Item | Value |
---|---|
geneid | 5339 |
ensemblid | ENSG00000178209.17 |
hgncid | 9069 |
symbol | PLEC |
name | plectin |
refseq_nuc | NM_201378.4 |
refseq_prot | NP_958780.1 |
ensembl_nuc | ENST00000356346.7 |
ensembl_prot | ENSP00000348702.3 |
mane_status | MANE Plus Clinical |
chr | chr8 |
start | 143915153 |
end | 143973529 |
strand | - |
ver | v1.2 |
region | chr8:143915153-143973529 |
region5000 | chr8:143910153-143978529 |
regionname0 | PLEC_chr8_143915153_143973529 |
regionname5000 | PLEC_chr8_143910153_143978529 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 4533 | 82 | 2 | 22 | 39 | 6 | 11 | 25 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0002 | 0/0 | 4533 | 43 | 2 | 11 | 20 | 4 | 6 | 17 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0003 | 0/0 | 4533 | 14 | 0 | 9 | 1 | 0 | 4 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0004 | 0/0 | 4533 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0005 | 0/0 | 4533 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0006 | 0/0 | 1648 | 9 | 0 | 1 | 6 | 0 | 2 | 6 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0007 | 0/0 | 4533 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0008 | 0/0 | 1648 | 5 | 0 | 1 | 1 | 0 | 3 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0009 | 0/0 | 4533 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0010 | 0/0 | 4533 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0011 | 0/0 | 4533 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0012 | 0/0 | 4533 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0013 | 0/0 | 4533 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0014 | 0/0 | 4533 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0015 | 0/0 | 4533 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0016 | 0/0 | 4533 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0017 | 0/0 | 4533 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0018 | 0/0 | 4533 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0019 | 0/0 | 4533 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0020 | 0/0 | 4533 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0021 | 0/0 | 1648 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0022 | 0/0 | 4533 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0023 | 0/0 | 4533 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0024 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0025 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0026 | 0/0 | 4533 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0027 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0028 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0029 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0030 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0031 | 0/0 | 1648 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0032 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0033 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0034 | 0/0 | 1648 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0035 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0036 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0037 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0038 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0039 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0040 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0041 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0042 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0043 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0044 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0045 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0046 | 0/0 | 4533 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0047 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0048 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0049 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0050 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0051 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0052 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0053 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0054 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0055 | 0/0 | 1648 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0056 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0057 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0058 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0059 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0060 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0061 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0062 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0063 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0064 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0065 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0066 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0067 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0068 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0069 | 0/0 | 1648 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0070 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0071 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0072 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0073 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0074 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0075 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0076 | 0/0 | 1648 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0077 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0078 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0079 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0080 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0081 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0082 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0083 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0084 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0085 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0086 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0087 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0088 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0089 | 0/0 | 1648 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(1643): Show |
chr8 | 143910153 | 143978529 |
a0090 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0091 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0092 | 0/0 | 4533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0093 | 0/0 | 4533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0094 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
a0095 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | MAGPL others(4528): Show |
chr8 | 143910153 | 143978529 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 13599 | 33 | 1 | 4 | 20 | 2 | 5 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0006 | 0/0 | 13599 | 6 | 1 | 5 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0009 | 0/0 | 13599 | 4 | 0 | 1 | 3 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0013 | 0/0 | 13599 | 3 | 0 | 0 | 3 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0024 | 0/0 | 13599 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0028 | 0/1 | 13599 | 2 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0029 | 0/0 | 13599 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0030 | 0/0 | 13599 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0031 | 0/0 | 13599 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0032 | 0/0 | 13599 | 2 | 0 | 1 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0036 | 0/0 | 13599 | 2 | 0 | 1 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0069 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0072 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0080 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0104 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0106 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0112 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0118 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0121 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0122 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0127 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0128 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0131 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0132 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0133 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0136 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0139 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0140 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0141 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0145 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0149 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0166 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0001c0171 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0002 | 0/0 | 13599 | 23 | 1 | 8 | 7 | 3 | 4 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0005 | 0/0 | 13599 | 7 | 0 | 0 | 7 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0019 | 0/0 | 13599 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0037 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0041 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0046 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0047 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0049 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0051 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0053 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0058 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0059 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0060 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0002c0065 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0003c0004 | 0/0 | 13599 | 8 | 0 | 8 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0003c0105 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0003c0110 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0003c0113 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0003c0114 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0003c0115 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0003c0148 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0008 | 0/0 | 13599 | 5 | 5 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0025 | 0/0 | 13599 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0073 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0074 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0086 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0090 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0096 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0175 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0004c0178 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0005c0003 | 0/0 | 13599 | 8 | 7 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0005c0094 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0005c0095 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0005c0098 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0005c0167 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0006c0014 | 0/0 | 13600 | 3 | 0 | 1 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0006c0034 | 0/0 | 13600 | 2 | 0 | 0 | 0 | 0 | 2 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0006c0150 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0006c0151 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0006c0152 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0006c0153 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0007c0016 | 0/0 | 13599 | 3 | 3 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0007c0035 | 0/0 | 13599 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0007c0075 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0008c0011 | 0/0 | 13600 | 3 | 0 | 0 | 0 | 0 | 3 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0008c0055 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0008c0056 | 0/0 | 13600 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0009c0007 | 0/0 | 13599 | 5 | 5 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0010c0022 | 0/0 | 13599 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0010c0083 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0010c0084 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0011c0088 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0011c0089 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0011c0156 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0011c0169 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0012c0015 | 0/0 | 13599 | 3 | 0 | 0 | 3 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0013c0010 | 0/0 | 13599 | 3 | 0 | 3 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0014c0062 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0014c0063 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0014c0064 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0015c0027 | 0/0 | 13599 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0015c0107 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0016c0012 | 0/0 | 13599 | 3 | 3 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0017c0042 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0017c0052 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0018c0018 | 0/0 | 13599 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0019c0017 | 0/0 | 13599 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0020c0026 | 0/0 | 13599 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0021c0081 | 0/0 | 13600 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0021c0085 | 0/0 | 13600 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0022c0021 | 0/0 | 13599 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0023c0123 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0023c0135 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0024c0023 | 0/0 | 13599 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0025c0020 | 0/0 | 13599 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0026c0033 | 0/0 | 13599 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0027c0124 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0028c0050 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0029c0077 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0030c0129 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0031c0172 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0032c0108 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0033c0066 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0034c0101 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0035c0119 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0036c0057 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0037c0079 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0038c0144 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0039c0111 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0040c0061 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0041c0048 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0042c0164 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0043c0091 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0044c0173 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0045c0109 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0046c0039 | 0/0 | 13599 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0047c0143 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0048c0092 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0049c0120 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0050c0170 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0051c0117 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0052c0174 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0053c0067 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0054c0176 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0055c0068 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0056c0071 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0057c0082 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0058c0163 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0059c0103 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0060c0159 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0061c0161 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0062c0040 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0063c0146 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0064c0087 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0065c0070 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0066c0177 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0067c0157 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0068c0138 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0069c0097 | 0/0 | 13600 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0070c0093 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0071c0160 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0072c0158 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0073c0162 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0074c0043 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0075c0137 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0076c0038 | 0/0 | 13600 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0077c0142 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0078c0100 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0079c0168 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0080c0147 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0081c0126 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0082c0134 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0083c0130 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0084c0102 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0085c0045 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0086c0116 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0087c0125 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0088c0099 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0089c0155 | 0/0 | 13600 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13595): Show |
chr8 | 143910153 | 143978529 | ||
a0090c0076 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0091c0154 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0092c0044 | 0/0 | 13599 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0093c0078 | 0/0 | 13599 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0094c0165 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 | ||
a0095c0054 | 0/0 | 13599 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | ATGGC others(13594): Show |
chr8 | 143910153 | 143978529 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 14683 | 32 | 1 | 3 | 20 | 2 | 5 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0001t0010 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0006t0001 | 0/0 | 14683 | 6 | 1 | 5 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0009t0001 | 0/0 | 14683 | 4 | 0 | 1 | 3 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0013t0001 | 0/0 | 14683 | 3 | 0 | 0 | 3 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0024t0001 | 0/0 | 14683 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0028t0001 | 0/1 | 14683 | 2 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0029t0001 | 0/0 | 14683 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0030t0001 | 0/0 | 14683 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0031t0001 | 0/0 | 14683 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0032t0001 | 0/0 | 14683 | 2 | 0 | 1 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0036t0001 | 0/0 | 14683 | 2 | 0 | 1 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0069t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0072t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0080t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0104t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0106t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0112t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0118t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0121t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0122t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0127t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0128t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0131t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0132t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0133t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0136t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0139t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0140t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0141t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0145t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0149t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0166t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0001c0171t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0002t0002 | 0/0 | 14683 | 22 | 1 | 8 | 7 | 3 | 3 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0002t0013 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0005t0002 | 0/0 | 14683 | 7 | 0 | 0 | 7 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0019t0007 | 0/0 | 14683 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0037t0002 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0041t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0046t0007 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0047t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0049t0002 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0051t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0053t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0058t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0059t0002 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0060t0007 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0002c0065t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0003c0004t0001 | 0/0 | 14683 | 8 | 0 | 8 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0003c0105t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0003c0110t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0003c0113t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0003c0114t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0003c0115t0002 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0003c0148t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0008t0003 | 0/0 | 14683 | 4 | 4 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0008t0012 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0025t0003 | 0/0 | 14683 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0073t0008 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0074t0008 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0086t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0090t0003 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0096t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0175t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0004c0178t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0005c0003t0004 | 0/0 | 14683 | 8 | 7 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0005c0094t0004 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0005c0095t0004 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0005c0098t0004 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0005c0167t0001 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0006c0014t0001 | 0/0 | 14684 | 3 | 0 | 1 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0006c0034t0001 | 0/0 | 14684 | 2 | 0 | 0 | 0 | 0 | 2 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0006c0150t0002 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0006c0151t0009 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0006c0152t0001 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0006c0153t0001 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0007c0016t0006 | 0/0 | 14683 | 3 | 3 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0007c0035t0003 | 0/0 | 14683 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0007c0075t0006 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0008c0011t0002 | 0/0 | 14684 | 3 | 0 | 0 | 0 | 0 | 3 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0008c0055t0002 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0008c0056t0002 | 0/0 | 14684 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0009c0007t0005 | 0/0 | 14682 | 5 | 5 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0010c0022t0005 | 0/0 | 14682 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0010c0083t0005 | 0/0 | 14682 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0010c0084t0005 | 0/0 | 14682 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0011c0088t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0011c0089t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0011c0156t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0011c0169t0001 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0012c0015t0001 | 0/0 | 14683 | 3 | 0 | 0 | 3 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0013c0010t0002 | 0/0 | 14683 | 3 | 0 | 3 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0014c0062t0001 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0014c0063t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0014c0064t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0015c0027t0001 | 0/0 | 14683 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0015c0107t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0016c0012t0004 | 0/0 | 14683 | 3 | 3 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0017c0042t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0017c0052t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0018c0018t0002 | 0/0 | 14683 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0019c0017t0002 | 0/0 | 14683 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0020c0026t0002 | 0/0 | 14683 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0021c0081t0003 | 0/0 | 14684 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0021c0085t0005 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0022c0021t0001 | 0/0 | 14683 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0023c0123t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0023c0135t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0024c0023t0003 | 0/0 | 14683 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0025c0020t0003 | 0/0 | 14683 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0026c0033t0001 | 0/0 | 14683 | 2 | 2 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0027c0124t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0028c0050t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0029c0077t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0030c0129t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0031c0172t0001 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0032c0108t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0033c0066t0002 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0034c0101t0002 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0035c0119t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0036c0057t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0037c0079t0005 | 0/0 | 14682 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0038c0144t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0039c0111t0003 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0040c0061t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0041c0048t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0042c0164t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0043c0091t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0044c0173t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0045c0109t0001 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0046c0039t0002 | 0/0 | 14683 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0047c0143t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0048c0092t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0049c0120t0011 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0050c0170t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0051c0117t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0052c0174t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0053c0067t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0054c0176t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0055c0068t0001 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0056c0071t0005 | 0/0 | 14682 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0057c0082t0005 | 0/0 | 14682 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0058c0163t0006 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0059c0103t0006 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0060c0159t0001 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0061c0161t0006 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0062c0040t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0063c0146t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0064c0087t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0065c0070t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0066c0177t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0067c0157t0005 | 0/0 | 14682 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0068c0138t0005 | 0/0 | 14682 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14677): Show |
