | HG01433.hp2 HG03654.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.526+5154A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851335 | ||||||
chr6:136851365
|
G | T | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+5184G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851365 | ||||||
chr6:136851435
|
A | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0223 | 3 | HG00140.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.526+5254A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851435 | ||||||
chr6:136851450
|
G | A | 1 | a0001c0001t0002g0244 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.526+5269G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851450 | ||||||
chr6:136851570
|
T | C | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0002g0202others(1): Show | 4 | HG02572.hp1 NA18956.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+5389T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851570 | ||||||
chr6:136851582
|
T | A | 1 | a0001c0001t0005g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.526+5401T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851582 | ||||||
chr6:136851755
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.526+5574T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851755 | ||||||
chr6:136851784
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.526+5603C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851784 | ||||||
chr6:136851874
|
T | G | 7 | a0001c0001t0001g0093a0001c0001t0002g0245a0001c0001t0003g0108others(4): Show | 7 | HG00642.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+5693T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851874 | ||||||
chr6:136851883
|
T | C | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+5702T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851883 | ||||||
chr6:136851895
|
A | T | 1 | a0001c0001t0002g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526+5714A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851895 | ||||||
chr6:136851942
|
G | T | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+5761G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851942 | ||||||
chr6:136851944
|
T | C | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+5763T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851944 | ||||||
chr6:136851945
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+5764G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851945 | ||||||
chr6:136851998
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.526+5817G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851998 | ||||||
chr6:136852000
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+5819G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852000 | ||||||
chr6:136852040
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0050others(5): Show | 10 | NA18949.hp2 NA18960.hp1 NA18973.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+5859C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852040 | ||||||
chr6:136852060
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(211): Show | 221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.526+5879G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852060 | ||||||
chr6:136852083
|
G | A | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.526+5902G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852083 | ||||||
chr6:136852180
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526+5999A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852180 | ||||||
chr6:136852388
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.526+6207C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852388 | ||||||
chr6:136852497
|
G | A | 12 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+6316G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852497 | ||||||
chr6:136852506
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+6325T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852506 | ||||||
chr6:136852560
|
A | G | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0114others(12): Show | 15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+6379A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852560 | ||||||
chr6:136852714
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+6533T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852714 | ||||||
chr6:136852891
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.526+6710C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852891 | ||||||
chr6:136852892
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.526+6711A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852892 | ||||||
chr6:136852930
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.526+6749C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852930 | ||||||
chr6:136852965
|
A | C | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+6784A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852965 | ||||||
chr6:136853006
|
A | G | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+6825A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853006 | ||||||
chr6:136853121
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+6940A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853121 | ||||||
chr6:136853284
|
C | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+7103C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853284 | ||||||
chr6:136853407
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+7226G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853407 | ||||||
chr6:136853416
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.526+7235C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853416 | ||||||
chr6:136853474
|
C | CT | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+7294dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136853474 | |||||
chr6:136853567
|
C | T | 146 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(143): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.526+7386C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853567 | ||||||
chr6:136854017
|
T | C | 4 | a0001c0001t0002g0204a0001c0001t0002g0220a0001c0001t0002g0270others(1): Show | 4 | HG01952.hp2 HG02004.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+7836T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854017 | ||||||
chr6:136854080
|
CTTTACGG others(3): Show |
C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+7900_526+7909d others(12): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854080 | ||||||
chr6:136854133
|
A | G | 11 | a0001c0001t0002g0144a0001c0001t0002g0190a0001c0001t0002g0191others(8): Show | 11 | HG02015.hp2 HG02083.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+7952A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854133 | ||||||
chr6:136854220
|
A | G | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0002c0002t0004g0150 | 3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.526+8039A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854220 | ||||||
chr6:136854344
|
A | G | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+8163A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854344 | ||||||
chr6:136854603
|
G | A | 1 | a0001c0001t0010g0276 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.526+8422G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854603 | ||||||
chr6:136854626
|
A | G | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+8445A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854626 | ||||||
chr6:136854643
|
C | T | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(5): Show | 8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+8462C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854643 | ||||||
chr6:136854677
|
T | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+8496T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854677 | ||||||
chr6:136854756
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526+8575C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854756 | ||||||
chr6:136854947
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+8766G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854947 | ||||||
chr6:136854952
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.526+8771G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854952 | ||||||
chr6:136854993
|
C | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0026others(4): Show | 9 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+8812C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854993 | ||||||
chr6:136854995
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.526+8814G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854995 | ||||||
chr6:136855051
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+8870G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855051 | ||||||
chr6:136855085
|
C | CA | 5 | a0001c0001t0001g0008a0001c0001t0001g0223a0001c0001t0004g0148others(2): Show | 6 | HG00140.hp1 HG01255.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+8917dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136855085 | |||||
chr6:136855210
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.526+9029A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855210 | ||||||
chr6:136855347
|
C | CT | 37 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0157others(34): Show | 37 | HG00639.hp2 HG01081.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.526+9180dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136855347 | |||||
chr6:136855405
|
T | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.526+9224T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855405 | ||||||
chr6:136855427
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.526+9246C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855427 | ||||||
chr6:136855582
|
C | T | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+9401C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855582 | ||||||
chr6:136855746
|
C | T | 117 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(114): Show | 120 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.526+9565C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855746 | ||||||
chr6:136855836
|
T | C | 2 | a0001c0001t0002g0142a0001c0001t0002g0143 | 2 | NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.526+9655T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855836 | ||||||
chr6:136855981
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0084 | 3 | HG03130.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.526+9800C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855981 | ||||||
chr6:136856034
|
A | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.526+9853A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856034 | ||||||
chr6:136856291
|
T | TA | 27 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0074others(24): Show | 28 | HG00544.hp2 HG01123.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.526+10136dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856291 | |||||
chr6:136856291
|
TA | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0086others(35): Show | 39 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.526+10136delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856291 | |||||
chr6:136856465
|
A | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-10162A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856465 | ||||||
chr6:136856562
|
G | GT | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-10062dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856562 | |||||
chr6:136856793
|
C | T | 1 | a0001c0001t0002g0313 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.527-9834C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856793 | ||||||
chr6:136856908
|
A | G | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-9719A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856908 | ||||||
chr6:136856910
|
A | ACAGTAAA others(333): Show |
1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.527-9702_527-9701i others(342): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856910 | |||||
chr6:136856910
|
A | ACAGTAAA others(350): Show |
1 | a0001c0001t0001g0133 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.527-9702_527-9701i others(359): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856910 | |||||
chr6:136857050
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.527-9577T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857050 | ||||||
chr6:136857316
|
A | T | 220 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(217): Show | 228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.527-9311A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857316 | ||||||
chr6:136857482
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.527-9145C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857482 | ||||||
chr6:136857686
|
CT | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8939delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136857686 | |||||
chr6:136857705
|
T | A | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.527-8922T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857705 | ||||||
chr6:136857863
|
C | A | 5 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0110others(2): Show | 5 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-8764C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857863 | ||||||
chr6:136857962
|
T | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8665T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857962 | ||||||
chr6:136858005
|
A | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-8622A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858005 | ||||||
chr6:136858118
|
T | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.527-8509T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858118 | ||||||
chr6:136858249
|
G | A | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8378G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858249 | ||||||
chr6:136858311
|
C | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8316C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858311 | ||||||
chr6:136858340
|
T | C | 2 | a0001c0001t0002g0196a0001c0001t0002g0203 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.527-8287T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858340 | ||||||
chr6:136858471
|
A | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-8156A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858471 | ||||||
chr6:136859277
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.527-7350G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859277 | ||||||
chr6:136859517
|
G | C | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.527-7110G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859517 | ||||||
chr6:136859552
|
G | C | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.527-7075G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859552 | ||||||
chr6:136859617
|
T | C | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-7010T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859617 | ||||||
chr6:136859938
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.527-6689C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859938 | ||||||
chr6:136859948
|
C | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.527-6679C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859948 | ||||||
chr6:136859976
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.527-6651A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859976 | ||||||
chr6:136860014
|
G | GA | 11 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(8): Show | 11 | HG02027.hp1 HG02129.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-6600dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860014 | |||||
chr6:136860200
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.527-6427T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860200 | ||||||
chr6:136860276
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0008g0128 | 3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.527-6351C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860276 | ||||||
chr6:136860285
|
A | G | 1 | a0001c0001t0002g0283 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.527-6342A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860285 | ||||||
chr6:136860409
|
C | CT | 81 | a0001c0001t0001g0008a0001c0001t0001g0084a0001c0001t0001g0086others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.527-6197dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | |||||
chr6:136860409
|
C | CTT | 7 | a0001c0001t0002g0281a0001c0001t0004g0148a0001c0001t0004g0149others(4): Show | 7 | HG00639.hp2 HG01255.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-6198_527-6197d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | |||||
chr6:136860409
|
C | CTTT | 13 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0114others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.527-6199_527-6197d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | |||||
chr6:136860409
|
CT | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0055others(10): Show | 13 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-6197delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | |||||
chr6:136860586
|
G | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-6041G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860586 | ||||||
chr6:136860668
|
T | TA | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-5948dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860668 | |||||
chr6:136860677
|
AAAG | A | 162 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(159): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.527-5947_527-5945d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860677 | |||||
chr6:136860678
|
AAG | A | 22 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(19): Show | 22 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.527-5947_527-5946d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860678 | |||||
chr6:136860724
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0002g0130 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.527-5903T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860724 | ||||||
chr6:136860782
|
A | C | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.527-5845A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860782 | ||||||
chr6:136860891
|
C | T | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-5736C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860891 | ||||||
chr6:136860905
|
C | T | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-5722C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860905 | ||||||
chr6:136860982
|
C | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0248a0001c0001t0002g0277others(1): Show | 5 | HG02056.hp2 NA18612.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-5645C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860982 | ||||||
chr6:136861108
|
A | C | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0139others(5): Show | 8 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-5519A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861108 | ||||||
chr6:136861142
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 8 | HG01891.hp2 HG02015.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-5485C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861142 | ||||||
chr6:136861143
|
G | A | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-5484G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861143 | ||||||
chr6:136861153
|
T | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-5474T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861153 | ||||||
chr6:136861310
|
T | G | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | NA18992.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.527-5317T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861310 | ||||||
chr6:136861437
|
A | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0123 | 3 | HG02257.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.527-5190A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861437 | ||||||
chr6:136861457
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.527-5170A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861457 | ||||||
chr6:136861468
|
A | G | 1 | a0001c0001t0002g0192 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.527-5159A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861468 | ||||||
chr6:136861630
|
G | A | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-4997G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861630 | ||||||
chr6:136861661
|
C | T | 3 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0203 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.527-4966C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861661 | ||||||
chr6:136861837
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.527-4790A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861837 | ||||||
chr6:136862018
|
T | TTTATATA others(32): Show |
1 | a0001c0001t0002g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.527-4595_527-4557d others(41): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862018 | |||||
chr6:136862019
|
T | TTATATAT others(123): Show |
1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.527-4568_527-4567i others(132): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862019 | |||||
chr6:136862019
|
T | TTATATAT others(95): Show |
1 | a0001c0001t0001g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.527-4568_527-4567i others(104): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862019 | |||||
chr6:136862031
|
A | ATATT | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0139others(5): Show | 8 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-4595_527-4594i others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862031 | |||||
chr6:136862034
|
T | A | 8 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0139others(5): Show | 8 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-4593T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862034 | ||||||
chr6:136862034
|
TTATATAT others(8): Show |
T | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-4571_527-4557d others(17): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862034 | |||||
chr6:136862081
|
T | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-4546T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862081 | ||||||
chr6:136862133
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.527-4494C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862133 | ||||||
chr6:136862198
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.527-4429C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862198 | ||||||
chr6:136862266
|
CA | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.527-4360delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862266 | ||||||
chr6:136862469
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-4158G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862469 | ||||||
chr6:136862511
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.527-4116G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862511 | ||||||
chr6:136862801
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.527-3826T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862801 | ||||||
chr6:136862847
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.527-3780G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862847 | ||||||
chr6:136862935
|
G | A | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-3692G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862935 | ||||||
chr6:136863070
|
G | C | 1 | a0001c0001t0002g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.527-3557G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863070 | ||||||
chr6:136863313
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.527-3314A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863313 | ||||||
chr6:136863352
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.527-3275T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863352 | ||||||
chr6:136863354
|
G | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.527-3273G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863354 | ||||||
chr6:136863462
|
G | A | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-3165G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863462 | ||||||
chr6:136863488
|
T | C | 12 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-3139T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863488 | ||||||
chr6:136863522
|
T | C | 192 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.527-3105T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863522 | ||||||
chr6:136863678
|
C | G | 2 | a0001c0001t0002g0194a0001c0001t0004g0151 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.527-2949C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863678 | ||||||
chr6:136863781
|
C | T | 3 | a0001c0001t0002g0230a0001c0001t0002g0233a0001c0001t0002g0283 | 3 | HG02132.hp2 NA18946.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.527-2846C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863781 | ||||||
chr6:136863792
|
G | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-2835G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863792 | ||||||
chr6:136863805
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.527-2822A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863805 | ||||||
chr6:136863877
|
C | G | 20 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0084others(17): Show | 23 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-2750C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863877 | ||||||
chr6:136864004
|
A | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-2623A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864004 | ||||||
chr6:136864026
|
G | A | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-2601G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864026 | ||||||
chr6:136864155
|
A | G | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.527-2472A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864155 | ||||||
chr6:136864178
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0102 | 3 | HG02027.hp2 NA19011.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.527-2449G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864178 | ||||||
chr6:136864216
|
A | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-2411A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864216 | ||||||
chr6:136864240
|
C | CAAT | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-2385_527-2384i others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136864240 | |||||