chr8 | 143910153 | 143978529 |
a0069c0097t0004 | 0/0 | 14684 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0070c0093t0004 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0071c0160t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0072c0158t0004 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0073c0162t0006 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0074c0043t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0075c0137t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0076c0038t0002 | 0/0 | 14684 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0077c0142t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0078c0100t0002 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0079c0168t0001 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0080c0147t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0081c0126t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0082c0134t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0083c0130t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0084c0102t0002 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0085c0045t0002 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0086c0116t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0087c0125t0001 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0088c0099t0004 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0089c0155t0001 | 0/0 | 14684 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14679): Show |
chr8 | 143910153 | 143978529 |
a0090c0076t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0091c0154t0001 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0092c0044t0002 | 0/0 | 14683 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0093c0078t0003 | 0/0 | 14683 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0094c0165t0001 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
a0095c0054t0002 | 0/0 | 14683 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | AGAGT others(14678): Show |
chr8 | 143910153 | 143978529 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0001t0010g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0006t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0006t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0006t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0006t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0006t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0006t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0009t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0009t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0009t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0009t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0013t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0013t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0024t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0024t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0028t0001g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0028t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0029t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0029t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0030t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0031t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0031t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0032t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0032t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0036t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0036t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0069t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0072t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0080t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0104t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0106t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0112t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0118t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0121t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0122t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0127t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0128t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0131t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0132t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0133t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0136t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0139t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0140t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0141t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0145t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0149t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0166t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0001c0171t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0002t0013g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0005t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0005t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0005t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0005t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0005t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0019t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0019t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0037t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0041t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0046t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0047t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0049t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0051t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0053t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0058t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0059t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0060t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0002c0065t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0004t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0004t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0004t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0004t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0105t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0110t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0113t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0114t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0115t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0003c0148t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0008t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0008t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0008t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0008t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0008t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0025t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0025t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0073t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0074t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0086t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0090t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0096t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0175t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0004c0178t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0003t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0094t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0095t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0098t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0005c0167t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0014t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0014t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0014t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0034t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0034t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0150t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0151t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0152t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0006c0153t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0007c0016t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0007c0016t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0007c0016t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0007c0035t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0007c0035t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0007c0075t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0008c0011t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0008c0011t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0008c0011t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0008c0055t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0008c0056t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0009c0007t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0009c0007t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0009c0007t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0009c0007t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0009c0007t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0010c0022t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0010c0022t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0010c0083t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0010c0084t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0011c0088t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0011c0089t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0011c0156t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0011c0169t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0012c0015t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0012c0015t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0012c0015t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0013c0010t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0013c0010t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0013c0010t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0014c0062t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0014c0063t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0014c0064t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0015c0027t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0015c0027t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0015c0107t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0016c0012t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0016c0012t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0016c0012t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0017c0042t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0017c0052t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0018c0018t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0018c0018t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0019c0017t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0019c0017t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0020c0026t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0020c0026t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0021c0081t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0021c0085t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0022c0021t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0022c0021t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0023c0123t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0023c0135t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0024c0023t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0024c0023t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0025c0020t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0025c0020t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0026c0033t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0026c0033t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0027c0124t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0028c0050t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0029c0077t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0030c0129t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0031c0172t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0032c0108t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0033c0066t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0034c0101t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0035c0119t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0036c0057t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0037c0079t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0038c0144t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0039c0111t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0040c0061t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0041c0048t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0042c0164t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0043c0091t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0044c0173t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0045c0109t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0046c0039t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0047c0143t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0048c0092t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0049c0120t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0050c0170t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0051c0117t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0052c0174t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0053c0067t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0054c0176t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0055c0068t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0056c0071t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0057c0082t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0058c0163t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0059c0103t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0060c0159t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0061c0161t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0062c0040t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0063c0146t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0064c0087t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0065c0070t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0066c0177t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0067c0157t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0068c0138t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0069c0097t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0070c0093t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0071c0160t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0072c0158t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0073c0162t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0074c0043t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0075c0137t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0076c0038t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0077c0142t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0078c0100t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0079c0168t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0080c0147t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0081c0126t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0082c0134t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0083c0130t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0084c0102t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0085c0045t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0086c0116t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0087c0125t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0088c0099t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0089c0155t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0090c0076t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0091c0154t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0092c0044t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0093c0078t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0094c0165t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
a0095c0054t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0027 | c0124 | t0001 | g0186 | EUR | GBR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00099 | hp2 | a0028 | c0050 | t0002 | g0037 | EUR | GBR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00140 | hp2 | a0029 | c0077 | t0001 | g0171 | EUR | GBR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00280 | hp1 | a0001 | c0080 | t0001 | g0189 | EUR | FIN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00280 | hp2 | a0001 | c0036 | t0001 | g0221 | EUR | FIN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00323 | hp1 | a0017 | c0052 | t0002 | g0113 | EUR | FIN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00408 | hp1 | a0001 | c0032 | t0001 | g0066 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00408 | hp2 | a0030 | c0129 | t0001 | g0233 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00423 | hp2 | a0031 | c0172 | t0001 | g0183 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00438 | hp1 | a0012 | c0015 | t0001 | g0182 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00597 | hp1 | a0002 | c0005 | t0002 | g0041 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00597 | hp2 | a0032 | c0108 | t0001 | g0265 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00621 | hp1 | a0001 | c0009 | t0001 | g0197 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00621 | hp2 | a0033 | c0066 | t0002 | g0172 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00639 | hp1 | a0001 | c0036 | t0001 | g0220 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00639 | hp2 | a0003 | c0004 | t0001 | g0297 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00642 | hp1 | a0003 | c0114 | t0001 | g0168 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00673 | hp1 | a0034 | c0101 | t0002 | g0159 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00735 | hp1 | a0013 | c0010 | t0002 | g0043 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00735 | hp2 | a0018 | c0018 | t0002 | g0039 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00741 | hp1 | a0019 | c0017 | t0002 | g0021 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG00741 | hp2 | a0001 | c0112 | t0001 | g0273 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01069 | hp2 | a0035 | c0119 | t0001 | g0190 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01070 | hp1 | a0019 | c0017 | t0002 | g0019 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01070 | hp2 | a0020 | c0026 | t0002 | g0155 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01071 | hp2 | a0020 | c0026 | t0002 | g0156 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01074 | hp1 | a0003 | c0004 | t0001 | g0004 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01074 | hp2 | a0002 | c0065 | t0002 | g0022 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01081 | hp1 | a0001 | c0001 | t0010 | g0148 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01081 | hp2 | a0036 | c0057 | t0002 | g0024 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01106 | hp1 | a0001 | c0141 | t0001 | g0262 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01106 | hp2 | a0002 | c0058 | t0002 | g0023 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01109 | hp1 | a0037 | c0079 | t0005 | g0115 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01109 | hp2 | a0013 | c0010 | t0002 | g0040 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01167 | hp1 | a0038 | c0144 | t0001 | g0270 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0005 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01168 | hp1 | a0003 | c0004 | t0001 | g0225 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01175 | hp1 | a0010 | c0083 | t0005 | g0293 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01192 | hp1 | a0021 | c0081 | t0003 | g0089 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01192 | hp2 | a0006 | c0014 | t0001 | g0200 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01243 | hp1 | a0018 | c0018 | t0002 | g0016 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01256 | hp1 | a0022 | c0021 | t0001 | g0261 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01256 | hp2 | a0001 | c0028 | t0001 | g0267 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01258 | hp1 | a0022 | c0021 | t0001 | g0260 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01258 | hp2 | a0001 | c0166 | t0001 | g0194 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01261 | hp1 | a0001 | c0131 | t0002 | g0163 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01261 | hp2 | a0002 | c0051 | t0002 | g0116 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01346 | hp1 | a0039 | c0111 | t0003 | g0144 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01346 | hp2 | a0040 | c0061 | t0002 | g0109 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01358 | hp1 | a0001 | c0006 | t0001 | g0238 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01358 | hp2 | a0041 | c0048 | t0002 | g0025 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01496 | hp2 | a0008 | c0056 | t0002 | g0046 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01516 | hp1 | a0042 | c0164 | t0001 | g0206 | EUR | IBS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0137 | EUR | IBS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0136 | EUR | IBS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0031 | EUR | IBS | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01884 | hp1 | a0043 | c0091 | t0003 | g0006 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01884 | hp2 | a0044 | c0173 | t0003 | g0213 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01891 | hp1 | a0002 | c0049 | t0002 | g0047 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01891 | hp2 | a0004 | c0074 | t0008 | g0142 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01928 | hp1 | a0001 | c0133 | t0001 | g0170 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01928 | hp2 | a0003 | c0004 | t0001 | g0216 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01934 | hp1 | a0001 | c0032 | t0001 | g0162 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01934 | hp2 | a0001 | c0006 | t0001 | g0278 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01943 | hp1 | a0003 | c0004 | t0001 | g0224 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0111 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01952 | hp1 | a0001 | c0029 | t0001 | g0246 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01952 | hp2 | a0045 | c0109 | t0001 | g0269 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01975 | hp1 | a0004 | c0090 | t0003 | g0153 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01978 | hp1 | a0046 | c0039 | t0002 | g0112 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01978 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01981 | hp2 | a0001 | c0006 | t0001 | g0237 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01993 | hp1 | a0003 | c0004 | t0001 | g0005 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01993 | hp2 | a0001 | c0006 | t0001 | g0277 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02004 | hp1 | a0001 | c0121 | t0001 | g0173 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02004 | hp2 | a0001 | c0029 | t0001 | g0205 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02015 | hp1 | a0023 | c0135 | t0001 | g0232 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02027 | hp1 | a0001 | c0013 | t0001 | g0001 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02027 | hp2 | a0014 | c0064 | t0001 | g0072 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02040 | hp1 | a0047 | c0143 | t0001 | g0184 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02040 | hp2 | a0048 | c0092 | t0001 | g0284 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02055 | hp1 | a0011 | c0156 | t0003 | g0105 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02055 | hp2 | a0049 | c0120 | t0011 | g0256 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02056 | hp2 | a0002 | c0059 | t0002 | g0033 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02074 | hp1 | a0050 | c0170 | t0001 | g0181 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02074 | hp2 | a0023 | c0123 | t0001 | g0161 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02080 | hp2 | a0015 | c0027 | t0001 | g0243 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02083 | hp1 | a0051 | c0117 | t0001 | g0199 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02145 | hp1 | a0053 | c0067 | t0003 | g0091 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02145 | hp2 | a0021 | c0085 | t0005 | g0090 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02155 | hp1 | a0001 | c0013 | t0001 | g0001 | EAS | CDX | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02155 | hp2 | a0002 | c0005 | t0002 | g0055 | EAS | CDX | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02165 | hp1 | a0001 | c0104 | t0001 | g0143 | EAS | CDX | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02165 | hp2 | a0001 | c0145 | t0001 | g0178 | EAS | CDX | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02257 | hp1 | a0009 | c0007 | t0005 | g0076 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02257 | hp2 | a0011 | c0089 | t0003 | g0288 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02258 | hp1 | a0009 | c0007 | t0005 | g0079 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02258 | hp2 | a0054 | c0176 | t0003 | g0139 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02280 | hp1 | a0010 | c0022 | t0005 | g0294 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02280 | hp2 | a0004 | c0096 | t0003 | g0096 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02293 | hp1 | a0001 | c0009 | t0001 | g0236 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02300 | hp1 | a0005 | c0003 | t0004 | g0130 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02300 | hp2 | a0001 | c0171 | t0001 | g0239 | AMR | PEL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02523 | hp1 | a0055 | c0068 | t0001 | g0264 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02523 | hp2 | a0008 | c0055 | t0002 | g0051 | EAS | KHV | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02572 | hp1 | a0058 | c0163 | t0006 | g0104 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02572 | hp2 | a0059 | c0103 | t0006 | g0098 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02622 | hp1 | a0005 | c0003 | t0004 | g0014 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02622 | hp2 | a0025 | c0020 | t0003 | g0093 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02630 | hp1 | a0004 | c0025 | t0003 | g0095 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02630 | hp2 | a0005 | c0003 | t0004 | g0126 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02647 | hp1 | a0004 | c0086 | t0003 | g0217 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02647 | hp2 | a0004 | c0008 | t0003 | g0240 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02683 | hp1 | a0002 | c0002 | t0013 | g0117 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02683 | hp2 | a0001 | c0128 | t0001 | g0234 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02698 | hp1 | a0008 | c0011 | t0002 | g0030 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02698 | hp2 | a0003 | c0148 | t0001 | g0279 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02717 | hp1 | a0060 | c0159 | t0001 | g0118 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02717 | hp2 | a0005 | c0003 | t0004 | g0127 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02723 | hp1 | a0007 | c0035 | t0003 | g0103 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02723 | hp2 | a0061 | c0161 | t0006 | g0102 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02735 | hp2 | a0062 | c0040 | t0002 | g0026 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02738 | hp1 | a0006 | c0034 | t0001 | g0059 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02738 | hp2 | a0063 | c0146 | t0001 | g0271 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02818 | hp1 | a0004 | c0178 | t0003 | g0138 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02818 | hp2 | a0026 | c0033 | t0001 | g0085 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02886 | hp1 | a0005 | c0003 | t0004 | g0122 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02886 | hp2 | a0004 | c0175 | t0003 | g0287 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02895 | hp1 | a0016 | c0012 | t0004 | g0133 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02895 | hp2 | a0004 | c0008 | t0012 | g0082 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02896 | hp1 | a0064 | c0087 | t0003 | g0077 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02896 | hp2 | a0016 | c0012 | t0004 | g0132 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02922 | hp1 | a0025 | c0020 | t0003 | g0092 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02922 | hp2 | a0065 | c0070 | t0003 | g0013 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02965 | hp1 | a0066 | c0177 | t0003 | g0140 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02965 | hp2 | a0005 | c0003 | t0004 | g0123 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02976 | hp1 | a0067 | c0157 | t0005 | g0078 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02976 | hp2 | a0011 | c0169 | t0001 | g0010 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03017 | hp1 | a0001 | c0132 | t0001 | g0215 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03017 | hp2 | a0001 | c0069 | t0001 | g0228 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03041 | hp1 | a0007 | c0016 | t0006 | g0086 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03041 | hp2 | a0005 | c0094 | t0004 | g0134 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03098 | hp1 | a0007 | c0016 | t0006 | g0295 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03098 | hp2 | a0004 | c0008 | t0003 | g0150 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03130 | hp1 | a0009 | c0007 | t0005 | g0080 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03130 | hp2 | a0010 | c0084 | t0005 | g0292 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03195 | hp1 | a0068 | c0138 | t0005 | g0286 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03195 | hp2 | a0014 | c0062 | t0001 | g0106 | AFR | ESN | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03209 | hp1 | a0069 | c0097 | t0004 | g0121 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03209 | hp2 | a0016 | c0012 | t0004 | g0135 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03225 | hp1 | a0070 | c0093 | t0004 | g0129 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03225 | hp2 | a0071 | c0160 | t0003 | g0100 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03239 | hp1 | a0003 | c0110 | t0001 | g0169 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03239 | hp2 | a0001 | c0118 | t0001 | g0151 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03453 | hp1 | a0011 | c0088 | t0003 | g0290 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03453 | hp2 | a0005 | c0003 | t0004 | g0124 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03486 | hp1 | a0005 | c0098 | t0004 | g0125 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03486 | hp2 | a0004 | c0008 | t0003 | g0255 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03492 | hp2 | a0001 | c0127 | t0001 | g0204 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03540 | hp1 | a0073 | c0162 | t0006 | g0101 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03540 | hp2 | a0007 | c0075 | t0006 | g0088 | AFR | GWD | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03579 | hp1 | a0005 | c0003 | t0004 | g0128 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03579 | hp2 | a0010 | c0022 | t0005 | g0011 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03688 | hp1 | a0008 | c0011 | t0002 | g0062 | SAS | STU | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03688 | hp2 | a0003 | c0113 | t0001 | g0147 | SAS | STU | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03704 | hp1 | a0003 | c0105 | t0001 | g0230 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03704 | hp2 | a0074 | c0043 | t0002 | g0044 | SAS | PJL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03834 | hp1 | a0075 | c0137 | t0001 | g0218 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03927 | hp1 | a0008 | c0011 | t0002 | g0029 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03927 | hp2 | a0006 | c0034 | t0001 | g0282 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03942 | hp1 | a0001 | c0149 | t0001 | g0242 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03942 | hp2 | a0076 | c0038 | t0002 | g0074 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG04184 | hp1 | a0002 | c0047 | t0002 | g0018 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | BEB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG04199 | hp1 | a0002 | c0053 | t0002 | g0068 | SAS | STU | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG04199 | hp2 | a0077 | c0142 | t0001 | g0266 | SAS | STU | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0036 | SAS | STU | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0032 | SAS | STU | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18522 | hp1 | a0005 | c0095 | t0004 | g0120 | AFR | YRI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18522 | hp2 | a0079 | c0168 | t0001 | g0012 | AFR | YRI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18747 | hp2 | a0080 | c0147 | t0001 | g0107 | EAS | CHB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18943 | hp2 | a0081 | c0126 | t0001 | g0254 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18944 | hp1 | a0001 | c0136 | t0001 | g0268 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18944 | hp2 | a0014 | c0063 | t0001 | g0110 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18945 | hp1 | a0002 | c0005 | t0002 | g0177 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18945 | hp2 | a0001 | c0122 | t0001 | g0222 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18947 | hp1 | a0015 | c0027 | t0001 | g0165 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18947 | hp2 | a0082 | c0134 | t0001 | g0166 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18952 | hp1 | a0001 | c0030 | t0001 | g0002 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18952 | hp2 | a0002 | c0060 | t0007 | g0048 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18954 | hp1 | a0015 | c0107 | t0001 | g0157 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18954 | hp2 | a0002 | c0005 | t0002 | g0050 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18962 | hp1 | a0001 | c0031 | t0001 | g0179 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18962 | hp2 | a0001 | c0024 | t0001 | g0276 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18971 | hp2 | a0002 | c0005 | t0002 | g0042 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18977 | hp1 | a0002 | c0005 | t0002 | g0069 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18977 | hp2 | a0001 | c0013 | t0001 | g0175 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18979 | hp2 | a0001 | c0031 | t0001 | g0245 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18982 | hp1 | a0006 | c0150 | t0002 | g0231 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18984 | hp1 | a0002 | c0019 | t0007 | g0038 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18994 | hp2 | a0006 | c0014 | t0001 | g0008 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18999 | hp2 | a0012 | c0015 | t0001 | g0198 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19000 | hp1 | a0003 | c0115 | t0002 | g0226 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19007 | hp1 | a0006 | c0152 | t0001 | g0211 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19007 | hp2 | a0002 | c0037 | t0002 | g0065 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19011 | hp1 | a0085 | c0045 | t0002 | g0027 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19011 | hp2 | a0086 | c0116 | t0001 | g0195 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19012 | hp1 | a0001 | c0106 | t0001 | g0244 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19012 | hp2 | a0001 | c0030 | t0001 | g0002 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19030 | hp1 | a0004 | c0073 | t0008 | g0141 | AFR | LWK | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19030 | hp2 | a0087 | c0125 | t0001 | g0119 | AFR | LWK | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19043 | hp1 | a0004 | c0008 | t0003 | g0289 | AFR | LWK | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19043 | hp2 | a0088 | c0099 | t0004 | g0131 | AFR | LWK | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19057 | hp1 | a0002 | c0005 | t0002 | g0056 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19057 | hp2 | a0089 | c0155 | t0001 | g0281 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19067 | hp1 | a0002 | c0046 | t0007 | g0054 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19067 | hp2 | a0001 | c0009 | t0001 | g0252 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19070 | hp1 | a0090 | c0076 | t0001 | g0203 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19070 | hp2 | a0012 | c0015 | t0001 | g0160 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19074 | hp2 | a0001 | c0009 | t0001 | g0296 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19080 | hp1 | a0006 | c0014 | t0001 | g0258 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19080 | hp2 | a0002 | c0019 | t0007 | g0049 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19081 | hp1 | a0001 | c0072 | t0001 | g0248 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19084 | hp2 | a0006 | c0153 | t0001 | g0158 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19088 | hp1 | a0001 | c0024 | t0001 | g0180 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19088 | hp2 | a0091 | c0154 | t0001 | g0280 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19091 | hp1 | a0006 | c0151 | t0009 | g0201 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19091 | hp2 | a0092 | c0044 | t0002 | g0057 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19240 | hp1 | a0009 | c0007 | t0005 | g0081 | AFR | YRI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA19240 | hp2 | a0005 | c0167 | t0001 | g0009 | AFR | YRI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20129 | hp1 | a0024 | c0023 | t0003 | g0212 | AFR | ASW | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20129 | hp2 | a0093 | c0078 | t0003 | g0146 | AFR | ASW | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20752 | hp1 | a0001 | c0139 | t0001 | g0193 | EUR | TSI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20752 | hp2 | a0002 | c0041 | t0002 | g0060 | EUR | TSI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20805 | hp1 | a0001 | c0140 | t0001 | g0285 | EUR | TSI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20805 | hp2 | a0094 | c0165 | t0001 | g0192 | EUR | TSI | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20905 | hp1 | a0017 | c0042 | t0002 | g0176 | SAS | GIH | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20905 | hp2 | a0095 | c0054 | t0002 | g0052 | SAS | GIH | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01123 | hp1 | a0013 | c0010 | t0002 | g0075 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG01123 | hp2 | a0001 | c0006 | t0001 | g0145 | AMR | CLM | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02109 | hp2 | a0052 | c0174 | t0003 | g0097 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02486 | hp1 | a0024 | c0023 | t0003 | g0152 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02486 | hp2 | a0007 | c0016 | t0006 | g0087 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02559 | hp1 | a0056 | c0071 | t0005 | g0214 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG02559 | hp2 | a0057 | c0082 | t0005 | g0291 | AFR | ACB | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03471 | hp1 | a0072 | c0158 | t0004 | g0007 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG03471 | hp2 | a0009 | c0007 | t0005 | g0083 | AFR | MSL | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG06807 | hp1 | a0004 | c0025 | t0003 | g0094 | AFR | USA | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
HG06807 | hp2 | a0078 | c0100 | t0002 | g0154 | AFR | USA | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18955 | hp1 | a0083 | c0130 | t0001 | g0251 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA18955 | hp2 | a0084 | c0102 | t0002 | g0149 | EAS | JPT | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0235 | AFR | USA | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA20300 | hp2 | a0026 | c0033 | t0001 | g0084 | AFR | USA | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | LWK | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
NA21309 | hp2 | a0007 | c0035 | t0003 | g0099 | AFR | LWK | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
homoSapiens | chm13v2 | a0001 | c0028 | t0001 | g0167 | REF | REF | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0187 | REF | REF | PLEC_chr8_143910153_143978529 | PLEC | chr8 | 143910153 | 143978529 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143916323 | C | T | 1 | a0092 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.13456G>A | p.Gly4486Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13513/14683 | 13456/13602 | 4486/4533 | chr8 | 143916323 | |||
chr8:143916419 | C | T | 1 | a0072 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.13360G>A | p.Ala4454Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13417/14683 | 13360/13602 | 4454/4533 | chr8 | 143916419 | |||
chr8:143916616 | G | A | 2 | a0020 a0078 |
3 | HG01070.hp2 HG01071.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.13163C>T | p.Thr4388Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13220/14683 | 13163/13602 | 4388/4533 | chr8 | 143916616 | |||
chr8:143917037 | C | T | 1 | a0023 | 2 | HG02015.hp1 HG02074.hp2 |
missense_variant | MODERATE | c.12742G>A | p.Val4248Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12799/14683 | 12742/13602 | 4248/4533 | chr8 | 143917037 | |||
chr8:143917103 | C | T | 1 | a0038 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.12676G>A | p.Ala4226Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12733/14683 | 12676/13602 | 4226/4533 | chr8 | 143917103 | |||
chr8:143917174 | C | T | 1 | a0083 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.12605G>A | p.Arg4202His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12662/14683 | 12605/13602 | 4202/4533 | chr8 | 143917174 | |||
chr8:143917757 | G | A | 2 | a0033 a0034 |
2 | HG00621.hp2 HG00673.hp1 |
missense_variant | MODERATE | c.12022C>T | p.Leu4008Phe | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12079/14683 | 12022/13602 | 4008/4533 | chr8 | 143917757 | |||
chr8:143917993 | G | T | 1 | a0082 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.11786C>A | p.Thr3929Asn | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11843/14683 | 11786/13602 | 3929/4533 | chr8 | 143917993 | |||
chr8:143918101 | G | A | 3 | a0018 a0019 a0058 |
5 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(2): Show |
missense_variant | MODERATE | c.11678C>T | p.Thr3893Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11735/14683 | 11678/13602 | 3893/4533 | chr8 | 143918101 | |||
chr8:143918210 | C | T | 1 | a0030 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.11569G>A | p.Gly3857Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11626/14683 | 11569/13602 | 3857/4533 | chr8 | 143918210 | |||
chr8:143918222 | C | G | 8 | a0009 a0010 a0021 others(5): Show |
15 | HG01109.hp1 HG01175.hp1 HG02145.hp2 others(12): Show |
missense_variant | MODERATE | c.11557G>C | p.Asp3853His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11614/14683 | 11557/13602 | 3853/4533 | chr8 | 143918222 | |||
chr8:143918378 | C | G | 1 | a0043 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.11401G>C | p.Gly3801Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11458/14683 | 11401/13602 | 3801/4533 | chr8 | 143918378 | |||
chr8:143918684 | C | T | 1 | a0008 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.11095G>A | p.Gly3699Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11152/14683 | 11095/13602 | 3699/4533 | chr8 | 143918684 | |||
chr8:143918861 | C | T | 2 | a0085 a0092 |
2 | NA19011.hp1 NA19091.hp2 |
missense_variant | MODERATE | c.10918G>A | p.Glu3640Lys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10975/14683 | 10918/13602 | 3640/4533 | chr8 | 143918861 | |||
chr8:143918900 | C | T | 1 | a0050 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.10879G>A | p.Asp3627Asn | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10936/14683 | 10879/13602 | 3627/4533 | chr8 | 143918900 | |||
chr8:143919349 | C | T | 2 | a0033 a0034 |
2 | HG00621.hp2 HG00673.hp1 |
missense_variant | MODERATE | c.10430G>A | p.Arg3477His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10487/14683 | 10430/13602 | 3477/4533 | chr8 | 143919349 | |||
chr8:143919613 | C | T | 1 | a0081 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.10166G>A | p.Arg3389Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10223/14683 | 10166/13602 | 3389/4533 | chr8 | 143919613 | |||
chr8:143919691 | C | T | 1 | a0080 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.10088G>A | p.Arg3363Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10145/14683 | 10088/13602 | 3363/4533 | chr8 | 143919691 | |||
chr8:143919749 | C | T | 1 | a0074 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.10030G>A | p.Ala3344Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10087/14683 | 10030/13602 | 3344/4533 | chr8 | 143919749 | |||
chr8:143919775 | G | A | 5 | a0007 a0058 a0061 others(2): Show |
10 | HG02486.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
missense_variant | MODERATE | c.10004C>T | p.Thr3335Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10061/14683 | 10004/13602 | 3335/4533 | chr8 | 143919775 | |||
chr8:143919860 | C | T | 2 | a0008 a0028 |
2 | HG00099.hp2 HG01496.hp2 |
missense_variant | MODERATE | c.9919G>A | p.Gly3307Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9976/14683 | 9919/13602 | 3307/4533 | chr8 | 143919860 | |||
chr8:143919892 | G | A | 1 | a0041 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.9887C>T | p.Ala3296Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9944/14683 | 9887/13602 | 3296/4533 | chr8 | 143919892 | |||
chr8:143919926 | G | A | 1 | a0043 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.9853C>T | p.Arg3285Trp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9910/14683 | 9853/13602 | 3285/4533 | chr8 | 143919926 | |||
chr8:143920103 | C | T | 1 | a0079 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.9676G>A | p.Glu3226Lys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9733/14683 | 9676/13602 | 3226/4533 | chr8 | 143920103 | |||
chr8:143920346 | C | T | 1 | a0038 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.9433G>A | p.Ala3145Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9490/14683 | 9433/13602 | 3145/4533 | chr8 | 143920346 | |||
chr8:143920441 | C | T | 1 | a0087 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.9338G>A | p.Arg3113Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9395/14683 | 9338/13602 | 3113/4533 | chr8 | 143920441 | |||
chr8:143920513 | G | A | 1 | a0026 | 2 | HG02818.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.9266C>T | p.Thr3089Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9323/14683 | 9266/13602 | 3089/4533 | chr8 | 143920513 | |||
chr8:143920720 | G | A | 3 | a0008 a0013 a0028 |
5 | HG00099.hp2 HG00735.hp1 HG01109.hp2 others(2): Show |
missense_variant | MODERATE | c.9059C>T | p.Ala3020Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9116/14683 | 9059/13602 | 3020/4533 | chr8 | 143920720 | |||
chr8:143920748 | C | T | 10 | a0004 a0010 a0021 others(7): Show |
27 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(24): Show |
missense_variant | MODERATE | c.9031G>A | p.Val3011Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9088/14683 | 9031/13602 | 3011/4533 | chr8 | 143920748 | |||
chr8:143920750 | T | C | 1 | a0047 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.9029A>G | p.Asn3010Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9086/14683 | 9029/13602 | 3010/4533 | chr8 | 143920750 | |||
chr8:143920985 | G | A | 1 | a0075 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.8794C>T | p.Arg2932Cys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8851/14683 | 8794/13602 | 2932/4533 | chr8 | 143920985 | |||
chr8:143921001 | G | C | 10 | a0005 a0016 a0060 others(7): Show |
23 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(20): Show |
missense_variant | MODERATE | c.8778C>G | p.Asp2926Glu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8835/14683 | 8778/13602 | 2926/4533 | chr8 | 143921001 | |||
chr8:143921155 | G | A | 1 | a0045 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.8624C>T | p.Ala2875Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8681/14683 | 8624/13602 | 2875/4533 | chr8 | 143921155 | |||
chr8:143921233 | G | A | 1 | a0086 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.8546C>T | p.Thr2849Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8603/14683 | 8546/13602 | 2849/4533 | chr8 | 143921233 | |||
chr8:143921326 | C | T | 22 | a0002 a0008 a0013 others(19): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
missense_variant | MODERATE | c.8453G>A | p.Arg2818His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8510/14683 | 8453/13602 | 2818/4533 | chr8 | 143921326 | |||
chr8:143921332 | T | C | 2 | a0042 a0094 |
2 | HG01516.hp1 NA20805.hp2 |
missense_variant | MODERATE | c.8447A>G | p.Tyr2816Cys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8504/14683 | 8447/13602 | 2816/4533 | chr8 | 143921332 | |||
chr8:143921391 | G | C | 2 | a0039 a0064 |
2 | HG01346.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.8388C>G | p.Ile2796Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8445/14683 | 8388/13602 | 2796/4533 | chr8 | 143921391 | |||
chr8:143921771 | G | A | 2 | a0017 a0060 |
2 | HG00323.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.8008C>T | p.Arg2670Trp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8065/14683 | 8008/13602 | 2670/4533 | chr8 | 143921771 | |||
chr8:143921771 | G | C | 1 | a0017 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.8008C>G | p.Arg2670Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8065/14683 | 8008/13602 | 2670/4533 | chr8 | 143921771 | |||
chr8:143921809 | C | T | 2 | a0065 a0093 |
2 | HG02922.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.7970G>A | p.Arg2657Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8027/14683 | 7970/13602 | 2657/4533 | chr8 | 143921809 | |||
chr8:143921861 | A | G | 56 | a0002 a0004 a0005 others(53): Show |
152 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(149): Show |
missense_variant | MODERATE | c.7918T>C | p.Ser2640Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7975/14683 | 7918/13602 | 2640/4533 | chr8 | 143921861 | |||
chr8:143921870 | G | A | 1 | a0077 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.7909C>T | p.Arg2637Trp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7966/14683 | 7909/13602 | 2637/4533 | chr8 | 143921870 | |||
chr8:143922068 | C | G | 1 | a0027 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.7711G>C | p.Glu2571Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7768/14683 | 7711/13602 | 2571/4533 | chr8 | 143922068 | |||
chr8:143922118 | C | T | 1 | a0070 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.7661G>A | p.Arg2554His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7718/14683 | 7661/13602 | 2554/4533 | chr8 | 143922118 | |||
chr8:143922560 | G | A | 1 | a0020 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.7327C>T | p.Arg2443Cys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7384/14683 | 7327/13602 | 2443/4533 | chr8 | 143922560 | |||
chr8:143922823 | T | G | 1 | a0038 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.7064A>C | p.Glu2355Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7121/14683 | 7064/13602 | 2355/4533 | chr8 | 143922823 | |||
chr8:143923172 | C | T | 1 | a0049 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.6715G>A | p.Ala2239Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6772/14683 | 6715/13602 | 2239/4533 | chr8 | 143923172 | |||
chr8:143923393 | C | T | 1 | a0035 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.6494G>A | p.Arg2165Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6551/14683 | 6494/13602 | 2165/4533 | chr8 | 143923393 | |||
chr8:143923487 | G | A | 1 | a0032 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.6400C>T | p.Arg2134Trp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6457/14683 | 6400/13602 | 2134/4533 | chr8 | 143923487 | |||
chr8:143923615 | G | A | 3 | a0003 a0006 a0045 |
16 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
missense_variant | MODERATE | c.6272C>T | p.Ala2091Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6329/14683 | 6272/13602 | 2091/4533 | chr8 | 143923615 | |||
chr8:143923618 | G | A | 2 | a0063 a0095 |
2 | HG02738.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.6269C>T | p.Ala2090Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6326/14683 | 6269/13602 | 2090/4533 | chr8 | 143923618 | |||
chr8:143923759 | G | A | 22 | a0002 a0008 a0013 others(19): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
missense_variant | MODERATE | c.6128C>T | p.Ala2043Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6185/14683 | 6128/13602 | 2043/4533 | chr8 | 143923759 | |||
chr8:143923855 | C | T | 1 | a0057 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.6032G>A | p.Arg2011Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6089/14683 | 6032/13602 | 2011/4533 | chr8 | 143923855 | |||
chr8:143923870 | T | G | 1 | a0095 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.6017A>C | p.Glu2006Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6074/14683 | 6017/13602 | 2006/4533 | chr8 | 143923870 | |||
chr8:143923928 | C | T | 1 | a0042 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.5959G>A | p.Ala1987Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6016/14683 | 5959/13602 | 1987/4533 | chr8 | 143923928 | |||
chr8:143923978 | C | T | 1 | a0006 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.5909G>A | p.Arg1970His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5966/14683 | 5909/13602 | 1970/4533 | chr8 | 143923978 | |||
chr8:143924003 | C | T | 1 | a0059 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.5884G>A | p.Ala1962Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5941/14683 | 5884/13602 | 1962/4533 | chr8 | 143924003 | |||
chr8:143924007 | C | G | 1 | a0039 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.5880G>C | p.Gln1960His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5937/14683 | 5880/13602 | 1960/4533 | chr8 | 143924007 | |||
chr8:143924020 | G | A | 1 | a0071 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.5867C>T | p.Ala1956Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5924/14683 | 5867/13602 | 1956/4533 | chr8 | 143924020 | |||
chr8:143924056 | G | A | 1 | a0019 | 2 | HG00741.hp1 HG01070.hp1 |