chr6:136864315
|
TA | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(66): Show | 70 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.527-2302delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136864315 | |||||
chr6:136864315
|
TAA | T | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.527-2303_527-2302d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136864315 | |||||
chr6:136864604
|
A | G | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-2023A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864604 | ||||||
chr6:136864671
|
A | G | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-1956A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864671 | ||||||
chr6:136864697
|
A | T | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-1930A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864697 | ||||||
chr6:136864853
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG01074.hp2 HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.527-1774C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864853 | ||||||
chr6:136864956
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.527-1671T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864956 | ||||||
chr6:136865251
|
G | C | 1 | a0001c0001t0006g0311 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.527-1376G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865251 | ||||||
chr6:136865299
|
T | C | 1 | a0001c0001t0004g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.527-1328T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865299 | ||||||
chr6:136865448
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.527-1179G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865448 | ||||||
chr6:136865521
|
A | G | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0002c0002t0004g0150 | 3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.527-1106A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865521 | ||||||
chr6:136865592
|
C | G | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.527-1035C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865592 | ||||||
chr6:136865614
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.527-1013C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865614 | ||||||
chr6:136865757
|
A | G | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-870A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865757 | ||||||
chr6:136865777
|
C | A | 1 | a0001c0001t0002g0220 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.527-850C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865777 | ||||||
chr6:136865794
|
A | G | 6 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(3): Show | 6 | HG01255.hp2 HG01981.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-833A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865794 | ||||||
chr6:136865807
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527-820G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865807 | ||||||
chr6:136865811
|
G | A | 11 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(8): Show | 14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.527-816G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865811 | ||||||
chr6:136865953
|
T | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-674T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865953 | ||||||
chr6:136866000
|
C | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-627C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866000 | ||||||
chr6:136866082
|
G | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0186 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.527-545G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866082 | ||||||
chr6:136866096
|
A | C | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0002c0002t0004g0150 | 3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.527-531A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866096 | ||||||
chr6:136866120
|
A | T | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.527-507A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866120 | ||||||
chr6:136866121
|
T | G | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-506T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866121 | ||||||
chr6:136866438
|
G | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-189G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866438 | ||||||
chr6:136866468
|
T | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.527-159T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866468 | ||||||
chr6:136866503
|
G | A | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-124G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866503 | ||||||
chr6:136866530
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.527-97G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866530 | ||||||
chr6:136866822
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0088a0001c0001t0001g0098 | 3 | HG03834.hp2 NA18955.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.633+89G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136866822 | ||||||
chr6:136867272
|
T | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+539T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867272 | ||||||
chr6:136867285
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.633+552C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867285 | ||||||
chr6:136867288
|
T | C | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+555T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867288 | ||||||
chr6:136867340
|
G | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0165 | 3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.633+607G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867340 | ||||||
chr6:136867422
|
A | G | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.633+689A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867422 | ||||||
chr6:136867458
|
A | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.633+725A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867458 | ||||||
chr6:136867471
|
C | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.633+738C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867471 | ||||||
chr6:136867597
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.633+864G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867597 | ||||||
chr6:136867650
|
C | T | 10 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0130others(7): Show | 10 | HG02027.hp1 HG02886.hp1 HG03490.hp1 others(7): Show |
intron_variant | MODIFIER | c.633+917C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867650 | ||||||
chr6:136867675
|
G | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.633+942G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867675 | ||||||
chr6:136867777
|
AAAC | A | 165 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(162): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.633+1065_633+1067d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 136867777 | |||||
chr6:136867798
|
C | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0002g0186 | 3 | HG03098.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.633+1065C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867798 | ||||||
chr6:136867798
|
C | CAAA | 17 | a0001c0001t0001g0084a0001c0001t0001g0129a0001c0001t0001g0134others(14): Show | 20 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.633+1069_633+1071d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 136867798 | |||||
chr6:136867909
|
G | T | 1 | a0001c0001t0002g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.633+1176G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867909 | ||||||
chr6:136867969
|
CCA | C | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0114others(12): Show | 15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.633+1237_633+1238d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867969 | ||||||
chr6:136867977
|
G | A | 1 | a0001c0001t0006g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.633+1244G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867977 | ||||||
chr6:136868085
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.633+1352C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868085 | ||||||
chr6:136868173
|
C | G | 29 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(26): Show | 30 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.633+1440C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868173 | ||||||
chr6:136868420
|
T | C | 3 | a0001c0001t0002g0268a0001c0001t0002g0271a0001c0001t0002g0274 | 3 | HG02040.hp2 NA18998.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.634-1470T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868420 | ||||||
chr6:136868442
|
T | C | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.634-1448T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868442 | ||||||
chr6:136868841
|
G | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.634-1049G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868841 | ||||||
chr6:136868911
|
G | C | 17 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0145others(14): Show | 17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.634-979G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868911 | ||||||
chr6:136869070
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.634-820C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869070 | ||||||
chr6:136869272
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.634-618C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869272 | ||||||
chr6:136869703
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.634-187A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869703 | ||||||
chr6:136869738
|
C | T | 17 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0145others(14): Show | 17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.634-152C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869738 | ||||||
chr6:136869771
|
T | C | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.634-119T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869771 | ||||||
chr6:136869816
|
T | C | 1 | a0001c0001t0003g0004 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.634-74T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869816 | ||||||
chr6:136870262
|
A | T | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.747+259A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870262 | ||||||
chr6:136870616
|
T | C | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+613T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870616 | ||||||
chr6:136870687
|
C | G | 23 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(20): Show | 24 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.747+684C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870687 | ||||||
chr6:136870832
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 28 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.747+829G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870832 | ||||||
chr6:136871027
|
A | G | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.747+1024A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871027 | ||||||
chr6:136871312
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.748-886T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871312 | ||||||
chr6:136871390
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.748-808G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871390 | ||||||
chr6:136871684
|
C | G | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.748-514C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871684 | ||||||
chr6:136871992
|
A | AAT | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.748-203_748-202dup others(2): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 136871992 | |||||
chr6:136872298
|
A | G | 25 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0145others(22): Show | 25 | HG00639.hp2 HG01255.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+45A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872298 | ||||||
chr6:136872358
|
A | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0035a0001c0001t0001g0055others(8): Show | 11 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+105A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872358 | ||||||
chr6:136872416
|
C | T | 17 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0145others(14): Show | 17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+163C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872416 | ||||||
chr6:136872616
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+363G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872616 | ||||||
chr6:136872754
|
T | G | 2 | a0001c0001t0002g0216a0001c0001t0002g0249 | 2 | HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.803+501T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872754 | ||||||
chr6:136872895
|
T | C | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+642T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872895 | ||||||
chr6:136872950
|
T | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+697T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872950 | ||||||
chr6:136873001
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+748C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873001 | ||||||