missense_variant | MODERATE | c.5831C>T | p.Thr1944Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5888/14683 | 5831/13602 | 1944/4533 | chr8 | 143924056 | |||
chr8:143924114 | C | T | 1 | a0062 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.5773G>A | p.Ala1925Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5830/14683 | 5773/13602 | 1925/4533 | chr8 | 143924114 | |||
chr8:143924248 | C | T | 1 | a0051 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.5639G>A | p.Arg1880His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5696/14683 | 5639/13602 | 1880/4533 | chr8 | 143924248 | |||
chr8:143924276 | C | T | 2 | a0015 a0086 |
4 | HG02080.hp2 NA18947.hp1 NA18954.hp1 others(1): Show |
missense_variant | MODERATE | c.5611G>A | p.Ala1871Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5668/14683 | 5611/13602 | 1871/4533 | chr8 | 143924276 | |||
chr8:143924716 | C | T | 1 | a0046 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.5171G>A | p.Arg1724Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5228/14683 | 5171/13602 | 1724/4533 | chr8 | 143924716 | |||
chr8:143924764 | G | A | 1 | a0065 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.5123C>T | p.Thr1708Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5180/14683 | 5123/13602 | 1708/4533 | chr8 | 143924764 | |||
chr8:143925056 | C | T | 2 | a0054 a0066 |
2 | HG02258.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.4831G>A | p.Glu1611Lys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4888/14683 | 4831/13602 | 1611/4533 | chr8 | 143925056 | |||
chr8:143925061 | G | GC | 9 | a0006 a0008 a0021 others(6): Show |
22 | HG00423.hp2 HG00673.hp1 HG01192.hp1 others(19): Show |
frameshift_variant | HIGH | c.4825dupG | p.Ala1609fs | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4882/14683 | 4825/13602 | 1609/4533 | chr8 | 143925061 | |||
chr8:143925224 | T | C | 2 | a0058 a0073 |
2 | HG02572.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.4663A>G | p.Thr1555Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4720/14683 | 4663/13602 | 1555/4533 | chr8 | 143925224 | |||
chr8:143925278 | G | A | 2 | a0036 a0084 |
2 | HG01081.hp2 NA18955.hp2 |
missense_variant | MODERATE | c.4609C>T | p.Arg1537Cys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4666/14683 | 4609/13602 | 1537/4533 | chr8 | 143925278 | |||
chr8:143925331 | C | T | 2 | a0020 a0078 |
3 | HG01070.hp2 HG01071.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.4556G>A | p.Arg1519Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4613/14683 | 4556/13602 | 1519/4533 | chr8 | 143925331 | |||
chr8:143925332 | G | A | 2 | a0089 a0091 |
2 | NA19057.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.4555C>T | p.Arg1519Trp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4612/14683 | 4555/13602 | 1519/4533 | chr8 | 143925332 | |||
chr8:143925563 | C | T | 1 | a0019 | 2 | HG00741.hp1 HG01070.hp1 |
missense_variant | MODERATE | c.4324G>A | p.Val1442Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4381/14683 | 4324/13602 | 1442/4533 | chr8 | 143925563 | |||
chr8:143925706 | G | A | 3 | a0058 a0061 a0073 |
3 | HG02572.hp1 HG02723.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.4181C>T | p.Ala1394Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4238/14683 | 4181/13602 | 1394/4533 | chr8 | 143925706 | |||
chr8:143925767 | G | A | 2 | a0012 a0031 |
4 | HG00423.hp2 HG00438.hp1 NA18999.hp2 others(1): Show |
missense_variant | MODERATE | c.4120C>T | p.Arg1374Trp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4177/14683 | 4120/13602 | 1374/4533 | chr8 | 143925767 | |||
chr8:143926863 | T | C | 55 | a0002 a0004 a0005 others(52): Show |
151 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(148): Show |
missense_variant | MODERATE | c.3923A>G | p.His1308Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/32 | 3980/14683 | 3923/13602 | 1308/4533 | chr8 | 143926863 | |||
chr8:143927305 | C | T | 1 | a0076 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.3745G>A | p.Glu1249Lys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/32 | 3802/14683 | 3745/13602 | 1249/4533 | chr8 | 143927305 | |||
chr8:143927314 | G | C | 1 | a0059 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.3736C>G | p.Arg1246Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/32 | 3793/14683 | 3736/13602 | 1246/4533 | chr8 | 143927314 | |||
chr8:143927420 | C | T | 21 | a0002 a0008 a0013 others(18): Show |
73 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(70): Show |
missense_variant | MODERATE | c.3704G>A | p.Arg1235Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/32 | 3761/14683 | 3704/13602 | 1235/4533 | chr8 | 143927420 | |||
chr8:143927546 | C | A | 1 | a0088 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.3578G>T | p.Arg1193Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/32 | 3635/14683 | 3578/13602 | 1193/4533 | chr8 | 143927546 | |||
chr8:143927732 | G | A | 1 | a0016 | 3 | HG02895.hp1 HG02896.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.3392C>T | p.Thr1131Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/32 | 3449/14683 | 3392/13602 | 1131/4533 | chr8 | 143927732 | |||
chr8:143929478 | C | T | 1 | a0048 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2975G>A | p.Arg992His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 24/32 | 3032/14683 | 2975/13602 | 992/4533 | chr8 | 143929478 | |||
chr8:143929971 | C | T | 1 | a0024 | 2 | HG02486.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.2662G>A | p.Asp888Asn | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 22/32 | 2719/14683 | 2662/13602 | 888/4533 | chr8 | 143929971 | |||
chr8:143930208 | C | T | 4 | a0009 a0010 a0021 others(1): Show |
12 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
missense_variant | MODERATE | c.2506G>A | p.Ala836Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 21/32 | 2563/14683 | 2506/13602 | 836/4533 | chr8 | 143930208 | |||
chr8:143931975 | T | C | 1 | a0033 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.2098A>G | p.Ile700Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 18/32 | 2155/14683 | 2098/13602 | 700/4533 | chr8 | 143931975 | |||
chr8:143932679 | G | A | 1 | a0044 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1729C>T | p.Arg577Cys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 15/32 | 1786/14683 | 1729/13602 | 577/4533 | chr8 | 143932679 | |||
chr8:143932824 | C | T | 1 | a0029 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1664G>A | p.Arg555Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 14/32 | 1721/14683 | 1664/13602 | 555/4533 | chr8 | 143932824 | |||
chr8:143932901 | C | A | 1 | a0052 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1587G>T | p.Glu529Asp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 14/32 | 1644/14683 | 1587/13602 | 529/4533 | chr8 | 143932901 | |||
chr8:143933019 | G | A | 21 | a0002 a0008 a0013 others(18): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
missense_variant | MODERATE | c.1469C>T | p.Ala490Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 14/32 | 1526/14683 | 1469/13602 | 490/4533 | chr8 | 143933019 | |||
chr8:143933044 | C | T | 1 | a0090 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.1444G>A | p.Val482Met | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 14/32 | 1501/14683 | 1444/13602 | 482/4533 | chr8 | 143933044 | |||
chr8:143933076 | C | A | 1 | a0053 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1412G>T | p.Arg471Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 14/32 | 1469/14683 | 1412/13602 | 471/4533 | chr8 | 143933076 | |||
chr8:143934854 | C | T | 1 | a0056 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.859G>A | p.Ala287Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 9/32 | 916/14683 | 859/13602 | 287/4533 | chr8 | 143934854 | |||
chr8:143934868 | C | T | 1 | a0022 | 2 | HG01256.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.845G>A | p.Arg282Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 9/32 | 902/14683 | 845/13602 | 282/4533 | chr8 | 143934868 | |||
chr8:143934901 | C | T | 1 | a0065 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.812G>A | p.Arg271Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 9/32 | 869/14683 | 812/13602 | 271/4533 | chr8 | 143934901 | |||
chr8:143935994 | A | C | 1 | a0055 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.414T>G | p.Ser138Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 6/32 | 471/14683 | 414/13602 | 138/4533 | chr8 | 143935994 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143916246 | C | T | 1 | a0001c0139 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.13533G>A | p.Ser4511Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13590/14683 | 13533/13602 | 4511/4533 | chr8 | 143916246 | |||
chr8:143916360 | A | G | 95 | a0001c0131 a0002c0002 a0002c0005 others(92): Show |
154 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(151): Show |
synonymous_variant | LOW | c.13419T>C | p.Ala4473Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13476/14683 | 13419/13602 | 4473/4533 | chr8 | 143916360 | |||
chr8:143916477 | G | A | 1 | a0030c0129 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.13302C>T | p.Asp4434Asp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13359/14683 | 13302/13602 | 4434/4533 | chr8 | 143916477 | |||
chr8:143916615 | C | T | 1 | a0001c0132 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.13164G>A | p.Thr4388Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13221/14683 | 13164/13602 | 4388/4533 | chr8 | 143916615 | |||
chr8:143916711 | G | A | 1 | a0001c0029 | 2 | HG01952.hp1 HG02004.hp2 |
synonymous_variant | LOW | c.13068C>T | p.Ala4356Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13125/14683 | 13068/13602 | 4356/4533 | chr8 | 143916711 | |||
chr8:143916753 | G | A | 1 | a0008c0055 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.13026C>T | p.Phe4342Phe | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 13083/14683 | 13026/13602 | 4342/4533 | chr8 | 143916753 | |||
chr8:143917008 | T | C | 95 | a0001c0131 a0002c0002 a0002c0005 others(92): Show |
154 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(151): Show |
synonymous_variant | LOW | c.12771A>G | p.Ser4257Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12828/14683 | 12771/13602 | 4257/4533 | chr8 | 143917008 | |||
chr8:143917260 | G | A | 19 | a0005c0003 a0005c0094 a0005c0095 others(16): Show |
33 | HG01109.hp1 HG01175.hp1 HG02145.hp2 others(30): Show |
synonymous_variant | LOW | c.12519C>T | p.Asp4173Asp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12576/14683 | 12519/13602 | 4173/4533 | chr8 | 143917260 | |||
chr8:143917272 | G | A | 1 | a0095c0054 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.12507C>T | p.Ile4169Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12564/14683 | 12507/13602 | 4169/4533 | chr8 | 143917272 | |||
chr8:143917461 | C | T | 1 | a0001c0140 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.12318G>A | p.Pro4106Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12375/14683 | 12318/13602 | 4106/4533 | chr8 | 143917461 | |||
chr8:143917578 | G | A | 1 | a0003c0114 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.12201C>T | p.Thr4067Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12258/14683 | 12201/13602 | 4067/4533 | chr8 | 143917578 | |||
chr8:143917605 | G | A | 1 | a0006c0152 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.12174C>T | p.Phe4058Phe | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 12231/14683 | 12174/13602 | 4058/4533 | chr8 | 143917605 | |||
chr8:143917881 | G | A | 1 | a0001c0080 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.11898C>T | p.Ile3966Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11955/14683 | 11898/13602 | 3966/4533 | chr8 | 143917881 | |||
chr8:143917908 | C | T | 10 | a0009c0007 a0010c0022 a0010c0083 others(7): Show |
15 | HG01109.hp1 HG01175.hp1 HG02145.hp2 others(12): Show |
synonymous_variant | LOW | c.11871G>A | p.Ala3957Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11928/14683 | 11871/13602 | 3957/4533 | chr8 | 143917908 | |||
chr8:143917935 | T | C | 96 | a0001c0127 a0001c0131 a0002c0002 others(93): Show |
155 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(152): Show |
synonymous_variant | LOW | c.11844A>G | p.Thr3948Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11901/14683 | 11844/13602 | 3948/4533 | chr8 | 143917935 | |||
chr8:143918193 | T | C | 96 | a0001c0013 a0001c0072 a0001c0131 others(93): Show |
157 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(154): Show |
synonymous_variant | LOW | c.11586A>G | p.Pro3862Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11643/14683 | 11586/13602 | 3862/4533 | chr8 | 143918193 | |||
chr8:143918220 | G | A | 9 | a0001c0030 a0005c0003 a0005c0094 others(6): Show |
19 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(16): Show |
synonymous_variant | LOW | c.11559C>T | p.Asp3853Asp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11616/14683 | 11559/13602 | 3853/4533 | chr8 | 143918220 | |||
chr8:143918283 | G | A | 1 | a0004c0074 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.11496C>T | p.Tyr3832Tyr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11553/14683 | 11496/13602 | 3832/4533 | chr8 | 143918283 | |||
chr8:143918514 | G | A | 1 | a0076c0038 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.11265C>T | p.Thr3755Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11322/14683 | 11265/13602 | 3755/4533 | chr8 | 143918514 | |||
chr8:143918547 | G | A | 1 | a0014c0064 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.11232C>T | p.His3744His | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11289/14683 | 11232/13602 | 3744/4533 | chr8 | 143918547 | |||
chr8:143918613 | C | T | 2 | a0001c0128 a0001c0149 |
2 | HG02683.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.11166G>A | p.Pro3722Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11223/14683 | 11166/13602 | 3722/4533 | chr8 | 143918613 | |||
chr8:143918694 | A | G | 87 | a0002c0002 a0002c0005 a0002c0037 others(84): Show |
139 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(136): Show |
synonymous_variant | LOW | c.11085T>C | p.Ala3695Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11142/14683 | 11085/13602 | 3695/4533 | chr8 | 143918694 | |||
chr8:143918732 | G | A | 2 | a0001c0132 a0049c0120 |
2 | HG02055.hp2 HG03017.hp1 |
synonymous_variant | LOW | c.11047C>T | p.Leu3683Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11104/14683 | 11047/13602 | 3683/4533 | chr8 | 143918732 | |||
chr8:143918778 | G | A | 1 | a0001c0104 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.11001C>T | p.Ser3667Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 11058/14683 | 11001/13602 | 3667/4533 | chr8 | 143918778 | |||
chr8:143918901 | G | A | 2 | a0001c0133 a0029c0077 |
2 | HG00140.hp2 HG01928.hp1 |
synonymous_variant | LOW | c.10878C>T | p.Tyr3626Tyr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10935/14683 | 10878/13602 | 3626/4533 | chr8 | 143918901 | |||
chr8:143919156 | C | T | 38 | a0001c0127 a0002c0002 a0002c0005 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.10623G>A | p.Thr3541Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10680/14683 | 10623/13602 | 3541/4533 | chr8 | 143919156 | |||
chr8:143919209 | A | G | 94 | a0002c0002 a0002c0005 a0002c0019 others(91): Show |
154 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(151): Show |
synonymous_variant | LOW | c.10570T>C | p.Leu3524Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10627/14683 | 10570/13602 | 3524/4533 | chr8 | 143919209 | |||
chr8:143919255 | C | T | 2 | a0058c0163 a0073c0162 |
2 | HG02572.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.10524G>A | p.Thr3508Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10581/14683 | 10524/13602 | 3508/4533 | chr8 | 143919255 | |||
chr8:143919390 | G | C | 1 | a0040c0061 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.10389C>G | p.Pro3463Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10446/14683 | 10389/13602 | 3463/4533 | chr8 | 143919390 | |||
chr8:143919405 | G | A | 1 | a0084c0102 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.10374C>T | p.Gly3458Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10431/14683 | 10374/13602 | 3458/4533 | chr8 | 143919405 | |||
chr8:143919483 | G | A | 1 | a0005c0095 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.10296C>T | p.Ser3432Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10353/14683 | 10296/13602 | 3432/4533 | chr8 | 143919483 | |||
chr8:143919573 | G | A | 1 | a0077c0142 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.10206C>T | p.Gly3402Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10263/14683 | 10206/13602 | 3402/4533 | chr8 | 143919573 | |||
chr8:143919618 | G | A | 1 | a0014c0062 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.10161C>T | p.Pro3387Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10218/14683 | 10161/13602 | 3387/4533 | chr8 | 143919618 | |||
chr8:143919795 | C | T | 1 | a0082c0134 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.9984G>A | p.Ser3328Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10041/14683 | 9984/13602 | 3328/4533 | chr8 | 143919795 | |||
chr8:143919807 | G | A | 5 | a0005c0003 a0005c0095 a0005c0098 others(2): Show |
12 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.9972C>T | p.Val3324Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10029/14683 | 9972/13602 | 3324/4533 | chr8 | 143919807 | |||
chr8:143919855 | G | A | 3 | a0007c0035 a0060c0159 a0071c0160 |
4 | HG02717.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.9924C>T | p.Val3308Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9981/14683 | 9924/13602 | 3308/4533 | chr8 | 143919855 | |||
chr8:143919876 | G | A | 3 | a0039c0111 a0065c0070 a0093c0078 |
3 | HG01346.hp1 HG02922.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.9903C>T | p.Ser3301Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9960/14683 | 9903/13602 | 3301/4533 | chr8 | 143919876 | |||
chr8:143919993 | C | T | 1 | a0006c0152 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.9786G>A | p.Thr3262Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9843/14683 | 9786/13602 | 3262/4533 | chr8 | 143919993 | |||
chr8:143920044 | A | T | 25 | a0004c0008 a0004c0073 a0004c0074 others(22): Show |
33 | HG01192.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
synonymous_variant | LOW | c.9735T>A | p.Ser3245Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9792/14683 | 9735/13602 | 3245/4533 | chr8 | 143920044 | |||
chr8:143920179 | T | C | 1 | a0002c0049 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.9600A>G | p.Glu3200Glu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9657/14683 | 9600/13602 | 3200/4533 | chr8 | 143920179 | |||
chr8:143920310 | G | A | 1 | a0014c0064 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.9469C>T | p.Leu3157Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9526/14683 | 9469/13602 | 3157/4533 | chr8 | 143920310 | |||
chr8:143920386 | G | A | 1 | a0005c0167 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.9393C>T | p.Asp3131Asp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9450/14683 | 9393/13602 | 3131/4533 | chr8 | 143920386 | |||
chr8:143920398 | G | A | 9 | a0001c0013 a0001c0031 a0001c0072 others(6): Show |
12 | HG02015.hp1 HG02027.hp1 HG02074.hp2 others(9): Show |
synonymous_variant | LOW | c.9381C>T | p.Gly3127Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9438/14683 | 9381/13602 | 3127/4533 | chr8 | 143920398 | |||
chr8:143920413 | G | A | 3 | a0001c0032 a0033c0066 a0034c0101 |
4 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(1): Show |
synonymous_variant | LOW | c.9366C>T | p.Ala3122Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9423/14683 | 9366/13602 | 3122/4533 | chr8 | 143920413 | |||
chr8:143920479 | G | A | 1 | a0001c0136 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.9300C>T | p.Val3100Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 9357/14683 | 9300/13602 | 3100/4533 | chr8 | 143920479 | |||
chr8:143920839 | G | A | 1 | a0069c0097 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.8940C>T | p.Arg2980Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8997/14683 | 8940/13602 | 2980/4533 | chr8 | 143920839 | |||
chr8:143921124 | G | A | 2 | a0001c0072 a0002c0051 |
2 | HG01261.hp2 NA19081.hp1 |
synonymous_variant | LOW | c.8655C>T | p.Ser2885Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8712/14683 | 8655/13602 | 2885/4533 | chr8 | 143921124 | |||
chr8:143921376 | A | G | 1 | a0047c0143 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.8403T>C | p.Val2801Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8460/14683 | 8403/13602 | 2801/4533 | chr8 | 143921376 | |||
chr8:143921379 | G | A | 1 | a0001c0139 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.8400C>T | p.Gly2800Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8457/14683 | 8400/13602 | 2800/4533 | chr8 | 143921379 | |||
chr8:143921502 | G | A | 11 | a0004c0025 a0004c0096 a0005c0003 others(8): Show |
21 | HG02280.hp2 HG02300.hp1 HG02622.hp1 others(18): Show |
synonymous_variant | LOW | c.8277C>T | p.Ala2759Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8334/14683 | 8277/13602 | 2759/4533 | chr8 | 143921502 | |||
chr8:143921568 | G | A | 39 | a0001c0171 a0002c0002 a0002c0005 others(36): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
synonymous_variant | LOW | c.8211C>T | p.Asn2737Asn | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8268/14683 | 8211/13602 | 2737/4533 | chr8 | 143921568 | |||
chr8:143921796 | G | A | 4 | a0001c0140 a0001c0141 a0006c0034 others(1): Show |
6 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
synonymous_variant | LOW | c.7983C>T | p.Gly2661Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8040/14683 | 7983/13602 | 2661/4533 | chr8 | 143921796 | |||
chr8:143921802 | C | T | 1 | a0002c0059 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.7977G>A | p.Ala2659Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 8034/14683 | 7977/13602 | 2659/4533 | chr8 | 143921802 | |||
chr8:143921943 | C | T | 11 | a0001c0028 a0003c0004 a0003c0105 others(8): Show |
18 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(15): Show |
synonymous_variant | LOW | c.7836G>A | p.Leu2612Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7893/14683 | 7836/13602 | 2612/4533 | chr8 | 143921943 | |||
chr8:143922095 | G | A | 11 | a0004c0025 a0004c0096 a0005c0003 others(8): Show |
21 | HG02280.hp2 HG02300.hp1 HG02622.hp1 others(18): Show |
synonymous_variant | LOW | c.7684C>T | p.Leu2562Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7741/14683 | 7684/13602 | 2562/4533 | chr8 | 143922095 | |||
chr8:143922240 | T | G | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.7539A>C | p.Ala2513Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7596/14683 | 7539/13602 | 2513/4533 | chr8 | 143922240 | |||
chr8:143922309 | C | T | 1 | a0023c0123 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.7470G>A | p.Gln2490Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7527/14683 | 7470/13602 | 2490/4533 | chr8 | 143922309 | |||
chr8:143922315 | C | T | 1 | a0001c0122 | 1 | NA18945.hp2 | synonymous_variant | LOW | c.7464G>A | p.Leu2488Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 7521/14683 | 7464/13602 | 2488/4533 | chr8 | 143922315 | |||
chr8:143922663 | G | A | 4 | a0001c0006 a0001c0009 a0001c0171 others(1): Show |
12 | HG00621.hp1 HG01123.hp2 HG01358.hp1 others(9): Show |
synonymous_variant | LOW | c.7224C>T | p.Leu2408Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7281/14683 | 7224/13602 | 2408/4533 | chr8 | 143922663 | |||
chr8:143922669 | C | T | 2 | a0025c0020 a0053c0067 |
3 | HG02145.hp1 HG02622.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.7218G>A | p.Thr2406Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7275/14683 | 7218/13602 | 2406/4533 | chr8 | 143922669 | |||
chr8:143922735 | G | A | 1 | a0002c0053 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.7152C>T | p.Arg2384Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7209/14683 | 7152/13602 | 2384/4533 | chr8 | 143922735 | |||
chr8:143922819 | G | A | 4 | a0005c0167 a0011c0169 a0060c0159 others(1): Show |
4 | HG02717.hp1 HG02976.hp2 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.7068C>T | p.Ala2356Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7125/14683 | 7068/13602 | 2356/4533 | chr8 | 143922819 | |||
chr8:143922831 | C | A | 1 | a0010c0084 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.7056G>T | p.Arg2352Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7113/14683 | 7056/13602 | 2352/4533 | chr8 | 143922831 | |||
chr8:143922855 | C | T | 1 | a0002c0041 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.7032G>A | p.Ala2344Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7089/14683 | 7032/13602 | 2344/4533 | chr8 | 143922855 | |||
chr8:143922900 | C | T | 1 | a0001c0121 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.6987G>A | p.Ala2329Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 7044/14683 | 6987/13602 | 2329/4533 | chr8 | 143922900 | |||
chr8:143923173 | G | A | 1 | a0001c0145 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.6714C>T | p.Arg2238Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6771/14683 | 6714/13602 | 2238/4533 | chr8 | 143923173 | |||
chr8:143923188 | G | A | 5 | a0007c0016 a0007c0075 a0058c0163 others(2): Show |
7 | HG02486.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
synonymous_variant | LOW | c.6699C>T | p.Ile2233Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6756/14683 | 6699/13602 | 2233/4533 | chr8 | 143923188 | |||
chr8:143923302 | C | T | 1 | a0010c0083 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.6585G>A | p.Leu2195Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6642/14683 | 6585/13602 | 2195/4533 | chr8 | 143923302 | |||
chr8:143923352 | G | A | 2 | a0065c0070 a0093c0078 |
2 | HG02922.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.6535C>T | p.Leu2179Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6592/14683 | 6535/13602 | 2179/4533 | chr8 | 143923352 | |||
chr8:143923422 | C | T | 1 | a0014c0062 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.6465G>A | p.Lys2155Lys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6522/14683 | 6465/13602 | 2155/4533 | chr8 | 143923422 | |||
chr8:143923488 | C | T | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.6399G>A | p.Ala2133Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6456/14683 | 6399/13602 | 2133/4533 | chr8 | 143923488 | |||
chr8:143923521 | C | T | 2 | a0004c0086 a0004c0175 |
2 | HG02647.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.6366G>A | p.Glu2122Glu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6423/14683 | 6366/13602 | 2122/4533 | chr8 | 143923521 | |||
chr8:143923611 | C | T | 1 | a0003c0113 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.6276G>A | p.Gln2092Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6333/14683 | 6276/13602 | 2092/4533 | chr8 | 143923611 | |||
chr8:143923833 | C | T | 1 | a0001c0118 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.6054G>A | p.Ser2018Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 6111/14683 | 6054/13602 | 2018/4533 | chr8 | 143923833 | |||
chr8:143924001 | C | T | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.5886G>A | p.Ala1962Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5943/14683 | 5886/13602 | 1962/4533 | chr8 | 143924001 | |||
chr8:143924022 | A | G | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.5865T>C | p.Ala1955Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5922/14683 | 5865/13602 | 1955/4533 | chr8 | 143924022 | |||
chr8:143924064 | C | T | 10 | a0004c0025 a0004c0096 a0005c0003 others(7): Show |
20 | HG02280.hp2 HG02300.hp1 HG02622.hp1 others(17): Show |
synonymous_variant | LOW | c.5823G>A | p.Ala1941Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5880/14683 | 5823/13602 | 1941/4533 | chr8 | 143924064 | |||
chr8:143924217 | G | A | 1 | a0059c0103 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.5670C>T | p.Ser1890Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5727/14683 | 5670/13602 | 1890/4533 | chr8 | 143924217 | |||
chr8:143924256 | G | A | 1 | a0080c0147 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.5631C>T | p.Ile1877Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5688/14683 | 5631/13602 | 1877/4533 | chr8 | 143924256 | |||
chr8:143924346 | C | T | 11 | a0001c0112 a0003c0004 a0003c0105 others(8): Show |
18 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(15): Show |
synonymous_variant | LOW | c.5541G>A | p.Ala1847Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5598/14683 | 5541/13602 | 1847/4533 | chr8 | 143924346 | |||
chr8:143924409 | G | A | 1 | a0003c0148 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.5478C>T | p.Ala1826Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5535/14683 | 5478/13602 | 1826/4533 | chr8 | 143924409 | |||
chr8:143924613 | C | T | 8 | a0004c0008 a0004c0073 a0004c0074 others(5): Show |
13 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(10): Show |
synonymous_variant | LOW | c.5274G>A | p.Ala1758Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5331/14683 | 5274/13602 | 1758/4533 | chr8 | 143924613 | |||
chr8:143924625 | C | T | 1 | a0003c0110 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.5262G>A | p.Leu1754Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5319/14683 | 5262/13602 | 1754/4533 | chr8 | 143924625 | |||
chr8:143924643 | G | A | 1 | a0004c0096 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.5244C>T | p.Ala1748Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5301/14683 | 5244/13602 | 1748/4533 | chr8 | 143924643 | |||
chr8:143924700 | C | T | 2 | a0003c0004 a0045c0109 |
9 | HG00639.hp2 HG01074.hp1 HG01167.hp2 others(6): Show |
synonymous_variant | LOW | c.5187G>A | p.Ala1729Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 5244/14683 | 5187/13602 | 1729/4533 | chr8 | 143924700 | |||
chr8:143925012 | G | A | 1 | a0001c0149 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.4875C>T | p.Asn1625Asn | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4932/14683 | 4875/13602 | 1625/4533 | chr8 | 143925012 | |||
chr8:143925075 | G | A | 1 | a0052c0174 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.4812C>T | p.Ala1604Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4869/14683 | 4812/13602 | 1604/4533 | chr8 | 143925075 | |||
chr8:143925219 | C | T | 1 | a0032c0108 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.4668G>A | p.Ala1556Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4725/14683 | 4668/13602 | 1556/4533 | chr8 | 143925219 | |||
chr8:143925249 | C | T | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.4638G>A | p.Ala1546Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4695/14683 | 4638/13602 | 1546/4533 | chr8 | 143925249 | |||
chr8:143925285 | C | T | 17 | a0004c0008 a0004c0073 a0004c0074 others(14): Show |
22 | HG01192.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
synonymous_variant | LOW | c.4602G>A | p.Ala1534Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4659/14683 | 4602/13602 | 1534/4533 | chr8 | 143925285 | |||
chr8:143925294 | C | T | 1 | a0005c0167 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.4593G>A | p.Ala1531Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4650/14683 | 4593/13602 | 1531/4533 | chr8 | 143925294 | |||
chr8:143925369 | G | A | 1 | a0002c0058 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.4518C>T | p.Arg1506Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4575/14683 | 4518/13602 | 1506/4533 | chr8 | 143925369 | |||
chr8:143925372 | C | T | 3 | a0015c0107 a0065c0070 a0093c0078 |
3 | HG02922.hp2 NA18954.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.4515G>A | p.Ser1505Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4572/14683 | 4515/13602 | 1505/4533 | chr8 | 143925372 | |||
chr8:143925414 | G | A | 1 | a0005c0098 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.4473C>T | p.Asp1491Asp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4530/14683 | 4473/13602 | 1491/4533 | chr8 | 143925414 | |||
chr8:143925453 | C | T | 36 | a0002c0002 a0002c0019 a0002c0037 others(33): Show |
66 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(63): Show |
synonymous_variant | LOW | c.4434G>A | p.Ala1478Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4491/14683 | 4434/13602 | 1478/4533 | chr8 | 143925453 | |||
chr8:143925474 | A | C | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.4413T>G | p.Ala1471Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4470/14683 | 4413/13602 | 1471/4533 | chr8 | 143925474 | |||
chr8:143925516 | A | G | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.4371T>C | p.Ala1457Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4428/14683 | 4371/13602 | 1457/4533 | chr8 | 143925516 | |||
chr8:143925708 | C | T | 1 | a0001c0106 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.4179G>A | p.Ala1393Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4236/14683 | 4179/13602 | 1393/4533 | chr8 | 143925708 | |||
chr8:143925846 | C | T | 1 | a0003c0105 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.4041G>A | p.Arg1347Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/32 | 4098/14683 | 4041/13602 | 1347/4533 | chr8 | 143925846 | |||
chr8:143927058 | C | T | 1 | a0001c0104 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.3822G>A | p.Thr1274Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 29/32 | 3879/14683 | 3822/13602 | 1274/4533 | chr8 | 143927058 | |||
chr8:143927318 | G | A | 1 | a0002c0060 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.3732C>T | p.Ile1244Ile | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/32 | 3789/14683 | 3732/13602 | 1244/4533 | chr8 | 143927318 | |||
chr8:143927421 | G | T | 1 | a0059c0103 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.3703C>A | p.Arg1235Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/32 | 3760/14683 | 3703/13602 | 1235/4533 | chr8 | 143927421 | |||
chr8:143927449 | G | A | 12 | a0004c0008 a0004c0073 a0004c0074 others(9): Show |
17 | HG01516.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
synonymous_variant | LOW | c.3675C>T | p.Ala1225Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/32 | 3732/14683 | 3675/13602 | 1225/4533 | chr8 | 143927449 | |||
chr8:143927616 | A | G | 38 | a0002c0002 a0002c0005 a0002c0019 others(35): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.3508T>C | p.Leu1170Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/32 | 3565/14683 | 3508/13602 | 1170/4533 | chr8 | 143927616 | |||
chr8:143927623 | G | A | 1 | a0001c0166 | 1 | HG01258.hp2 | synonymous_variant | LOW | c.3501C>T | p.Val1167Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/32 | 3558/14683 | 3501/13602 | 1167/4533 | chr8 | 143927623 | |||
chr8:143927875 | C | T | 12 | a0004c0025 a0004c0096 a0005c0003 others(9): Show |
22 | HG02280.hp2 HG02300.hp1 HG02622.hp1 others(19): Show |
synonymous_variant | LOW | c.3336G>A | p.Glu1112Glu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 26/32 | 3393/14683 | 3336/13602 | 1112/4533 | chr8 | 143927875 | |||
chr8:143927902 | G | A | 1 | a0002c0065 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.3309C>T | p.Ala1103Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 26/32 | 3366/14683 | 3309/13602 | 1103/4533 | chr8 | 143927902 | |||
chr8:143929171 | G | A | 3 | a0005c0167 a0011c0169 a0079c0168 |
3 | HG02976.hp2 NA18522.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.3150C>T | p.Arg1050Arg | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/32 | 3207/14683 | 3150/13602 | 1050/4533 | chr8 | 143929171 | |||
chr8:143929534 | G | A | 1 | a0001c0036 | 2 | HG00280.hp2 HG00639.hp1 |
synonymous_variant | LOW | c.2919C>T | p.Ser973Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 24/32 | 2976/14683 | 2919/13602 | 973/4533 | chr8 | 143929534 | |||
chr8:143929659 | C | T | 1 | a0001c0024 | 2 | NA18962.hp2 NA19088.hp1 |
synonymous_variant | LOW | c.2868G>A | p.Gln956Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 23/32 | 2925/14683 | 2868/13602 | 956/4533 | chr8 | 143929659 | |||
chr8:143929695 | G | A | 1 | a0050c0170 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.2832C>T | p.Tyr944Tyr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 23/32 | 2889/14683 | 2832/13602 | 944/4533 | chr8 | 143929695 | |||
chr8:143929737 | G | A | 2 | a0001c0006 a0001c0171 |
7 | HG01123.hp2 HG01358.hp1 HG01934.hp2 others(4): Show |
synonymous_variant | LOW | c.2790C>T | p.Gly930Gly | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 23/32 | 2847/14683 | 2790/13602 | 930/4533 | chr8 | 143929737 | |||
chr8:143930017 | C | T | 15 | a0004c0008 a0004c0073 a0004c0074 others(12): Show |
20 | HG01884.hp1 HG01891.hp2 HG01975.hp1 others(17): Show |
synonymous_variant | LOW | c.2616G>A | p.Leu872Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 22/32 | 2673/14683 | 2616/13602 | 872/4533 | chr8 | 143930017 | |||
chr8:143930212 | C | T | 1 | a0001c0080 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.2502G>A | p.Glu834Glu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 21/32 | 2559/14683 | 2502/13602 | 834/4533 | chr8 | 143930212 | |||
chr8:143930221 | G | A | 1 | a0031c0172 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.2493C>T | p.Ser831Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 21/32 | 2550/14683 | 2493/13602 | 831/4533 | chr8 | 143930221 | |||
chr8:143931621 | C | T | 3 | a0037c0079 a0065c0070 a0093c0078 |
3 | HG01109.hp1 HG02922.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.2175G>A | p.Gln725Gln | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/32 | 2232/14683 | 2175/13602 | 725/4533 | chr8 | 143931621 | |||
chr8:143932698 | G | A | 3 | a0004c0178 a0054c0176 a0066c0177 |
3 | HG02258.hp2 HG02818.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.1710C>T | p.Pro570Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 15/32 | 1767/14683 | 1710/13602 | 570/4533 | chr8 | 143932698 | |||
chr8:143933220 | C | T | 1 | a0007c0075 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1353G>A | p.Pro451Pro | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 13/32 | 1410/14683 | 1353/13602 | 451/4533 | chr8 | 143933220 | |||
chr8:143933241 | G | A | 4 | a0004c0175 a0004c0178 a0054c0176 others(1): Show |
4 | HG02258.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.1332C>T | p.Thr444Thr | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 13/32 | 1389/14683 | 1332/13602 | 444/4533 | chr8 | 143933241 | |||
chr8:143934025 | C | T | 2 | a0004c0073 a0004c0074 |
2 | HG01891.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.1194G>A | p.Leu398Leu | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/32 | 1251/14683 | 1194/13602 | 398/4533 | chr8 | 143934025 | |||
chr8:143934392 | A | G | 39 | a0002c0002 a0002c0005 a0002c0019 others(36): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
synonymous_variant | LOW | c.1053T>C | p.Asp351Asp | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 11/32 | 1110/14683 | 1053/13602 | 351/4533 | chr8 | 143934392 | |||
chr8:143934437 | C | T | 1 | a0001c0072 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1008G>A | p.Val336Val | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 11/32 | 1065/14683 | 1008/13602 | 336/4533 | chr8 | 143934437 | |||
chr8:143935985 | C | T | 1 | a0001c0069 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.423G>A | p.Ser141Ser | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 6/32 | 480/14683 | 423/13602 | 141/4533 | chr8 | 143935985 | |||
chr8:143937036 | A | G | 39 | a0002c0002 a0002c0005 a0002c0019 others(36): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
synonymous_variant | LOW | c.336T>C | p.Ala112Ala | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/32 | 393/14683 | 336/13602 | 112/4533 | chr8 | 143937036 | |||
chr8:143938670 | C | T | 1 | a0002c0037 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.93G>A | p.Lys31Lys | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 2/32 | 150/14683 | 93/13602 | 31/4533 | chr8 | 143938670 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143915222 | C | T | 3 | a0002c0019t0007 a0002c0046t0007 a0002c0060t0007 |
4 | NA18952.hp2 NA18984.hp1 NA19067.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*955G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 955 | chr8 | 143915222 | ||||||
chr8:143915294 | A | G | 91 | a0001c0131t0002 a0002c0002t0002 a0002c0005t0002 others(88): Show |
148 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*883T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 883 | chr8 | 143915294 | ||||||
chr8:143915298 | G | A | 1 | a0049c0120t0011 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 879 | chr8 | 143915298 | ||||||
chr8:143915423 | G | A | 1 | a0004c0008t0012 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 754 | chr8 | 143915423 | ||||||
chr8:143915750 | G | A | 6 | a0007c0016t0006 a0007c0075t0006 a0058c0163t0006 others(3): Show |
8 | HG02486.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*427C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 427 | chr8 | 143915750 | ||||||
chr8:143915836 | C | G | 1 | a0001c0001t0010 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 341 | chr8 | 143915836 | ||||||
chr8:143915865 | AC | A | 10 | a0009c0007t0005 a0010c0022t0005 a0010c0083t0005 others(7): Show |
15 | HG01109.hp1 HG01175.hp1 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*311delG | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 311 | chr8 | 143915865 | ||||||
chr8:143915891 | G | A | 2 | a0004c0073t0008 a0004c0074t0008 |
2 | HG01891.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*286C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 286 | chr8 | 143915891 | ||||||
chr8:143916024 | C | T | 1 | a0006c0151t0009 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*153G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 153 | chr8 | 143916024 | ||||||
chr8:143916158 | G | A | 9 | a0005c0003t0004 a0005c0094t0004 a0005c0095t0004 others(6): Show |
18 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*19C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 19 | chr8 | 143916158 | ||||||
chr8:143916167 | G | A | 39 | a0001c0131t0002 a0002c0002t0002 a0002c0002t0013 others(36): Show |
73 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*10C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 32/32 | 10 | chr8 | 143916167 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143922430 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.7384-35C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/31 | chr8 | 143922430 | |||||||
chr8:143922467 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.7383+37C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/31 | chr8 | 143922467 | |||||||
chr8:143922498 | C | CG | 3 | a0001c0013t0001g0175 a0003c0004t0001g0216 a0006c0150t0002g0231 |
3 | HG01928.hp2 NA18977.hp2 NA18982.hp1 |
splice_region_variant&intron_variant | LOW | c.7383+5dupC | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 31/31 | chr8 | 143922498 | |||||||
chr8:143925888 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
splice_region_variant&intron_variant | LOW | c.4003-4A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143925888 | |||||||
chr8:143925994 | G | A | 1 | a0037c0079t0005g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4003-110C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143925994 | |||||||
chr8:143926031 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4003-147G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926031 | |||||||
chr8:143926053 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.4003-169C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926053 | |||||||
chr8:143926137 | G | A | 1 | a0001c0069t0001g0228 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4003-253C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926137 | |||||||
chr8:143926139 | C | T | 2 | a0033c0066t0002g0172 a0034c0101t0002g0159 |
2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.4003-255G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926139 | |||||||
chr8:143926153 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.4003-269G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926153 | |||||||
chr8:143926156 | G | C | 1 | a0013c0010t0002g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4003-272C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926156 | |||||||
chr8:143926190 | C | T | 5 | a0002c0002t0002g0058 a0002c0002t0002g0070 a0002c0002t0002g0073 others(2): Show |
5 | NA18994.hp1 NA19011.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.4003-306G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926190 | |||||||
chr8:143926245 | G | A | 2 | a0033c0066t0002g0172 a0034c0101t0002g0159 |
2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.4003-361C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926245 | |||||||
chr8:143926434 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.4002+350A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926434 | |||||||
chr8:143926470 | G | A | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4002+314C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926470 | |||||||
chr8:143926489 | G | A | 2 | a0065c0070t0003g0013 a0093c0078t0003g0146 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4002+295C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926489 | |||||||
chr8:143926554 | G | A | 1 | a0011c0089t0003g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4002+230C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926554 | |||||||
chr8:143926572 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.4002+212C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926572 | |||||||
chr8:143926598 | G | A | 2 | a0001c0024t0001g0180 a0001c0024t0001g0276 |
2 | NA18962.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.4002+186C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926598 | |||||||
chr8:143926641 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.4002+143C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926641 | |||||||
chr8:143926722 | T | C | 11 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(8): Show |
11 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.4002+62A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926722 | |||||||
chr8:143926730 | A | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.4002+54T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926730 | |||||||
chr8:143926755 | C | T | 1 | a0003c0114t0001g0168 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4002+29G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 30/31 | chr8 | 143926755 | |||||||
chr8:143927099 | G | A | 23 | a0002c0002t0002g0017 a0002c0002t0002g0020 a0002c0002t0002g0028 others(20): Show |
23 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.3799-18C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/31 | chr8 | 143927099 | |||||||
chr8:143927132 | T | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.3799-51A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/31 | chr8 | 143927132 | |||||||
chr8:143927138 | G | A | 21 | a0004c0008t0003g0150 a0004c0008t0003g0240 a0004c0008t0003g0255 others(18): Show |
21 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.3799-57C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/31 | chr8 | 143927138 | |||||||
chr8:143927143 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.3799-62A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/31 | chr8 | 143927143 | |||||||
chr8:143927204 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.3798+48A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 28/31 | chr8 | 143927204 | |||||||
chr8:143927341 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
splice_region_variant&intron_variant | LOW | c.3715-6A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/31 | chr8 | 143927341 | |||||||
chr8:143927344 | T | C | 51 | a0004c0008t0003g0150 a0004c0008t0003g0240 a0004c0008t0003g0255 others(48): Show |
51 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(48): Show |
intron_variant | MODIFIER | c.3715-9A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/31 | chr8 | 143927344 | |||||||
chr8:143927365 | C | T | 2 | a0001c0001t0001g0202 a0002c0019t0007g0038 |
2 | NA18970.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.3715-30G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/31 | chr8 | 143927365 | |||||||
chr8:143927387 | C | T | 1 | a0001c0036t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3714+23G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 27/31 | chr8 | 143927387 | |||||||
chr8:143927792 | C | T | 3 | a0001c0006t0001g0277 a0002c0041t0002g0060 a0036c0057t0002g0024 |
3 | HG01081.hp2 HG01993.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3358-26G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 26/31 | chr8 | 143927792 | |||||||
chr8:143927808 | C | T | 14 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3358-42G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 26/31 | chr8 | 143927808 | |||||||
chr8:143928005 | C | T | 26 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(23): Show |
26 | HG02280.hp2 HG02300.hp1 HG02622.hp1 others(23): Show |
intron_variant | MODIFIER | c.3219-13G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928005 | |||||||
chr8:143928039 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3219-47A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928039 | |||||||
chr8:143928109 | G | T | 1 | a0002c0002t0002g0028 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3219-117C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928109 | |||||||
chr8:143928115 | A | G | 151 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(148): Show |
151 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.3219-123T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928115 | |||||||
chr8:143928210 | A | C | 4 | a0012c0015t0001g0160 a0012c0015t0001g0182 a0012c0015t0001g0198 others(1): Show |
4 | HG00423.hp2 HG00438.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.3219-218T>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928210 | |||||||
chr8:143928227 | C | T | 3 | a0005c0167t0001g0009 a0011c0169t0001g0010 a0079c0168t0001g0012 |
3 | HG02976.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3219-235G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928227 | |||||||
chr8:143928263 | C | G | 72 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3219-271G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928263 | |||||||
chr8:143928321 | C | T | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3219-329G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928321 | |||||||
chr8:143928368 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.3219-376C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928368 | |||||||
chr8:143928395 | A | AGCGGCGG others(601): Show |
1 | a0093c0078t0003g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3219-404_3219-403i others(610): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928395 | |||||||
chr8:143928395 | A | AGCGGCGG others(69): Show |
1 | a0059c0103t0006g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3219-479_3219-404d others(78): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928395 | |||||||
chr8:143928395 | A | AGCGGCGG others(525): Show |
1 | a0064c0087t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3219-404_3219-403i others(534): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928395 | |||||||
chr8:143928395 | A | AGCGGCGG others(448): Show |
1 | a0076c0038t0002g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3219-404_3219-403i others(457): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928395 | |||||||
chr8:143928395 | A | AGCGGCGG others(296): Show |
9 | a0002c0002t0002g0020 a0002c0002t0002g0035 a0002c0019t0007g0038 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.3219-404_3219-403i others(305): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928395 | |||||||
chr8:143928395 | A | AGCGGCGG others(220): Show |
1 | a0002c0002t0002g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3219-404_3219-403i others(229): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928395 | |||||||
chr8:143928395 | A | AGCGGCGG others(294): Show |
1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3219-404_3219-403i others(303): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928395 | |||||||
chr8:143928397 | C | CGGCGGCC others(145): Show |
2 | a0039c0111t0003g0144 a0077c0142t0001g0266 |
2 | HG01346.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3218+554_3219-406d others(154): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928397 | |||||||
chr8:143928397 | CGGCGGCC others(145): Show |
C | 4 | a0001c0036t0001g0220 a0003c0148t0001g0279 a0017c0052t0002g0113 others(1): Show |
4 | HG00323.hp1 HG00639.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3218+554_3219-406d others(2): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928397 | |||||||
chr8:143928398 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3219-406C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928398 | |||||||
chr8:143928400 | C | T | 1 | a0001c0104t0001g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3219-408G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928400 | |||||||
chr8:143928407 | A | G | 1 | a0002c0002t0002g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3219-415T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928407 | |||||||
chr8:143928411 | C | CTGTGCTG others(296): Show |
8 | a0002c0005t0002g0041 a0002c0005t0002g0042 a0002c0005t0002g0050 others(5): Show |
8 | HG00597.hp1 HG02056.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.3219-420_3219-419i others(305): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928411 | |||||||
chr8:143928414 | T | C | 1 | a0048c0092t0001g0284 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3219-422A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928414 | |||||||
chr8:143928424 | G | A | 1 | a0006c0034t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3219-432C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928424 | |||||||
chr8:143928473 | C | T | 4 | a0005c0167t0001g0009 a0011c0169t0001g0010 a0060c0159t0001g0118 others(1): Show |
4 | HG02717.hp1 HG02976.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3219-481G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928473 | |||||||
chr8:143928549 | T | C | 146 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(143): Show |
146 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.3218+554A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928549 | |||||||
chr8:143928549 | TGGCGGCC others(69): Show |
T | 1 | a0049c0120t0011g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3218+478_3218+553d others(78): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928549 | |||||||
chr8:143928588 | C | CAGCGGGT others(601): Show |
1 | a0004c0008t0012g0082 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3218+514_3218+515i others(610): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928588 | |||||||
chr8:143928588 | C | CAGCGGGT others(69): Show |
3 | a0004c0008t0003g0289 a0011c0088t0003g0290 a0011c0089t0003g0288 |
3 | HG02257.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3218+514_3218+515i others(78): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928588 | |||||||
chr8:143928625 | C | CGGCGGCC others(69): Show |
3 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 |
3 | HG02280.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3218+477_3218+478i others(78): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928625 | |||||||
chr8:143928625 | C | T | 6 | a0005c0167t0001g0009 a0007c0016t0006g0087 a0011c0169t0001g0010 others(3): Show |
6 | HG02486.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3218+478G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928625 | |||||||
chr8:143928628 | C | T | 2 | a0004c0086t0003g0217 a0004c0175t0003g0287 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3218+475G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928628 | |||||||
chr8:143928664 | C | CAGCGGGT others(677): Show |
1 | a0004c0175t0003g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3218+438_3218+439i others(686): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(753): Show |
1 | a0004c0086t0003g0217 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3218+438_3218+439i others(762): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(677): Show |
3 | a0004c0178t0003g0138 a0054c0176t0003g0139 a0066c0177t0003g0140 |