chr6:136873232
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.803+979T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873232 | ||||||
chr6:136873388
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.803+1135T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873388 | ||||||
chr6:136873584
|
G | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+1331G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873584 | ||||||
chr6:136873629
|
C | G | 1 | a0001c0001t0002g0313 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.803+1376C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873629 | ||||||
chr6:136873696
|
G | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0008g0128 | 3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+1443G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873696 | ||||||
chr6:136873719
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.803+1466T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873719 | ||||||
chr6:136873859
|
C | G | 1 | a0001c0001t0002g0299 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.803+1606C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873859 | ||||||
chr6:136874044
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(24): Show | 28 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.803+1791G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874044 | ||||||
chr6:136874076
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.803+1823T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874076 | ||||||
chr6:136874138
|
G | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+1885G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874138 | ||||||
chr6:136874236
|
G | C | 2 | a0001c0001t0002g0137a0001c0001t0002g0186 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.803+1983G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874236 | ||||||
chr6:136874320
|
C | T | 167 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0158others(164): Show | 170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.803+2067C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874320 | ||||||
chr6:136874400
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.803+2147A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874400 | ||||||
chr6:136874438
|
A | C | 1 | a0001c0001t0002g0201 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.803+2185A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874438 | ||||||
chr6:136874530
|
C | G | 166 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0189others(163): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.803+2277C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874530 | ||||||
chr6:136874656
|
G | A | 1 | a0001c0001t0008g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.803+2403G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874656 | ||||||
chr6:136874668
|
C | CA | 15 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0050others(12): Show | 15 | HG00423.hp1 HG00438.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.803+2435dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136874668 | |||||
chr6:136874668
|
CA | C | 8 | a0001c0001t0001g0064a0001c0001t0001g0178a0001c0001t0001g0189others(5): Show | 8 | HG00609.hp2 HG00639.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+2435delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136874668 | |||||
chr6:136874693
|
A | C | 1 | a0001c0001t0002g0283 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.803+2440A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874693 | ||||||
chr6:136874807
|
T | C | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+2554T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874807 | ||||||
chr6:136874846
|
A | T | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+2593A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874846 | ||||||
chr6:136875006
|
G | T | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0114others(12): Show | 15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+2753G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875006 | ||||||
chr6:136875094
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0067 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.803+2841G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875094 | ||||||
chr6:136875159
|
C | CT | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+2917dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136875159 | |||||
chr6:136875230
|
T | C | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+2977T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875230 | ||||||
chr6:136875277
|
T | TTAA | 166 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0189others(163): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.803+3025_803+3027d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136875277 | |||||
chr6:136875362
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.803+3109A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875362 | ||||||
chr6:136875511
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.803+3258T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875511 | ||||||
chr6:136875557
|
G | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+3304G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875557 | ||||||
chr6:136875786
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803+3533A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875786 | ||||||
chr6:136875850
|
G | C | 1 | a0001c0001t0005g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.803+3597G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875850 | ||||||
chr6:136875888
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.803+3635A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875888 | ||||||
chr6:136875957
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.803+3704C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875957 | ||||||
chr6:136876042
|
AT | A | 185 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(182): Show | 192 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.803+3802delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136876042 | |||||
chr6:136876261
|
TCTC | T | 13 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0003g0004others(10): Show | 16 | HG02257.hp2 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.803+4011_803+4013d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136876261 | |||||
chr6:136876272
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.803+4019C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876272 | ||||||
chr6:136876583
|
C | T | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.803+4330C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876583 | ||||||
chr6:136876605
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.803+4352C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876605 | ||||||
chr6:136876667
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.803+4414C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876667 | ||||||
chr6:136876729
|
A | G | 12 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0116others(9): Show | 12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+4476A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876729 | ||||||
chr6:136876875
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+4622A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876875 | ||||||
chr6:136877075
|
T | A | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(9): Show | 12 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+4822T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877075 | ||||||
chr6:136877150
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803+4897A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877150 | ||||||
chr6:136877461
|
T | C | 1 | a0001c0001t0002g0288 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.803+5208T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877461 | ||||||
chr6:136877912
|
G | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+5659G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877912 | ||||||
chr6:136878212
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803+5959G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878212 | ||||||
chr6:136878217
|
G | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+5964G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878217 | ||||||
chr6:136878257
|
C | T | 1 | a0001c0001t0002g0268 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.803+6004C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878257 | ||||||
chr6:136878397
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+6144A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878397 | ||||||
chr6:136878413
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.803+6160C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878413 | ||||||
chr6:136878589
|
A | T | 5 | a0001c0001t0002g0188a0001c0001t0002g0198a0001c0001t0002g0200others(2): Show | 5 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+6336A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878589 | ||||||
chr6:136878642
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6389A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878642 | ||||||
chr6:136878683
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.803+6430A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878683 | ||||||
chr6:136878704
|
C | T | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0114others(12): Show | 15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+6451C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878704 | ||||||
chr6:136878878
|
C | CTT | 158 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0189others(155): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.803+6625_803+6626i others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878878 | ||||||
chr6:136879028
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803+6775C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879028 | ||||||
chr6:136879052
|
G | T | 1 | a0001c0001t0001g0064 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6799G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879052 | ||||||
chr6:136879081
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6828C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879081 | ||||||
chr6:136879084
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6831T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879084 | ||||||
chr6:136879088
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6835C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879088 | ||||||
chr6:136879167
|
A | T | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0004g0114others(12): Show | 15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+6914A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879167 | ||||||
chr6:136879289
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803+7036T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879289 | ||||||
chr6:136879598
|
T | G | 1 | a0001c0001t0004g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803+7345T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879598 | ||||||
chr6:136879685
|
A | C | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+7432A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879685 | ||||||
chr6:136879707
|
A | C | 2 | a0001c0001t0002g0210a0001c0001t0002g0227 | 2 | HG01169.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.803+7454A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879707 | ||||||
chr6:136879882
|
A | C | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+7629A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879882 | ||||||
chr6:136880126
|
T | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+7873T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880126 | ||||||
chr6:136880140
|
G | C | 1 | a0001c0001t0002g0282 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803+7887G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880140 | ||||||
chr6:136880287
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.803+8034A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880287 | ||||||
chr6:136880791
|
T | A | 1 | a0001c0001t0002g0251 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.803+8538T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880791 | ||||||
chr6:136880861
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+8608G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880861 | ||||||
chr6:136880971
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.803+8718A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880971 | ||||||
chr6:136880974
|
A | G | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0002c0002t0004g0150 | 3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.803+8721A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880974 | ||||||
chr6:136881140
|
T | C | 2 | a0001c0001t0002g0142a0001c0001t0002g0143 | 2 | NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.803+8887T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136881140 | ||||||
chr6:136881367
|
C | T | 11 | a0001c0001t0001g0189a0001c0001t0002g0130a0001c0001t0002g0183others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.803+9114C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136881367 | ||||||
chr6:136881965
|