3 | HG02258.hp2 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3218+438_3218+439i others(686): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(753): Show |
1 | a0004c0090t0003g0153 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3218+438_3218+439i others(762): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(525): Show |
2 | a0007c0035t0003g0099 a0072c0158t0004g0007 |
2 | HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3218+438_3218+439i others(534): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(525): Show |
2 | a0024c0023t0003g0152 a0024c0023t0003g0212 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3218+438_3218+439i others(534): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(601): Show |
4 | a0004c0008t0003g0150 a0004c0073t0008g0141 a0004c0074t0008g0142 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3218+438_3218+439i others(610): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(677): Show |
1 | a0043c0091t0003g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3218+438_3218+439i others(686): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(449): Show |
3 | a0007c0035t0003g0103 a0011c0156t0003g0105 a0071c0160t0003g0100 |
3 | HG02055.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3218+438_3218+439i others(458): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(373): Show |
3 | a0025c0020t0003g0092 a0025c0020t0003g0093 a0053c0067t0003g0091 |
3 | HG02145.hp1 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3218+438_3218+439i others(382): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(525): Show |
3 | a0004c0008t0003g0240 a0004c0008t0003g0255 a0044c0173t0003g0213 |
3 | HG01884.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3218+438_3218+439i others(534): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(297): Show |
7 | a0002c0002t0002g0045 a0002c0002t0002g0058 a0002c0002t0002g0061 others(4): Show |
7 | NA18982.hp2 NA18994.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.3218+438_3218+439i others(306): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(221): Show |
27 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(24): Show |
27 | HG02145.hp2 HG02258.hp1 HG02300.hp1 others(24): Show |
intron_variant | MODIFIER | c.3218+438_3218+439i others(230): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(601): Show |
1 | a0065c0070t0003g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3218+438_3218+439i others(610): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(145): Show |
1 | a0040c0061t0002g0109 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3218+438_3218+439i others(154): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(296): Show |
1 | a0017c0042t0002g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3218+438_3218+439i others(305): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(145): Show |
8 | a0007c0016t0006g0295 a0010c0022t0005g0011 a0010c0022t0005g0294 others(5): Show |
8 | HG01175.hp1 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3218+438_3218+439i others(154): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(372): Show |
34 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0028 others(31): Show |
34 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.3218+438_3218+439i others(381): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(448): Show |
1 | a0002c0002t0002g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3218+438_3218+439i others(457): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(296): Show |
7 | a0002c0002t0002g0108 a0002c0002t0002g0111 a0002c0002t0002g0114 others(4): Show |
7 | HG01261.hp2 HG01943.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3218+438_3218+439i others(305): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | CAGCGGGT others(220): Show |
1 | a0002c0002t0002g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3218+438_3218+439i others(229): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928664 | C | T | 22 | a0002c0002t0002g0020 a0002c0002t0002g0035 a0002c0002t0002g0036 others(19): Show |
22 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3218+439G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928664 | |||||||
chr8:143928675 | C | CCTGTGGT others(221): Show |
2 | a0009c0007t0005g0076 a0067c0157t0005g0078 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3218+427_3218+428i others(230): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928675 | |||||||
chr8:143928699 | G | A | 1 | a0047c0143t0001g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3218+404C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928699 | |||||||
chr8:143928704 | T | C | 14 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3218+399A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928704 | |||||||
chr8:143928708 | A | G | 1 | a0006c0153t0001g0158 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3218+395T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928708 | |||||||
chr8:143928766 | C | T | 1 | a0003c0110t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3218+337G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928766 | |||||||
chr8:143928779 | G | A | 47 | a0004c0008t0003g0150 a0004c0008t0003g0240 a0004c0008t0003g0255 others(44): Show |
47 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.3218+324C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928779 | |||||||
chr8:143928937 | C | T | 1 | a0083c0130t0001g0251 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3218+166G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143928937 | |||||||
chr8:143929057 | C | A | 4 | a0007c0035t0003g0099 a0007c0035t0003g0103 a0011c0156t0003g0105 others(1): Show |
4 | HG02055.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3218+46G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 25/31 | chr8 | 143929057 | |||||||
chr8:143929401 | G | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0208 |
2 | NA18970.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3039+13C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 24/31 | chr8 | 143929401 | |||||||
chr8:143929609 | G | A | 72 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2881+37C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 23/31 | chr8 | 143929609 | |||||||
chr8:143929858 | G | A | 1 | a0002c0002t0013g0117 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2698-29C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 22/31 | chr8 | 143929858 | |||||||
chr8:143929874 | C | A | 79 | a0004c0008t0003g0150 a0004c0008t0003g0240 a0004c0008t0003g0255 others(76): Show |
79 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.2698-45G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 22/31 | chr8 | 143929874 | |||||||
chr8:143930066 | G | A | 2 | a0037c0079t0005g0115 a0056c0071t0005g0214 |
2 | HG01109.hp1 HG02559.hp1 |
splice_region_variant&intron_variant | LOW | c.2571-4C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 21/31 | chr8 | 143930066 | |||||||
chr8:143930069 | G | T | 18 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(15): Show |
18 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.2571-7C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 21/31 | chr8 | 143930069 | |||||||
chr8:143930378 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0164 a0001c0001t0001g0174 others(159): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
splice_region_variant&intron_variant | LOW | c.2415+6C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 20/31 | chr8 | 143930378 | |||||||
chr8:143930545 | GA | G | 4 | a0004c0175t0003g0287 a0004c0178t0003g0138 a0054c0176t0003g0139 others(1): Show |
4 | HG02258.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2263-10delT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143930545 | |||||||
chr8:143930692 | G | A | 4 | a0004c0175t0003g0287 a0004c0178t0003g0138 a0054c0176t0003g0139 others(1): Show |
4 | HG02258.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2263-156C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143930692 | |||||||
chr8:143930751 | T | G | 1 | a0005c0003t0004g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2263-215A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143930751 | |||||||
chr8:143930776 | T | C | 130 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(127): Show |
130 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.2263-240A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143930776 | |||||||
chr8:143930908 | G | A | 9 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2263-372C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143930908 | |||||||
chr8:143930942 | G | T | 1 | a0002c0002t0002g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2263-406C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143930942 | |||||||
chr8:143931061 | G | A | 27 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(24): Show |
27 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.2262+473C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931061 | |||||||
chr8:143931226 | G | A | 1 | a0002c0065t0002g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2262+308C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931226 | |||||||
chr8:143931273 | T | C | 28 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(25): Show |
28 | HG01175.hp1 HG01192.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.2262+261A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931273 | |||||||
chr8:143931280 | CTTGGCTG others(106): Show |
C | 75 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2262+141_2262+253d others(2): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931280 | |||||||
chr8:143931282 | T | TGGCTGAC others(106): Show |
13 | a0009c0007t0005g0076 a0009c0007t0005g0079 a0009c0007t0005g0080 others(10): Show |
13 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2262+139_2262+251d others(115): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931282 | |||||||
chr8:143931282 | TGGCTGAC others(106): Show |
T | 3 | a0001c0001t0001g0164 a0001c0106t0001g0244 a0001c0171t0001g0239 |
3 | HG00423.hp1 HG02300.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2262+139_2262+251d others(2): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931282 | |||||||
chr8:143931335 | G | A | 4 | a0003c0004t0001g0004 a0003c0004t0001g0216 a0003c0004t0001g0297 others(1): Show |
5 | HG00639.hp2 HG01074.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.2262+199C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931335 | |||||||
chr8:143931509 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2262+25G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931509 | |||||||
chr8:143931520 | A | AC | 88 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(85): Show |
88 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.2262+13dupG | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 19/31 | chr8 | 143931520 | |||||||
chr8:143931928 | G | C | 15 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(12): Show |
15 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2136+9C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 18/31 | chr8 | 143931928 | |||||||
chr8:143932052 | G | A | 1 | a0023c0135t0001g0232 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2041-20C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 17/31 | chr8 | 143932052 | |||||||
chr8:143932057 | G | GGCCCC | 8 | a0009c0007t0005g0076 a0009c0007t0005g0079 a0009c0007t0005g0080 others(5): Show |
8 | HG01192.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041-30_2041-26dup others(5): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 17/31 | chr8 | 143932057 | |||||||
chr8:143932058 | G | GCCCCA | 5 | a0010c0022t0005g0011 a0010c0022t0005g0294 a0010c0083t0005g0293 others(2): Show |
5 | HG01175.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041-27_2041-26ins others(5): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 17/31 | chr8 | 143932058 | |||||||
chr8:143932277 | C | T | 1 | a0052c0174t0003g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1936-43G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 16/31 | chr8 | 143932277 | |||||||
chr8:143932580 | G | A | 1 | a0001c0009t0001g0296 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1774-19C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 15/31 | chr8 | 143932580 | |||||||
chr8:143932592 | C | T | 1 | a0001c0149t0001g0242 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1774-31G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 15/31 | chr8 | 143932592 | |||||||
chr8:143932612 | C | T | 1 | a0070c0093t0004g0129 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1773+23G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 15/31 | chr8 | 143932612 | |||||||
chr8:143932622 | T | C | 106 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(103): Show |
106 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1773+13A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 15/31 | chr8 | 143932622 | |||||||
chr8:143932625 | C | T | 1 | a0001c0069t0001g0228 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1773+10G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 15/31 | chr8 | 143932625 | |||||||
chr8:143933157 | G | A | 17 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(14): Show |
17 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1376+40C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 13/31 | chr8 | 143933157 | |||||||
chr8:143933366 | C | T | 132 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(129): Show |
132 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.1222-15G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933366 | |||||||
chr8:143933712 | T | C | 1 | a0002c0051t0002g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1221+286A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933712 | |||||||
chr8:143933779 | G | A | 72 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1221+219C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933779 | |||||||
chr8:143933821 | A | G | 76 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1221+177T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933821 | |||||||
chr8:143933844 | C | T | 1 | a0052c0174t0003g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1221+154G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933844 | |||||||
chr8:143933918 | C | G | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1221+80G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933918 | |||||||
chr8:143933943 | G | A | 2 | a0005c0003t0004g0126 a0005c0003t0004g0127 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1221+55C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933943 | |||||||
chr8:143933947 | C | G | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1221+51G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933947 | |||||||
chr8:143933948 | A | G | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1221+50T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933948 | |||||||
chr8:143933955 | T | G | 1 | a0002c0047t0002g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1221+43A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933955 | |||||||
chr8:143933957 | C | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1221+41G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933957 | |||||||
chr8:143933961 | C | G | 1 | a0012c0015t0001g0160 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1221+37G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933961 | |||||||
chr8:143933987 | C | CCGACTGC others(10): Show |
9 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1221+10_1221+11ins others(17): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933987 | |||||||
chr8:143933990 | C | T | 9 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02723.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1221+8G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933990 | |||||||
chr8:143933991 | C | G | 9 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02723.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1221+7G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 12/31 | chr8 | 143933991 | |||||||
chr8:143934174 | C | A | 71 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(68): Show |
71 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1128-83G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 11/31 | chr8 | 143934174 | |||||||
chr8:143934182 | C | T | 1 | a0002c0005t0002g0055 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1128-91G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 11/31 | chr8 | 143934182 | |||||||
chr8:143934233 | G | A | 2 | a0011c0169t0001g0010 a0079c0168t0001g0012 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1127+85C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 11/31 | chr8 | 143934233 | |||||||
chr8:143934275 | A | T | 76 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1127+43T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 11/31 | chr8 | 143934275 | |||||||
chr8:143934456 | G | A | 1 | a0004c0008t0003g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1000-11C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 10/31 | chr8 | 143934456 | |||||||
chr8:143934516 | C | T | 4 | a0007c0035t0003g0099 a0007c0035t0003g0103 a0011c0156t0003g0105 others(1): Show |
4 | HG02055.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-71G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 10/31 | chr8 | 143934516 | |||||||
chr8:143934538 | C | T | 75 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1000-93G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 10/31 | chr8 | 143934538 | |||||||
chr8:143934763 | G | C | 130 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(127): Show |
130 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.904-33C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 9/31 | chr8 | 143934763 | |||||||
chr8:143934763 | G | T | 2 | a0002c0005t0002g0041 a0002c0005t0002g0055 |
2 | HG00597.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.904-33C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 9/31 | chr8 | 143934763 | |||||||
chr8:143934933 | C | T | 1 | a0006c0150t0002g0231 | 1 | NA18982.hp1 | splice_region_variant&intron_variant | LOW | c.784-4G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 8/31 | chr8 | 143934933 | |||||||
chr8:143934969 | C | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0058c0163t0006g0104 |
3 | HG02572.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.784-40G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 8/31 | chr8 | 143934969 | |||||||
chr8:143935188 | G | A | 9 | a0001c0001t0001g0174 a0001c0001t0001g0227 a0001c0001t0001g0283 others(6): Show |
9 | HG00099.hp1 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+10C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 7/31 | chr8 | 143935188 | |||||||
chr8:143935425 | A | C | 132 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(129): Show |
132 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.561-112T>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 6/31 | chr8 | 143935425 | |||||||
chr8:143935442 | A | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.561-129T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 6/31 | chr8 | 143935442 | |||||||
chr8:143935523 | G | A | 2 | a0001c0024t0001g0180 a0001c0024t0001g0276 |
2 | NA18962.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.561-210C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 6/31 | chr8 | 143935523 | |||||||
chr8:143935718 | G | A | 12 | a0009c0007t0005g0076 a0009c0007t0005g0079 a0009c0007t0005g0080 others(9): Show |
12 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.560+130C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 6/31 | chr8 | 143935718 | |||||||
chr8:143935836 | G | A | 2 | a0043c0091t0003g0006 a0072c0158t0004g0007 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.560+12C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 6/31 | chr8 | 143935836 | |||||||
chr8:143936137 | A | G | 99 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(96): Show |
99 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.394-123T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936137 | |||||||
chr8:143936144 | A | G | 1 | a0006c0034t0001g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.394-130T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936144 | |||||||
chr8:143936155 | G | A | 4 | a0037c0079t0005g0115 a0052c0174t0003g0097 a0065c0070t0003g0013 others(1): Show |
4 | HG01109.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-141C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936155 | |||||||
chr8:143936167 | C | T | 12 | a0009c0007t0005g0076 a0009c0007t0005g0079 a0009c0007t0005g0080 others(9): Show |
12 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-153G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936167 | |||||||
chr8:143936177 | T | C | 33 | a0005c0167t0001g0009 a0007c0016t0006g0086 a0007c0016t0006g0087 others(30): Show |
33 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.394-163A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936177 | |||||||
chr8:143936312 | G | A | 4 | a0037c0079t0005g0115 a0052c0174t0003g0097 a0065c0070t0003g0013 others(1): Show |
4 | HG01109.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-298C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936312 | |||||||
chr8:143936346 | T | C | 132 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(129): Show |
132 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.394-332A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936346 | |||||||
chr8:143936584 | C | T | 75 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.393+395G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936584 | |||||||
chr8:143936601 | C | G | 2 | a0002c0002t0002g0108 a0002c0002t0002g0111 |
2 | HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.393+378G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936601 | |||||||
chr8:143936658 | G | T | 2 | a0002c0041t0002g0060 a0036c0057t0002g0024 |
2 | HG01081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.393+321C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936658 | |||||||
chr8:143936889 | C | G | 2 | a0005c0167t0001g0009 a0010c0022t0005g0011 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.393+90G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 5/31 | chr8 | 143936889 | |||||||
chr8:143937152 | C | T | 4 | a0037c0079t0005g0115 a0052c0174t0003g0097 a0065c0070t0003g0013 others(1): Show |
4 | HG01109.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+13G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 4/31 | chr8 | 143937152 | |||||||
chr8:143937258 | G | C | 20 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(17): Show |
20 | HG02280.hp2 HG02300.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.223-16C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 3/31 | chr8 | 143937258 | |||||||
chr8:143937458 | C | G | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.223-216G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 3/31 | chr8 | 143937458 | |||||||
chr8:143937901 | G | A | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.222+250C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 3/31 | chr8 | 143937901 | |||||||
chr8:143938003 | G | A | 3 | a0037c0079t0005g0115 a0065c0070t0003g0013 a0093c0078t0003g0146 |
3 | HG01109.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.222+148C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 3/31 | chr8 | 143938003 | |||||||
chr8:143938038 | G | A | 99 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(96): Show |
99 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.222+113C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 3/31 | chr8 | 143938038 | |||||||
chr8:143938136 | C | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.222+15G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 3/31 | chr8 | 143938136 | |||||||
chr8:143938246 | G | A | 2 | a0005c0003t0004g0126 a0005c0003t0004g0127 |
2 | HG02630.hp2 HG02717.hp2 |
splice_region_variant&intron_variant | LOW | c.133-6C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 2/31 | chr8 | 143938246 | |||||||
chr8:143938298 | A | G | 75 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.133-58T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 2/31 | chr8 | 143938298 | |||||||
chr8:143938474 | G | A | 1 | a0068c0138t0005g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132+157C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 2/31 | chr8 | 143938474 | |||||||
chr8:143938581 | G | A | 55 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(52): Show |
55 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.132+50C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 2/31 | chr8 | 143938581 | |||||||
chr8:143938609 | C | G | 70 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(67): Show |
70 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.132+22G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 2/31 | chr8 | 143938609 | |||||||
chr8:143938609 | C | T | 23 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(20): Show |
23 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.132+22G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 2/31 | chr8 | 143938609 | |||||||
chr8:143938738 | G | A | 5 | a0007c0035t0003g0099 a0007c0035t0003g0103 a0043c0091t0003g0006 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-46C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143938738 | |||||||
chr8:143938808 | A | G | 1 | a0011c0089t0003g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71-116T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143938808 | |||||||
chr8:143938996 | T | TC | 72 | a0001c0001t0001g0207 a0002c0002t0002g0015 a0002c0002t0002g0017 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.71-305dupG | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143938996 | |||||||
chr8:143939147 | G | T | 77 | a0001c0001t0001g0257 a0002c0002t0002g0015 a0002c0002t0002g0017 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.71-455C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939147 | |||||||
chr8:143939177 | C | T | 76 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.71-485G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939177 | |||||||
chr8:143939202 | C | T | 1 | a0007c0035t0003g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.71-510G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939202 | |||||||
chr8:143939607 | G | A | 1 | a0002c0002t0002g0031 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.71-915C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939607 | |||||||
chr8:143939725 | C | G | 76 | a0001c0001t0001g0272 a0002c0002t0002g0015 a0002c0002t0002g0017 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.71-1033G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939725 | |||||||
chr8:143939780 | A | ACCCCGAC others(38): Show |
1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.71-1133_71-1089dup others(45): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939780 | |||||||
chr8:143939781 | C | T | 76 | a0001c0131t0002g0163 a0002c0002t0002g0015 a0002c0002t0002g0017 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.71-1089G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939781 | |||||||
chr8:143939785 | G | A | 1 | a0002c0002t0002g0035 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.71-1093C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939785 | |||||||
chr8:143939819 | C | CAG | 75 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.71-1128_71-1127ins others(2): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143939819 | |||||||
chr8:143940026 | G | A | 1 | a0052c0174t0003g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71-1334C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940026 | |||||||
chr8:143940044 | T | G | 1 | a0002c0060t0007g0048 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.71-1352A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940044 | |||||||
chr8:143940119 | T | C | 2 | a0015c0027t0001g0243 a0015c0107t0001g0157 |
2 | HG02080.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.71-1427A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940119 | |||||||
chr8:143940256 | C | G | 69 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(66): Show |
69 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.71-1564G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940256 | |||||||
chr8:143940313 | G | A | 1 | a0050c0170t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.71-1621C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940313 | |||||||
chr8:143940416 | C | G | 1 | a0004c0025t0003g0094 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-1724G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940416 | |||||||
chr8:143940481 | C | G | 18 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(15): Show |
18 | HG01884.hp1 HG02300.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.71-1789G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940481 | |||||||
chr8:143940564 | C | T | 75 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.71-1872G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940564 | |||||||
chr8:143940573 | C | G | 1 | a0014c0063t0001g0110 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.71-1881G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940573 | |||||||
chr8:143940760 | A | G | 19 | a0004c0008t0012g0082 a0007c0016t0006g0086 a0007c0016t0006g0087 others(16): Show |
19 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.71-2068T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940760 | |||||||
chr8:143940866 | C | T | 32 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(29): Show |
32 | HG01175.hp1 HG01192.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.71-2174G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940866 | |||||||
chr8:143940876 | C | T | 1 | a0052c0174t0003g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71-2184G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940876 | |||||||
chr8:143940901 | A | G | 1 | a0002c0002t0002g0035 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.71-2209T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940901 | |||||||
chr8:143940982 | G | A | 1 | a0047c0143t0001g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.71-2290C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143940982 | |||||||
chr8:143941145 | T | C | 1 | a0002c0002t0013g0117 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.71-2453A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143941145 | |||||||
chr8:143941189 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0210 a0001c0001t0001g0223 others(10): Show |
15 | HG00438.hp2 HG00673.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-2497C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143941189 | |||||||
chr8:143941686 | G | A | 1 | a0088c0099t0004g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-2994C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143941686 | |||||||
chr8:143941801 | C | A | 1 | a0001c0139t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.71-3109G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143941801 | |||||||
chr8:143941853 | G | A | 1 | a0004c0090t0003g0153 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.71-3161C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143941853 | |||||||
chr8:143941888 | G | A | 1 | a0001c0166t0001g0194 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.71-3196C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143941888 | |||||||
chr8:143942047 | T | C | 5 | a0005c0094t0004g0134 a0016c0012t0004g0132 a0016c0012t0004g0133 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3355A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942047 | |||||||
chr8:143942148 | GCCAGCCC others(8): Show |
G | 12 | a0001c0001t0001g0257 a0002c0002t0002g0058 a0002c0002t0002g0070 others(9): Show |
12 | HG01884.hp1 HG01975.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-3471_71-3457del others(15): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942148 | |||||||
chr8:143942200 | A | G | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-3508T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942200 | |||||||
chr8:143942207 | G | A | 1 | a0002c0019t0007g0049 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.71-3515C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942207 | |||||||
chr8:143942220 | C | T | 1 | a0059c0103t0006g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.71-3528G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942220 | |||||||
chr8:143942330 | GCCCCACT others(64): Show |
G | 1 | a0037c0079t0005g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71-3709_71-3639del others(71): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942330 | |||||||
chr8:143942402 | C | G | 1 | a0037c0079t0005g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71-3710G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942402 | |||||||
chr8:143942403 | A | T | 1 | a0037c0079t0005g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71-3711T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942403 | |||||||
chr8:143942489 | G | C | 1 | a0002c0047t0002g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-3797C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942489 | |||||||
chr8:143942573 | G | A | 1 | a0005c0094t0004g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.71-3881C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942573 | |||||||
chr8:143942642 | C | G | 1 | a0001c0028t0001g0267 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.71-3950G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942642 | |||||||
chr8:143942649 | T | C | 1 | a0006c0153t0001g0158 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.71-3957A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942649 | |||||||
chr8:143942655 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.71-3963G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942655 | |||||||
chr8:143942712 | A | C | 1 | a0001c0112t0001g0273 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.71-4020T>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942712 | |||||||
chr8:143942748 | G | C | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-4056C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942748 | |||||||
chr8:143942850 | G | A | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71-4158C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942850 | |||||||
chr8:143942961 | A | G | 1 | a0034c0101t0002g0159 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.71-4269T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143942961 | |||||||
chr8:143943116 | C | T | 3 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 |
3 | HG02280.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71-4424G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143943116 | |||||||
chr8:143943419 | T | C | 2 | a0043c0091t0003g0006 a0072c0158t0004g0007 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.71-4727A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143943419 | |||||||
chr8:143943719 | G | A | 3 | a0001c0001t0001g0219 a0001c0036t0001g0220 a0001c0036t0001g0221 |
3 | HG00140.hp1 HG00280.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.71-5027C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143943719 | |||||||
chr8:143943769 | C | A | 2 | a0005c0167t0001g0009 a0010c0022t0005g0011 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.71-5077G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143943769 | |||||||
chr8:143943970 | G | A | 1 | a0001c0001t0010g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.71-5278C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143943970 | |||||||
chr8:143944039 | C | T | 1 | a0002c0065t0002g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.71-5347G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944039 | |||||||
chr8:143944186 | C | T | 2 | a0002c0002t0002g0031 a0002c0053t0002g0068 |
2 | HG01517.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.71-5494G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944186 | |||||||
chr8:143944200 | C | T | 1 | a0068c0138t0005g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-5508G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944200 | |||||||
chr8:143944228 | GCCGCACG others(17): Show |
G | 1 | a0003c0148t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.71-5560_71-5537del others(24): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944228 | |||||||
chr8:143944231 | G | C | 1 | a0001c0009t0001g0252 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.71-5539C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944231 | |||||||
chr8:143944358 | G | A | 1 | a0037c0079t0005g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71-5666C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944358 | |||||||
chr8:143944495 | G | C | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71-5803C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944495 | |||||||
chr8:143944572 | T | TCAGCCC | 15 | a0001c0001t0001g0003 a0001c0001t0001g0210 a0001c0001t0001g0223 others(12): Show |
17 | HG00438.hp2 HG00673.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-5886_71-5881dup others(6): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944572 | |||||||
chr8:143944649 | G | A | 1 | a0002c0002t0002g0031 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.71-5957C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944649 | |||||||
chr8:143944724 | A | G | 1 | a0051c0117t0001g0199 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.71-6032T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944724 | |||||||
chr8:143944909 | C | A | 34 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(31): Show |
34 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-6217G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944909 | |||||||
chr8:143944923 | C | G | 8 | a0001c0006t0001g0145 a0001c0006t0001g0235 a0001c0006t0001g0237 others(5): Show |
8 | HG01123.hp2 HG01358.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-6231G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143944923 | |||||||
chr8:143945014 | G | A | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71-6322C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945014 | |||||||
chr8:143945022 | C | CGGGCTCA others(18): Show |
12 | a0005c0167t0001g0009 a0007c0035t0003g0099 a0007c0035t0003g0103 others(9): Show |
12 | HG01884.hp1 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-6355_71-6331dup others(25): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945022 | |||||||
chr8:143945022 | C | CGGGCTCA others(43): Show |
2 | a0011c0169t0001g0010 a0079c0168t0001g0012 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.71-6331_71-6330ins others(50): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945022 | |||||||
chr8:143945030 | C | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-6338G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945030 | |||||||
chr8:143945353 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.71-6661T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945353 | |||||||
chr8:143945438 | C | T | 1 | a0008c0055t0002g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.71-6746G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945438 | |||||||
chr8:143945448 | C | T | 6 | a0001c0001t0001g0174 a0001c0001t0001g0227 a0001c0001t0001g0283 others(3): Show |
6 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-6756G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945448 | |||||||
chr8:143945570 | G | A | 4 | a0037c0079t0005g0115 a0052c0174t0003g0097 a0065c0070t0003g0013 others(1): Show |
4 | HG01109.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6878C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945570 | |||||||
chr8:143945826 | T | G | 1 | a0003c0114t0001g0168 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.71-7134A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945826 | |||||||
chr8:143945857 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.71-7165C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143945857 | |||||||
chr8:143946154 | GAGGTCCG others(3): Show |
G | 1 | a0003c0105t0001g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71-7472_71-7463del others(10): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946154 | |||||||
chr8:143946174 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.71-7482G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946174 | |||||||
chr8:143946179 | G | A | 3 | a0007c0035t0003g0099 a0007c0035t0003g0103 a0071c0160t0003g0100 |
3 | HG02723.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.71-7487C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946179 | |||||||
chr8:143946308 | C | A | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.71-7616G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946308 | |||||||
chr8:143946309 | T | C | 80 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(77): Show |
80 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.71-7617A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946309 | |||||||
chr8:143946468 | G | A | 76 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.71-7776C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946468 | |||||||
chr8:143946599 | A | G | 3 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 |
3 | HG02280.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71-7907T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946599 | |||||||
chr8:143946669 | G | GCCCCGCC others(9): Show |
3 | a0037c0079t0005g0115 a0065c0070t0003g0013 a0093c0078t0003g0146 |
3 | HG01109.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-7993_71-7978dup others(16): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946669 | |||||||
chr8:143946689 | C | T | 77 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.71-7997G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946689 | |||||||
chr8:143946999 | C | G | 77 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.71-8307G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143946999 | |||||||
chr8:143947067 | C | T | 1 | a0043c0091t0003g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.71-8375G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947067 | |||||||
chr8:143947074 | G | A | 8 | a0007c0035t0003g0099 a0007c0035t0003g0103 a0011c0156t0003g0105 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-8382C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947074 | |||||||
chr8:143947115 | C | T | 1 | a0033c0066t0002g0172 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-8423G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947115 | |||||||
chr8:143947134 | C | T | 3 | a0001c0024t0001g0276 a0001c0031t0001g0179 a0006c0151t0009g0201 |
3 | NA18962.hp1 NA18962.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.71-8442G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947134 | |||||||
chr8:143947260 | G | C | 97 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(94): Show |
97 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.71-8568C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947260 | |||||||
chr8:143947351 | A | G | 1 | a0007c0016t0006g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.71-8659T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947351 | |||||||
chr8:143947403 | T | C | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.71-8711A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947403 | |||||||
chr8:143947404 | C | T | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.71-8712G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947404 | |||||||
chr8:143947519 | C | G | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.71-8827G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947519 | |||||||
chr8:143947520 | G | C | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.71-8828C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947520 | |||||||
chr8:143947582 | T | TA | 10 | a0001c0001t0001g0274 a0002c0002t0002g0061 a0003c0148t0001g0279 others(7): Show |
10 | HG00597.hp2 HG02258.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-8891dupT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947582 | |||||||
chr8:143947675 | G | A | 1 | a0001c0036t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.71-8983C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947675 | |||||||
chr8:143947756 | A | G | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71-9064T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947756 | |||||||
chr8:143947773 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.71-9081C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947773 | |||||||
chr8:143947846 | C | T | 2 | a0002c0041t0002g0060 a0036c0057t0002g0024 |
2 | HG01081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.71-9154G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143947846 | |||||||
chr8:143948088 | C | T | 3 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 |
3 | HG02280.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71-9396G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948088 | |||||||
chr8:143948186 | T | C | 38 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(35): Show |
38 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.71-9494A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948186 | |||||||
chr8:143948186 | T | G | 75 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.71-9494A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948186 | |||||||
chr8:143948378 | C | T | 12 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(9): Show |
12 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-9686G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948378 | |||||||
chr8:143948398 | G | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-9706C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948398 | |||||||
chr8:143948489 | G | T | 136 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(133): Show |
136 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.71-9797C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948489 | |||||||
chr8:143948519 | T | A | 1 | a0002c0002t0002g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.71-9827A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948519 | |||||||
chr8:143948569 | C | A | 1 | a0002c0047t0002g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-9877G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948569 | |||||||
chr8:143948709 | A | C | 31 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(28): Show |
31 | HG01175.hp1 HG01192.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.71-10017T>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948709 | |||||||
chr8:143948709 | A | T | 83 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(80): Show |
83 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.71-10017T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948709 | |||||||
chr8:143948777 | A | G | 1 | a0003c0148t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.71-10085T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948777 | |||||||
chr8:143948779 | G | A | 1 | a0003c0148t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.71-10087C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948779 | |||||||
chr8:143948780 | A | G | 1 | a0003c0148t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.71-10088T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948780 | |||||||
chr8:143948864 | G | A | 1 | a0001c0006t0001g0238 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.71-10172C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948864 | |||||||
chr8:143948869 | C | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-10177G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948869 | |||||||
chr8:143948904 | C | T | 8 | a0007c0035t0003g0099 a0007c0035t0003g0103 a0011c0156t0003g0105 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-10212G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948904 | |||||||
chr8:143948920 | T | A | 32 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(29): Show |
32 | HG01175.hp1 HG01192.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.71-10228A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948920 | |||||||
chr8:143948986 | C | A | 1 | a0004c0008t0003g0255 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.71-10294G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143948986 | |||||||
chr8:143949002 | A | C | 1 | a0002c0002t0002g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.71-10310T>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949002 | |||||||
chr8:143949016 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.71-10324C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949016 | |||||||
chr8:143949094 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0250 a0032c0108t0001g0265 |
3 | HG00597.hp2 HG02015.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.71-10402G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949094 | |||||||
chr8:143949137 | C | T | 1 | a0018c0018t0002g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-10445G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949137 | |||||||
chr8:143949203 | C | T | 2 | a0011c0169t0001g0010 a0079c0168t0001g0012 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.71-10511G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949203 | |||||||
chr8:143949301 | G | T | 1 | a0003c0148t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.71-10609C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949301 | |||||||
chr8:143949302 | T | G | 1 | a0003c0148t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.71-10610A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949302 | |||||||
chr8:143949366 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.71-10674C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949366 | |||||||
chr8:143949516 | C | T | 3 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 |
3 | HG02280.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71-10824G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949516 | |||||||
chr8:143949534 | G | C | 1 | a0036c0057t0002g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.71-10842C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949534 | |||||||
chr8:143949556 | G | C | 31 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(28): Show |
31 | HG01175.hp1 HG01192.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.71-10864C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949556 | |||||||
chr8:143949571 | A | G | 84 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(81): Show |
84 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.71-10879T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949571 | |||||||
chr8:143949652 | G | A | 8 | a0007c0035t0003g0099 a0007c0035t0003g0103 a0011c0156t0003g0105 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-10960C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949652 | |||||||
chr8:143949654 | C | T | 9 | a0002c0002t0002g0017 a0002c0002t0002g0035 a0002c0002t0002g0136 others(6): Show |
9 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-10962G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949654 | |||||||
chr8:143949747 | G | A | 1 | a0034c0101t0002g0159 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.71-11055C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949747 | |||||||
chr8:143949801 | G | A | 1 | a0001c0032t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.71-11109C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949801 | |||||||
chr8:143949862 | T | G | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71-11170A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949862 | |||||||
chr8:143949930 | G | A | 1 | a0003c0110t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.71-11238C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949930 | |||||||
chr8:143949955 | T | G | 11 | a0014c0062t0001g0106 a0025c0020t0003g0092 a0025c0020t0003g0093 others(8): Show |
11 | HG01109.hp1 HG01346.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-11263A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949955 | |||||||
chr8:143949987 | G | A | 1 | a0052c0174t0003g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71-11295C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143949987 | |||||||
chr8:143950043 | G | C | 1 | a0001c0009t0001g0197 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.71-11351C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950043 | |||||||
chr8:143950043 | G | T | 2 | a0002c0002t0002g0061 a0060c0159t0001g0118 |
2 | HG02717.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.71-11351C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950043 | |||||||
chr8:143950062 | T | A | 4 | a0012c0015t0001g0160 a0012c0015t0001g0182 a0012c0015t0001g0198 others(1): Show |
4 | HG00423.hp2 HG00438.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-11370A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950062 | |||||||
chr8:143950167 | G | A | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71-11475C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950167 | |||||||
chr8:143950299 | C | T | 1 | a0001c0104t0001g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.71-11607G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950299 | |||||||
chr8:143950395 | G | A | 2 | a0012c0015t0001g0160 a0012c0015t0001g0182 |
2 | HG00438.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.71-11703C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950395 | |||||||
chr8:143950588 | A | G | 1 | a0047c0143t0001g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.71-11896T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950588 | |||||||
chr8:143950640 | C | T | 1 | a0031c0172t0001g0183 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.71-11948G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950640 | |||||||
chr8:143950650 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.71-11958C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950650 | |||||||
chr8:143950698 | G | A | 1 | a0033c0066t0002g0172 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-12006C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950698 | |||||||
chr8:143950782 | G | A | 1 | a0009c0007t0005g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.71-12090C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950782 | |||||||
chr8:143950892 | G | C | 3 | a0002c0002t0002g0136 a0002c0002t0002g0137 a0041c0048t0002g0025 |
3 | HG01358.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.71-12200C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143950892 | |||||||
chr8:143951049 | G | A | 2 | a0011c0169t0001g0010 a0079c0168t0001g0012 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.71-12357C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951049 | |||||||
chr8:143951130 | C | T | 54 | a0001c0001t0001g0219 a0001c0001t0001g0257 a0001c0009t0001g0296 others(51): Show |
56 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.71-12438G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951130 | |||||||
chr8:143951322 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | NA18747.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.71-12630C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951322 | |||||||
chr8:143951377 | G | T | 1 | a0002c0053t0002g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.71-12685C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951377 | |||||||
chr8:143951479 | C | A | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71-12787G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951479 | |||||||
chr8:143951640 | G | A | 1 | a0003c0004t0001g0224 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.71-12948C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951640 | |||||||
chr8:143951871 | C | G | 2 | a0001c0001t0001g0207 a0060c0159t0001g0118 |
2 | HG02717.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.71-13179G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951871 | |||||||
chr8:143951872 | C | A | 12 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(9): Show |
12 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-13180G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951872 | |||||||
chr8:143951892 | C | T | 5 | a0005c0094t0004g0134 a0016c0012t0004g0132 a0016c0012t0004g0133 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-13200G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143951892 | |||||||