C | G | 11 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(8): Show | 14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.803+9712C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136881965 | ||||||
chr6:136882058
|
A | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+9805A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882058 | ||||||
chr6:136882078
|
T | C | 2 | a0001c0001t0003g0005a0001c0001t0003g0120 | 3 | HG02647.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.803+9825T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882078 | ||||||
chr6:136882093
|
A | G | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | NA18955.hp1 NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.803+9840A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882093 | ||||||
chr6:136882175
|
C | CT | 61 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(58): Show | 66 | HG00323.hp2 HG00558.hp2 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.803+9944dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882175 | |||||
chr6:136882175
|
C | CTT | 7 | a0001c0001t0001g0045a0001c0001t0001g0136a0001c0001t0001g0176others(4): Show | 7 | HG00423.hp2 HG00597.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+9943_803+9944d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882175 | |||||
chr6:136882175
|
CT | C | 24 | a0001c0001t0001g0030a0001c0001t0001g0050a0001c0001t0001g0085others(21): Show | 24 | HG01255.hp2 HG01981.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.803+9944delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882175 | |||||
chr6:136882177
|
T | TC | 3 | a0001c0001t0001g0084a0001c0001t0002g0183a0001c0001t0002g0317 | 3 | HG02630.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.803+9924_803+9925i others(3): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882177 | ||||||
chr6:136882178
|
T | C | 10 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0081others(7): Show | 10 | HG01358.hp1 HG01981.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.803+9925T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882178 | ||||||
chr6:136882346
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.803+10093C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882346 | ||||||
chr6:136882548
|
A | AAAT | 140 | a0001c0001t0001g0189a0001c0001t0002g0009a0001c0001t0002g0010others(137): Show | 143 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.803+10314_803+1031 others(7): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882548 | |||||
chr6:136882608
|
G | A | 185 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.803+10355G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882608 | ||||||
chr6:136882692
|
G | A | 1 | a0001c0001t0002g0259 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.803+10439G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882692 | ||||||
chr6:136882719
|
C | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0217 | 2 | HG02056.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.803+10466C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882719 | ||||||
chr6:136882769
|
A | G | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+10516A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882769 | ||||||
chr6:136882877
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803+10624C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882877 | ||||||
chr6:136882878
|
G | C | 169 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0189others(166): Show | 172 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.803+10625G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882878 | ||||||
chr6:136882880
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+10627A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882880 | ||||||
chr6:136882928
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.803+10675G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882928 | ||||||
chr6:136883038
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.803+10785G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883038 | ||||||
chr6:136883142
|
C | T | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+10889C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883142 | ||||||
chr6:136883184
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.803+10931C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883184 | ||||||
chr6:136883420
|
T | G | 11 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(8): Show | 11 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+11167T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883420 | ||||||
chr6:136883453
|
C | T | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.803+11200C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883453 | ||||||
chr6:136883497
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.803+11244A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883497 | ||||||
chr6:136883501
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.803+11248T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883501 | ||||||
chr6:136883597
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.803+11344C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883597 | ||||||
chr6:136883692
|
C | T | 17 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0145others(14): Show | 17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+11439C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883692 | ||||||
chr6:136883740
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+11487G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883740 | ||||||
chr6:136883741
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+11488G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883741 | ||||||
chr6:136883960
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.803+11707G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883960 | ||||||
chr6:136884042
|
C | T | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | NA18955.hp1 NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.803+11789C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884042 | ||||||
chr6:136884070
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+11817A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884070 | ||||||
chr6:136884230
|
G | A | 17 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0145others(14): Show | 17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+11977G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884230 | ||||||
chr6:136884357
|
C | G | 2 | a0001c0001t0002g0250a0001c0001t0002g0301 | 2 | NA19007.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.803+12104C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884357 | ||||||
chr6:136884505
|
A | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.803+12252A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884505 | ||||||
chr6:136884513
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.803+12260A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884513 | ||||||
chr6:136884626
|
TTTGAAA | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+12376_803+1238 others(10): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136884626 | |||||
chr6:136884635
|
C | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+12382C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884635 | ||||||
chr6:136884834
|
T | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+12581T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884834 | ||||||
chr6:136884943
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0285 | 2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.803+12690C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884943 | ||||||
chr6:136884944
|
G | A | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0002c0002t0004g0150 | 3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.803+12691G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884944 | ||||||
chr6:136885124
|
A | G | 193 | a0001c0001t0001g0008a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+12871A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885124 | ||||||
chr6:136885187
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+12934A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885187 | ||||||
chr6:136885436
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0317 | 3 | HG02109.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.804-12706G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885436 | ||||||
chr6:136885790
|
A | G | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.804-12352A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885790 | ||||||
chr6:136885793
|
G | C | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.804-12349G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885793 | ||||||
chr6:136886166
|
G | A | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.804-11976G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886166 | ||||||
chr6:136886293
|
A | T | 1 | a0001c0001t0006g0316 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.804-11849A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886293 | ||||||
chr6:136886435
|
A | G | 1 | a0001c0001t0008g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804-11707A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886435 | ||||||
chr6:136886551
|
G | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0186 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.804-11591G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886551 | ||||||
chr6:136886735
|
ATGTC | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.804-11404_804-1140 others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136886735 | |||||
chr6:136887489
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.804-10653A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136887489 | ||||||
chr6:136887600
|
A | G | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-10542A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136887600 | ||||||
chr6:136887625
|
TAAAAC | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(21): Show | 25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.804-10513_804-1050 others(9): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136887625 | |||||
chr6:136887854
|
T | G | 1 | a0001c0001t0001g0172 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.804-10288T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136887854 | ||||||
chr6:136888141
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.804-10001C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888141 | ||||||
chr6:136888173
|
G | C | 164 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(161): Show | 167 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.804-9969G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888173 | ||||||
chr6:136888453
|
A | G | 50 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0048others(47): Show | 52 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.804-9689A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888453 | ||||||
chr6:136888570
|
G | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-9572G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888570 | ||||||
chr6:136888579
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.804-9563A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888579 | ||||||
chr6:136888695
|
A | G | 1 | a0001c0001t0002g0258 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.804-9447A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888695 | ||||||
chr6:136888720
|
A | T | 15 | a0001c0001t0002g0010a0001c0001t0002g0207a0001c0001t0002g0208others(12): Show | 16 | HG02074.hp1 NA18944.hp1 NA18949.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-9422A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888720 | ||||||
chr6:136888795
|
T | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-9347T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888795 | ||||||
chr6:136888804
|
G | A | 3 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0203 | 3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.804-9338G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888804 | ||||||
chr6:136888903
|
T | C | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(18): Show | 21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-9239T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888903 | ||||||
chr6:136889391
|
C | T | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.804-8751C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889391 | ||||||
chr6:136889431
|
A | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-8711A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889431 | ||||||
chr6:136889563
|
T | C | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0008g0128 | 3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.804-8579T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889563 | ||||||
chr6:136889574
|
A | T | 18 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(15): Show | 18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.804-8568A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889574 | ||||||
chr6:136889806
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.804-8336A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889806 | ||||||
chr6:136889948
|
C | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0026others(4): Show | 9 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-8194C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889948 | ||||||
chr6:136890183
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.804-7959C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890183 | ||||||
chr6:136890257
|
A | C | 8 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-7885A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890257 | ||||||
chr6:136890350
|
C | G | 23 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0160others(20): Show | 24 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.804-7792C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890350 | ||||||
chr6:136890391
|
A | G | 4 | a0001c0001t0002g0271a0001c0001t0007g0012a0001c0001t0007g0013others(1): Show | 4 | HG03139.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.804-7751A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890391 | ||||||
chr6:136890416
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 7 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-7726C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890416 | ||||||
chr6:136890435
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.804-7707C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890435 | ||||||
chr6:136890514
|
G | T | 135 | a0001c0001t0001g0189a0001c0001t0002g0009a0001c0001t0002g0010others(132): Show | 138 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.804-7628G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890514 | ||||||
chr6:136890785
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.804-7357C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890785 | ||||||
chr6:136891038
|
G | C | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-7104G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891038 | ||||||
chr6:136891235
|
G | A | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.804-6907G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891235 | ||||||
chr6:136891279
|
A | G | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.804-6863A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891279 | ||||||
chr6:136891395
|
T | C | 13 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0003g0004others(10): Show | 16 | HG02257.hp2 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.804-6747T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891395 | ||||||
chr6:136891454
|
A | G | 18 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(15): Show | 18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.804-6688A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891454 | ||||||
chr6:136891651
|
CT | C | 19 | a0001c0001t0001g0058a0001c0001t0001g0092a0001c0001t0001g0099others(16): Show | 19 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.804-6476delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136891651 | |||||
chr6:136891782
|
A | C | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.804-6360A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891782 | ||||||
chr6:136891817
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.804-6325G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891817 | ||||||
chr6:136891916
|
G | A | 1 | a0001c0001t0011g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.804-6226G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891916 | ||||||
chr6:136891921
|
C | T | 2 | a0001c0001t0003g0004a0001c0001t0003g0123 | 3 | HG02257.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.804-6221C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891921 | ||||||
chr6:136892009
|
A | G | 3 | a0001c0001t0002g0268a0001c0001t0002g0271a0001c0001t0002g0274 | 3 | HG02040.hp2 NA18998.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.804-6133A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892009 | ||||||
chr6:136892037
|
T | C | 1 | a0001c0001t0002g0230 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.804-6105T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892037 | ||||||
chr6:136892260
|
T | C | 4 | a0001c0001t0002g0298a0001c0001t0006g0310a0001c0001t0006g0311others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.804-5882T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892260 | ||||||
chr6:136892957
|
T | A | 6 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(3): Show | 6 | HG01255.hp2 HG01981.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.804-5185T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892957 | ||||||
chr6:136893009
|
T | C | 191 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(188): Show | 198 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.804-5133T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893009 | ||||||
chr6:136893068
|
C | T | 201 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(198): Show | 208 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.804-5074C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893068 | ||||||
chr6:136893151
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.804-4991G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893151 | ||||||
chr6:136893199
|
T | A | 1 | a0001c0001t0002g0238 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.804-4943T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893199 | ||||||
chr6:136893202
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0008 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.804-4933_804-4932i others(33): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136893202 | |||||
chr6:136893268
|
T | G | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.804-4874T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893268 | ||||||
chr6:136893278
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.804-4864G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893278 | ||||||
chr6:136893320
|
G | T | 1 | a0001c0001t0002g0241 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.804-4822G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893320 | ||||||
chr6:136893444
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804-4698C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893444 | ||||||
chr6:136893466
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0186 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.804-4676C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893466 | ||||||
chr6:136893503
|
T | A | 10 | a0001c0001t0002g0130a0001c0001t0002g0183a0001c0001t0002g0184others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.804-4639T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893503 | ||||||
chr6:136893549
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.804-4593G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893549 | ||||||
chr6:136893688
|
A | G | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(18): Show | 21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-4454A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893688 | ||||||
chr6:136894023
|
G | A | 7 | a0001c0001t0002g0193a0001c0001t0002g0214a0001c0001t0002g0252others(4): Show | 7 | HG02148.hp1 NA18948.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-4119G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894023 | ||||||
chr6:136894186
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.804-3956C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894186 | ||||||
chr6:136894218
|
G | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.804-3924G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894218 | ||||||
chr6:136894241
|
A | G | 201 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(198): Show | 208 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.804-3901A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894241 | ||||||
chr6:136894318
|
A | T | 1 | a0001c0001t0002g0257 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.804-3824A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894318 | ||||||
chr6:136894390
|
G | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-3752G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894390 | ||||||
chr6:136894393
|
C | T | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(18): Show | 21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-3749C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894393 | ||||||
chr6:136894415
|
T | C | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(18): Show | 21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-3727T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894415 | ||||||
chr6:136894501
|
A | G | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(18): Show | 21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-3641A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894501 | ||||||
chr6:136894545
|
G | A | 122 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(119): Show | 125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.804-3597G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894545 | ||||||
chr6:136894739
|
G | A | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-3403G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894739 | ||||||
chr6:136894928
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-3214A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894928 | ||||||
chr6:136895003
|
A | T | 2 | a0001c0001t0004g0152a0001c0001t0008g0015 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.804-3139A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895003 | ||||||
chr6:136895629
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.804-2513C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895629 | ||||||
chr6:136895631
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-2511T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895631 | ||||||
chr6:136895709
|
A | T | 156 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(153): Show | 159 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.804-2433A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895709 | ||||||
chr6:136895778
|
A | G | 1 | a0001c0001t0002g0256 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.804-2364A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895778 | ||||||
chr6:136895803
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.804-2339C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895803 | ||||||
chr6:136895877
|
TG | T | 10 | a0001c0001t0002g0130a0001c0001t0002g0183a0001c0001t0002g0184others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.804-2263delG | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136895877 | |||||
chr6:136896129
|
C | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-2013C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136896129 | ||||||
chr6:136896216
|
A | G | 1 | a0001c0001t0002g0225 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.804-1926A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136896216 | ||||||
chr6:136896604
|
G | GTCCTTCC others(60): Show |
1 | a0001c0001t0002g0309 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.804-1475_804-1474i others(69): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136896604 | |||||
chr6:136896974
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.804-1168T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136896974 | ||||||
chr6:136897124
|
G | A | 15 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(12): Show | 15 | HG00323.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-1018G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897124 | ||||||
chr6:136897507
|
T | G | 1 | a0001c0001t0009g0156 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.804-635T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897507 | ||||||
chr6:136897554
|
T | C | 124 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(121): Show | 127 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.804-588T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897554 | ||||||
chr6:136897632
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.804-510A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897632 | ||||||
chr6:136897696
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.804-446A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897696 | ||||||
chr6:136898096
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.804-46T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136898096 | ||||||
chr6:136898294
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG02155.hp2 NA18612.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+53C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898294 | ||||||
chr6:136898462
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.903+221A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898462 | ||||||
chr6:136898589
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.903+348T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898589 | ||||||
chr6:136898593
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+352C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898593 | ||||||
chr6:136898800
|
T | C | 10 | a0001c0001t0002g0130a0001c0001t0002g0183a0001c0001t0002g0184others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+559T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898800 | ||||||
chr6:136898819
|
T | A | 139 | a0001c0001t0001g0189a0001c0001t0002g0009a0001c0001t0002g0010others(136): Show | 142 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.903+578T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898819 | ||||||
chr6:136898855
|
A | G | 18 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(15): Show | 18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+614A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898855 | ||||||
chr6:136899080
|
C | CT | 13 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0169others(10): Show | 13 | HG01255.hp2 HG01884.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+857dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899080 | |||||
chr6:136899080
|
C | CTT | 119 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(116): Show | 122 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.903+856_903+857dup others(2): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899080 | |||||
chr6:136899080
|
CT | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0050others(4): Show | 9 | NA18949.hp2 NA18960.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+857delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899080 | |||||
chr6:136899084
|
T | TC | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+843_903+844ins others(1): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899084 | ||||||
chr6:136899087
|
T | TC | 3 | a0001c0001t0007g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.903+846_903+847ins others(1): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899087 | ||||||
chr6:136899142
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.903+901G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899142 | ||||||
chr6:136899193
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.903+952A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899193 | ||||||
chr6:136899197
|
C | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0027 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.903+956C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899197 | ||||||
chr6:136899247
|
A | AT | 12 | a0001c0001t0001g0189a0001c0001t0004g0147a0001c0001t0004g0148others(9): Show | 12 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+1020dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899247 | |||||
chr6:136899265
|
A | C | 10 | a0001c0001t0002g0130a0001c0001t0002g0183a0001c0001t0002g0184others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+1024A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899265 | ||||||
chr6:136899269
|
T | C | 2 | a0001c0001t0004g0152a0001c0001t0008g0015 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.903+1028T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899269 | ||||||
chr6:136899275
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.903+1034C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899275 | ||||||
chr6:136899571
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.903+1330G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899571 | ||||||
chr6:136899648
|
G | A | 10 | a0001c0001t0002g0130a0001c0001t0002g0183a0001c0001t0002g0184others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+1407G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899648 | ||||||
chr6:136899927
|
C | G | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.903+1686C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899927 | ||||||
chr6:136899968
|
T | C | 18 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(15): Show | 18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+1727T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899968 | ||||||
chr6:136900104
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.903+1863G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900104 | ||||||
chr6:136900117
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.903+1876G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900117 | ||||||
chr6:136900228
|
A | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.903+1987A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900228 | ||||||
chr6:136900468
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.903+2227C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900468 | ||||||
chr6:136900690
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.903+2449G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900690 | ||||||
chr6:136900821
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.903+2580G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900821 | ||||||
chr6:136900831
|
T | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0248a0001c0001t0002g0277others(1): Show | 5 | HG02056.hp2 NA18612.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+2590T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900831 | ||||||
chr6:136901093
|
T | C | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0008g0128 | 3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.903+2852T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901093 | ||||||
chr6:136901152
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+2911C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901152 | ||||||
chr6:136901249
|
T | A | 32 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(29): Show | 32 | HG00639.hp2 HG01192.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.903+3008T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901249 | ||||||
chr6:136901453
|
G | C | 18 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(15): Show | 18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+3212G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901453 | ||||||
chr6:136901533
|
A | G | 164 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(161): Show | 167 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.903+3292A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901533 | ||||||
chr6:136901832
|
C | T | 1 | a0001c0001t0002g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.903+3591C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901832 | ||||||
chr6:136901846
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.903+3605C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901846 | ||||||
chr6:136901974
|
G | A | 6 | a0001c0001t0004g0147a0001c0001t0004g0148a0001c0001t0004g0149others(3): Show | 6 | HG01255.hp2 HG01981.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+3733G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901974 | ||||||
chr6:136902301
|
G | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0307 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.903+4060G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902301 | ||||||
chr6:136902421
|
T | C | 1 | a0001c0001t0004g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.903+4180T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902421 | ||||||
chr6:136902541
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | NA18992.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.903+4300C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902541 | ||||||
chr6:136902637
|
T | C | 1 | a0001c0001t0002g0265 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.903+4396T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902637 | ||||||
chr6:136902729
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.903+4488A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902729 | ||||||
chr6:136902770
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.903+4529A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902770 | ||||||
chr6:136903032
|
T | C | 2 | a0001c0001t0005g0121a0001c0001t0005g0125 | 2 | HG00639.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.903+4791T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903032 | ||||||
chr6:136903205
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.903+4964A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903205 | ||||||
chr6:136903336
|
C | CT | 123 | a0001c0001t0001g0035a0001c0001t0001g0077a0001c0001t0001g0086others(120): Show | 126 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.903+5114dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136903336 | |||||
chr6:136903724
|
G | C | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(18): Show | 21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.903+5483G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903724 | ||||||
chr6:136903762
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.903+5521C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903762 | ||||||
chr6:136903828
|
A | C | 1 | a0001c0001t0002g0257 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.903+5587A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903828 | ||||||
chr6:136903829
|
CT | C | 43 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0050others(40): Show | 43 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.903+5603delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136903829 | |||||
chr6:136903863
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+5622G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903863 | ||||||
chr6:136903908
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.903+5667G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903908 | ||||||
chr6:136904104
|
TAGA | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+5867_903+5869d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136904104 | |||||
chr6:136904143
|
G | A | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+5902G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904143 | ||||||
chr6:136904373
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.903+6132T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904373 | ||||||
chr6:136904444
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.903+6203T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904444 | ||||||
chr6:136904632
|
C | CT | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(6): Show | 9 | HG00544.hp1 HG00597.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.903+6409dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136904632 | |||||
chr6:136904632
|
CT | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0163a0001c0001t0002g0130others(11): Show | 15 | HG00323.hp2 HG01516.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.903+6409delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136904632 | |||||
chr6:136904670
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(2): Show | 5 | NA18953.hp1 NA18969.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+6429G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904670 | ||||||
chr6:136904678
|
A | T | 1 | a0001c0001t0002g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.903+6437A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904678 | ||||||
chr6:136904705
|
C | T | 18 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(15): Show | 18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+6464C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904705 | ||||||
chr6:136904779
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+6538T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904779 | ||||||
chr6:136904783
|
A | G | 2 | a0001c0001t0002g0137a0001c0001t0002g0186 | 2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.903+6542A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904783 | ||||||
chr6:136904874
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.903+6633C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904874 | ||||||
chr6:136905025
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.903+6784G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905025 | ||||||
chr6:136905133
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.903+6892C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905133 | ||||||
chr6:136905320
|
T | C | 3 | a0001c0001t0004g0148a0001c0001t0004g0149a0002c0002t0004g0150 | 3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.903+7079T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905320 | ||||||
chr6:136905422
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.903+7181C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905422 | ||||||
chr6:136905559
|
C | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+7318C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905559 | ||||||
chr6:136905695
|
A | G | 1 | a0001c0001t0004g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.903+7454A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905695 | ||||||
chr6:136906051
|
C | T | 4 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0118others(1): Show | 6 | HG02572.hp1 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-7407C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906051 | ||||||
chr6:136906137
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.904-7321A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906137 | ||||||
chr6:136906301
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.904-7157T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906301 | ||||||
chr6:136906433
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.904-7025C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906433 | ||||||
chr6:136906534
|
G | T | 9 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(6): Show | 9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-6924G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906534 | ||||||
chr6:136906749
|
C | G | 20 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0084others(17): Show | 23 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.904-6709C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906749 | ||||||
chr6:136906841
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0084 | 3 | HG03130.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.904-6617C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906841 | ||||||
chr6:136906956
|
G | A | 189 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(186): Show | 196 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.904-6502G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906956 | ||||||
chr6:136906962
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.904-6496C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906962 | ||||||
chr6:136907159
|
C | G | 2 | a0001c0001t0001g0300a0001c0001t0001g0306 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.904-6299C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907159 | ||||||
chr6:136907213
|
C | G | 1 | a0001c0001t0002g0257 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.904-6245C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907213 | ||||||
chr6:136907496
|
TC | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(23): Show | 30 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.904-5961delC | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907496 | ||||||
chr6:136907509
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.904-5949A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907509 | ||||||
chr6:136907514
|
T | C | 16 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(13): Show | 16 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.904-5944T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907514 | ||||||
chr6:136908006
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.904-5452G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908006 | ||||||
chr6:136908105
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.904-5353A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908105 | ||||||
chr6:136908219
|
G | A | 1 | a0001c0001t0002g0278 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.904-5239G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908219 | ||||||
chr6:136908262
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.904-5196A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908262 | ||||||
chr6:136908332
|
T | A | 1 | a0001c0001t0002g0283 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.904-5126T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908332 | ||||||
chr6:136908340
|
GT | G | 5 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0110others(2): Show | 5 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-5110delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136908340 | |||||
chr6:136908389
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(310): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.904-5069G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908389 | ||||||
chr6:136908642
|
A | G | 8 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(5): Show | 8 | HG01192.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-4816A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908642 | ||||||
chr6:136908676
|
CAA | C | 11 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(8): Show | 14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.904-4781_904-4780d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908676 | ||||||
chr6:136908721
|
A | G | 1 | a0001c0001t0002g0261 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.904-4737A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908721 | ||||||
chr6:136908764
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(8): Show | 12 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.904-4694A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908764 | ||||||
chr6:136908823
|
G | T | 4 | a0001c0001t0002g0144a0001c0001t0002g0212a0001c0001t0002g0244others(1): Show | 4 | HG03710.hp2 NA18942.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-4635G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908823 | ||||||
chr6:136908830
|
T | TC | 5 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 6 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-4625dupC | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136908830 | |||||
chr6:136908833
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.904-4625C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908833 | ||||||
chr6:136908870
|
CT | C | 3 | a0001c0001t0002g0138a0001c0001t0002g0144a0001c0001t0002g0315 | 3 | HG03490.hp1 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.904-4587delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908870 | ||||||
chr6:136908903
|
G | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0002g0137others(4): Show | 7 | HG02258.hp2 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-4555G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908903 | ||||||
chr6:136908974
|
A | G | 1 | a0001c0001t0004g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.904-4484A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908974 | ||||||
chr6:136909048
|
T | C | 13 | a0001c0001t0001g0136a0001c0001t0003g0004a0001c0001t0003g0005others(10): Show | 16 | HG01255.hp2 HG01981.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.904-4410T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909048 | ||||||
chr6:136909079
|
A | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0084others(13): Show | 16 | HG02145.hp2 HG02572.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.904-4379A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909079 | ||||||
chr6:136909147
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.904-4311A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909147 | ||||||
chr6:136909178
|
A | G | 1 | a0001c0001t0002g0283 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.904-4280A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909178 | ||||||
chr6:136909311
|
A | AAAAC | 7 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-4135_904-4132d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136909311 | |||||
chr6:136909398
|
C | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-4060C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909398 | ||||||
chr6:136909505
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.904-3953G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909505 | ||||||
chr6:136909511
|
A | G | 6 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(3): Show | 6 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-3947A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909511 | ||||||
chr6:136909527
|
A | T | 1 | a0001c0001t0002g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-3931A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909527 | ||||||
chr6:136909605
|
A | G | 6 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0138others(3): Show | 6 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-3853A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909605 | ||||||
chr6:136909633
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.904-3825A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909633 | ||||||
chr6:136909886
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.904-3572C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909886 | ||||||
chr6:136909974
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.904-3484G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909974 | ||||||
chr6:136909975
|
G | A | 11 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(8): Show | 14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.904-3483G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909975 | ||||||
chr6:136910021
|
A | G | 11 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(8): Show | 14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.904-3437A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910021 | ||||||
chr6:136910136
|
C | G | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-3322C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910136 | ||||||
chr6:136910156
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.904-3302T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910156 | ||||||
chr6:136910211
|
A | G | 9 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.904-3247A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910211 | ||||||
chr6:136910269
|
A | T | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.904-3189A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910269 | ||||||
chr6:136910333
|
A | T | 13 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(10): Show | 13 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-3125A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910333 | ||||||
chr6:136910533
|
A | G | 158 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(155): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-2925A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910533 | ||||||
chr6:136910574
|
A | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0106a0001c0001t0001g0295 | 3 | HG01169.hp2 HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.904-2884A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910574 | ||||||
chr6:136910584
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-2874C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910584 | ||||||
chr6:136910785
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-2673C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910785 | ||||||
chr6:136910892
|
C | T | 158 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(155): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-2566C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910892 | ||||||
chr6:136911041
|
AT | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | NA18955.hp1 NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.904-2412delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136911041 | |||||
chr6:136911417
|
T | C | 10 | a0001c0001t0002g0130a0001c0001t0002g0183a0001c0001t0002g0184others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.904-2041T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911417 | ||||||
chr6:136911459
|
G | C | 1 | a0001c0001t0002g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-1999G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911459 | ||||||
chr6:136911596
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.904-1862G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911596 | ||||||
chr6:136911636
|
A | C | 15 | a0001c0001t0002g0023a0001c0001t0002g0140a0001c0001t0002g0142others(12): Show | 15 | HG00544.hp1 HG02040.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.904-1822A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911636 | ||||||
chr6:136911682
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-1776C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911682 | ||||||
chr6:136911716
|
A | AT | 158 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(155): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-1736dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136911716 | |||||
chr6:136911804
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.904-1654T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911804 | ||||||
chr6:136911860
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.904-1598C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911860 | ||||||
chr6:136912219
|
G | A | 1 | a0001c0001t0002g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.904-1239G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912219 | ||||||
chr6:136912340
|
G | A | 190 | a0001c0001t0001g0007a0001c0001t0001g0092a0001c0001t0001g0099others(187): Show | 197 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.904-1118G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912340 | ||||||
chr6:136912750
|
C | T | 13 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0101others(10): Show | 13 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-708C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912750 | ||||||
chr6:136912792
|
A | G | 158 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(155): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-666A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912792 | ||||||
chr6:136912982
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.904-476C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912982 | ||||||
chr6:136913025
|
T | G | 158 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(155): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-433T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913025 | ||||||
chr6:136913135
|
G | A | 2 | a0001c0001t0002g0263a0001c0001t0002g0266 | 2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.904-323G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913135 | ||||||
chr6:136913144
|
A | C | 198 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(195): Show | 205 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.904-314A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913144 | ||||||
chr6:136913274
|
G | A | 2 | a0001c0001t0009g0156a0001c0001t0011g0153 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.904-184G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913274 |