chr8:143952015 | C | T | 1 | a0059c0103t0006g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.71-13323G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952015 | |||||||
chr8:143952026 | C | T | 2 | a0001c0128t0001g0234 a0001c0149t0001g0242 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.71-13334G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952026 | |||||||
chr8:143952072 | G | A | 1 | a0015c0027t0001g0243 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.71-13380C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952072 | |||||||
chr8:143952106 | C | T | 3 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 |
3 | HG02280.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71-13414G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952106 | |||||||
chr8:143952113 | C | A | 1 | a0003c0110t0001g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.71-13421G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952113 | |||||||
chr8:143952179 | CAA | C | 3 | a0004c0008t0003g0289 a0011c0088t0003g0290 a0011c0089t0003g0288 |
3 | HG02257.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.71-13489_71-13488d others(4): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952179 | |||||||
chr8:143952181 | A | AAC | 8 | a0001c0001t0001g0249 a0001c0001t0001g0272 a0001c0001t0001g0275 others(5): Show |
8 | HG02004.hp1 HG02040.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-13491_71-13490d others(4): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952181 | |||||||
chr8:143952181 | A | AACAC | 4 | a0002c0047t0002g0018 a0003c0004t0001g0005 a0004c0008t0012g0082 others(1): Show |
4 | HG01167.hp2 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-13493_71-13490d others(6): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952181 | |||||||
chr8:143952181 | A | AACACACA others(1): Show |
7 | a0001c0028t0001g0267 a0003c0004t0001g0005 a0003c0004t0001g0216 others(4): Show |
7 | HG00642.hp1 HG01168.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-13497_71-13490d others(10): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952181 | |||||||
chr8:143952181 | A | AACACACA others(3): Show |
4 | a0001c0036t0001g0220 a0002c0059t0002g0033 a0003c0004t0001g0004 others(1): Show |
5 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-13499_71-13490d others(12): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952181 | |||||||
chr8:143952181 | AAC | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0164 a0001c0001t0001g0188 others(82): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.71-13491_71-13490d others(4): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952181 | |||||||
chr8:143952181 | AACAC | A | 5 | a0001c0006t0001g0277 a0001c0133t0001g0170 a0003c0148t0001g0279 others(2): Show |
5 | HG00140.hp2 HG01928.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-13493_71-13490d others(6): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952181 | |||||||
chr8:143952206 | ACACG | A | 16 | a0004c0025t0003g0095 a0004c0096t0003g0096 a0005c0003t0004g0014 others(13): Show |
16 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-13518_71-13515d others(6): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952206 | |||||||
chr8:143952206 | ACACGCGC others(1): Show |
A | 4 | a0039c0111t0003g0144 a0064c0087t0003g0077 a0065c0070t0003g0013 others(1): Show |
4 | HG01346.hp1 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-13522_71-13515d others(10): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952206 | |||||||
chr8:143952208 | A | G | 10 | a0001c0001t0001g0263 a0001c0140t0001g0285 a0001c0141t0001g0262 others(7): Show |
10 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-13516T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952208 | |||||||
chr8:143952208 | ACG | A | 25 | a0004c0025t0003g0094 a0005c0003t0004g0124 a0005c0003t0004g0130 others(22): Show |
25 | HG00099.hp2 HG00735.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.71-13518_71-13517d others(4): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952208 | |||||||
chr8:143952210 | G | A | 83 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(80): Show |
83 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.71-13518C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952210 | |||||||
chr8:143952212 | G | A | 101 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(98): Show |
101 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.71-13520C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952212 | |||||||
chr8:143952214 | G | A | 72 | a0001c0069t0001g0228 a0002c0002t0002g0015 a0002c0002t0002g0017 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.71-13522C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952214 | |||||||
chr8:143952216 | A | G | 2 | a0002c0059t0002g0033 a0030c0129t0001g0233 |
2 | HG00408.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.71-13524T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952216 | |||||||
chr8:143952216 | ACACACG | A | 9 | a0004c0008t0003g0150 a0004c0008t0003g0240 a0004c0008t0003g0255 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-13530_71-13525d others(8): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952216 | |||||||
chr8:143952218 | A | ACG | 11 | a0002c0002t0002g0036 a0002c0002t0002g0061 a0002c0002t0002g0136 others(8): Show |
11 | HG01516.hp2 HG01517.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-13527_71-13526i others(4): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952218 | |||||||
chr8:143952218 | A | G | 13 | a0002c0002t0002g0020 a0002c0002t0002g0031 a0002c0002t0002g0053 others(10): Show |
13 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-13526T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952218 | |||||||
chr8:143952220 | A | ACACACAC others(5): Show |
2 | a0002c0053t0002g0068 a0002c0058t0002g0023 |
2 | HG01106.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.71-13529_71-13528i others(14): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952220 | |||||||
chr8:143952220 | A | ACACACAC others(3): Show |
1 | a0018c0018t0002g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-13529_71-13528i others(12): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952220 | |||||||
chr8:143952220 | A | ACACGCG | 16 | a0002c0002t0002g0015 a0002c0002t0002g0028 a0002c0002t0002g0032 others(13): Show |
16 | HG01074.hp2 HG01175.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-13529_71-13528i others(8): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952220 | |||||||
chr8:143952220 | A | ACGCG | 22 | a0002c0002t0002g0017 a0002c0002t0002g0035 a0002c0002t0002g0045 others(19): Show |
22 | HG00597.hp1 HG00621.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.71-13529_71-13528i others(6): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952220 | |||||||
chr8:143952220 | A | G | 30 | a0002c0002t0002g0020 a0002c0002t0002g0031 a0002c0002t0002g0034 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.71-13528T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952220 | |||||||
chr8:143952220 | ACGCACGC others(1): Show |
A | 6 | a0008c0011t0002g0030 a0037c0079t0005g0115 a0039c0111t0003g0144 others(3): Show |
6 | HG01109.hp1 HG01346.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-13536_71-13529d others(10): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952220 | |||||||
chr8:143952263 | C | G | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.71-13571G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952263 | |||||||
chr8:143952264 | G | C | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.71-13572C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952264 | |||||||
chr8:143952282 | T | C | 117 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(114): Show |
117 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.71-13590A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952282 | |||||||
chr8:143952330 | G | T | 1 | a0001c0009t0001g0197 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.71-13638C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952330 | |||||||
chr8:143952405 | G | A | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.71-13713C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952405 | |||||||
chr8:143952414 | G | A | 81 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(78): Show |
81 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.71-13722C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952414 | |||||||
chr8:143952483 | A | C | 1 | a0006c0152t0001g0211 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.71-13791T>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952483 | |||||||
chr8:143952564 | C | A | 1 | a0051c0117t0001g0199 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.71-13872G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952564 | |||||||
chr8:143952728 | T | A | 1 | a0010c0083t0005g0293 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.71-14036A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952728 | |||||||
chr8:143952889 | A | T | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.71-14197T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952889 | |||||||
chr8:143952991 | A | AC | 47 | a0001c0001t0001g0210 a0001c0001t0001g0249 a0001c0001t0001g0274 others(44): Show |
48 | HG00438.hp1 HG00597.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.71-14300dupG | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952991 | |||||||
chr8:143952994 | C | CG | 82 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(79): Show |
82 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.71-14303_71-14302i others(3): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952994 | |||||||
chr8:143952998 | C | G | 2 | a0004c0178t0003g0138 a0073c0162t0006g0101 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.71-14306G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143952998 | |||||||
chr8:143953042 | A | G | 101 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(98): Show |
101 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.71-14350T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953042 | |||||||
chr8:143953052 | C | A | 1 | a0008c0011t0002g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.71-14360G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953052 | |||||||
chr8:143953248 | C | T | 1 | a0004c0025t0003g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71-14556G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953248 | |||||||
chr8:143953448 | C | CCCG | 28 | a0004c0008t0012g0082 a0004c0178t0003g0138 a0005c0167t0001g0009 others(25): Show |
28 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.71-14759_71-14757d others(5): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953448 | |||||||
chr8:143953448 | C | CCCGCCGC others(5): Show |
3 | a0007c0035t0003g0099 a0011c0156t0003g0105 a0071c0160t0003g0100 |
3 | HG02055.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.71-14768_71-14757d others(14): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953448 | |||||||
chr8:143953477 | T | A | 1 | a0002c0002t0002g0035 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.71-14785A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953477 | |||||||
chr8:143953487 | A | G | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-14795T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953487 | |||||||
chr8:143953704 | G | C | 19 | a0004c0008t0012g0082 a0007c0016t0006g0086 a0007c0016t0006g0087 others(16): Show |
19 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.71-15012C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953704 | |||||||
chr8:143953830 | G | A | 2 | a0002c0002t0002g0032 a0062c0040t0002g0026 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-15138C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953830 | |||||||
chr8:143953835 | G | A | 22 | a0001c0001t0001g0202 a0001c0001t0001g0253 a0001c0013t0001g0001 others(19): Show |
23 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-15143C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953835 | |||||||
chr8:143953899 | G | A | 1 | a0002c0002t0002g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-15207C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953899 | |||||||
chr8:143953921 | G | A | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-15229C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143953921 | |||||||
chr8:143954002 | C | G | 1 | a0001c0104t0001g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.71-15310G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954002 | |||||||
chr8:143954182 | G | C | 3 | a0025c0020t0003g0092 a0025c0020t0003g0093 a0053c0067t0003g0091 |
3 | HG02145.hp1 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.71-15490C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954182 | |||||||
chr8:143954187 | C | A | 1 | a0015c0027t0001g0243 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.71-15495G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954187 | |||||||
chr8:143954330 | C | T | 1 | a0001c0140t0001g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.71-15638G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954330 | |||||||
chr8:143954337 | C | CG | 136 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(133): Show |
136 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.71-15646dupC | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954337 | |||||||
chr8:143954419 | T | C | 137 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(134): Show |
137 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.71-15727A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954419 | |||||||
chr8:143954471 | C | A | 1 | a0077c0142t0001g0266 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.71-15779G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954471 | |||||||
chr8:143954580 | G | A | 1 | a0042c0164t0001g0206 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.71-15888C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954580 | |||||||
chr8:143954606 | A | G | 2 | a0039c0111t0003g0144 a0064c0087t0003g0077 |
2 | HG01346.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.71-15914T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954606 | |||||||
chr8:143954753 | C | G | 19 | a0004c0008t0012g0082 a0007c0016t0006g0086 a0007c0016t0006g0087 others(16): Show |
19 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.71-16061G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954753 | |||||||
chr8:143954769 | C | T | 1 | a0063c0146t0001g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.71-16077G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954769 | |||||||
chr8:143954917 | G | A | 1 | a0001c0128t0001g0234 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.71-16225C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954917 | |||||||
chr8:143954964 | G | C | 22 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(19): Show |
22 | HG01884.hp1 HG02280.hp2 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.71-16272C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143954964 | |||||||
chr8:143955109 | G | A | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-16417C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955109 | |||||||
chr8:143955198 | C | T | 8 | a0002c0005t0002g0041 a0002c0005t0002g0042 a0002c0005t0002g0050 others(5): Show |
8 | HG00597.hp1 HG02056.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-16506G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955198 | |||||||
chr8:143955220 | G | C | 2 | a0002c0002t0002g0032 a0062c0040t0002g0026 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-16528C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955220 | |||||||
chr8:143955248 | AGGTGGAC others(47): Show |
A | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.71-16610_71-16557d others(56): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955248 | |||||||
chr8:143955429 | C | G | 19 | a0004c0008t0012g0082 a0007c0016t0006g0086 a0007c0016t0006g0087 others(16): Show |
19 | HG01175.hp1 HG01192.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.71-16737G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955429 | |||||||
chr8:143955429 | C | T | 1 | a0004c0175t0003g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.71-16737G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955429 | |||||||
chr8:143955594 | G | GT | 8 | a0001c0001t0001g0249 a0001c0006t0001g0235 a0001c0024t0001g0180 others(5): Show |
8 | HG01175.hp1 HG02056.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-16903dupA | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955594 | |||||||
chr8:143955605 | G | T | 1 | a0058c0163t0006g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71-16913C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955605 | |||||||
chr8:143955606 | T | G | 1 | a0058c0163t0006g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71-16914A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955606 | |||||||
chr8:143955609 | TG | T | 11 | a0005c0167t0001g0009 a0007c0035t0003g0099 a0007c0035t0003g0103 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-16918delC | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955609 | |||||||
chr8:143955610 | G | T | 1 | a0058c0163t0006g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71-16918C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955610 | |||||||
chr8:143955944 | C | CT | 14 | a0001c0001t0001g0274 a0001c0132t0001g0215 a0001c0140t0001g0285 others(11): Show |
14 | HG01106.hp1 HG01258.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.71-17253dupA | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955944 | |||||||
chr8:143955944 | CT | C | 105 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(102): Show |
105 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.71-17253delA | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955944 | |||||||
chr8:143955944 | CTT | C | 32 | a0001c0001t0001g0263 a0002c0002t0002g0031 a0002c0002t0002g0035 others(29): Show |
32 | HG01070.hp1 HG01496.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.71-17254_71-17253d others(4): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143955944 | |||||||
chr8:143956076 | C | T | 1 | a0011c0169t0001g0010 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+17327G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143956076 | |||||||
chr8:143956107 | C | T | 1 | a0010c0084t0005g0292 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.70+17296G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143956107 | |||||||
chr8:143956275 | G | A | 13 | a0002c0002t0002g0015 a0002c0002t0002g0108 a0002c0002t0002g0111 others(10): Show |
13 | HG00323.hp1 HG01109.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.70+17128C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143956275 | |||||||
chr8:143956357 | T | C | 31 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(28): Show |
31 | HG01175.hp1 HG01192.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.70+17046A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143956357 | |||||||
chr8:143956404 | C | A | 1 | a0006c0034t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.70+16999G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143956404 | |||||||
chr8:143956612 | G | A | 1 | a0052c0174t0003g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.70+16791C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143956612 | |||||||
chr8:143956732 | TC | T | 63 | a0002c0002t0002g0017 a0002c0002t0002g0020 a0002c0002t0002g0028 others(60): Show |
63 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.70+16670delG | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143956732 | |||||||
chr8:143957074 | C | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+16329G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957074 | |||||||
chr8:143957084 | C | T | 1 | a0001c0072t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.70+16319G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957084 | |||||||
chr8:143957097 | G | A | 134 | a0002c0002t0002g0015 a0002c0002t0002g0017 a0002c0002t0002g0020 others(131): Show |
134 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.70+16306C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957097 | |||||||
chr8:143957135 | C | T | 1 | a0017c0042t0002g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+16268G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957135 | |||||||
chr8:143957254 | C | A | 1 | a0052c0174t0003g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.70+16149G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957254 | |||||||
chr8:143957307 | G | A | 3 | a0004c0178t0003g0138 a0054c0176t0003g0139 a0066c0177t0003g0140 |
3 | HG02258.hp2 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.70+16096C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957307 | |||||||
chr8:143957392 | C | T | 1 | a0005c0003t0004g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.70+16011G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957392 | |||||||
chr8:143957492 | C | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+15911G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957492 | |||||||
chr8:143957630 | T | C | 69 | a0002c0002t0002g0015 a0002c0002t0002g0108 a0002c0002t0002g0111 others(66): Show |
69 | HG00323.hp1 HG01109.hp1 HG01175.hp1 others(66): Show |
intron_variant | MODIFIER | c.70+15773A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957630 | |||||||
chr8:143957759 | C | T | 10 | a0004c0008t0003g0150 a0004c0008t0003g0240 a0004c0008t0003g0255 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.70+15644G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957759 | |||||||
chr8:143957800 | C | T | 66 | a0002c0002t0002g0017 a0002c0002t0002g0020 a0002c0002t0002g0028 others(63): Show |
66 | HG00099.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.70+15603G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957800 | |||||||
chr8:143957897 | C | T | 5 | a0005c0094t0004g0134 a0016c0012t0004g0132 a0016c0012t0004g0133 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+15506G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957897 | |||||||
chr8:143957928 | C | T | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+15475G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957928 | |||||||
chr8:143957944 | A | C | 1 | a0068c0138t0005g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70+15459T>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957944 | |||||||
chr8:143957989 | C | T | 22 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(19): Show |
22 | HG01884.hp1 HG02280.hp2 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.70+15414G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143957989 | |||||||
chr8:143958072 | C | T | 2 | a0001c0024t0001g0180 a0001c0031t0001g0179 |
2 | NA18962.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.70+15331G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958072 | |||||||
chr8:143958134 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0210 a0001c0001t0001g0259 others(140): Show |
145 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.70+15269T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958134 | |||||||
chr8:143958164 | C | CTG | 142 | a0001c0001t0001g0003 a0001c0001t0001g0210 a0001c0001t0001g0259 others(139): Show |
144 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.70+15238_70+15239i others(4): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958164 | |||||||
chr8:143958236 | G | A | 27 | a0004c0008t0012g0082 a0005c0167t0001g0009 a0007c0016t0006g0086 others(24): Show |
27 | HG01175.hp1 HG01192.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.70+15167C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958236 | |||||||
chr8:143958433 | G | A | 12 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(9): Show |
12 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+14970C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958433 | |||||||
chr8:143958463 | C | T | 2 | a0002c0002t0002g0031 a0002c0065t0002g0022 |
2 | HG01074.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.70+14940G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958463 | |||||||
chr8:143958499 | C | G | 1 | a0021c0081t0003g0089 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.70+14904G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958499 | |||||||
chr8:143958575 | C | T | 1 | a0001c0013t0001g0175 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70+14828G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958575 | |||||||
chr8:143958609 | C | A | 2 | a0003c0115t0002g0226 a0006c0150t0002g0231 |
2 | NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.70+14794G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958609 | |||||||
chr8:143958643 | T | TC | 18 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(15): Show |
18 | HG02300.hp1 HG02622.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.70+14759dupG | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958643 | |||||||
chr8:143958812 | C | A | 1 | a0001c0171t0001g0239 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.70+14591G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143958812 | |||||||
chr8:143959395 | G | A | 6 | a0007c0016t0006g0086 a0007c0016t0006g0087 a0007c0016t0006g0295 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+14008C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959395 | |||||||
chr8:143959566 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0063 a0001c0001t0001g0064 others(193): Show |
200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.70+13837C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959566 | |||||||
chr8:143959591 | G | A | 2 | a0001c0133t0001g0170 a0029c0077t0001g0171 |
2 | HG00140.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.70+13812C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959591 | |||||||
chr8:143959608 | C | T | 19 | a0002c0002t0002g0017 a0002c0002t0002g0020 a0002c0002t0002g0028 others(16): Show |
19 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.70+13795G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959608 | |||||||
chr8:143959724 | T | C | 1 | a0087c0125t0001g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.70+13679A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959724 | |||||||
chr8:143959768 | G | A | 4 | a0005c0167t0001g0009 a0010c0022t0005g0011 a0011c0169t0001g0010 others(1): Show |
4 | HG02976.hp2 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+13635C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959768 | |||||||
chr8:143959779 | G | A | 1 | a0084c0102t0002g0149 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.70+13624C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959779 | |||||||
chr8:143959799 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.70+13604T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959799 | |||||||
chr8:143959824 | A | G | 3 | a0001c0028t0001g0267 a0019c0017t0002g0019 a0019c0017t0002g0021 |
3 | HG00741.hp1 HG01070.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.70+13579T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959824 | |||||||
chr8:143959873 | G | A | 1 | a0003c0004t0001g0297 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.70+13530C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143959873 | |||||||
chr8:143960128 | C | T | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+13275G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143960128 | |||||||
chr8:143960310 | A | T | 1 | a0008c0011t0002g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.70+13093T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143960310 | |||||||
chr8:143960331 | A | T | 78 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(75): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.70+13072T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143960331 | |||||||
chr8:143960501 | C | G | 2 | a0009c0007t0005g0076 a0067c0157t0005g0078 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.70+12902G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143960501 | |||||||
chr8:143960684 | G | A | 77 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.70+12719C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143960684 | |||||||
chr8:143960942 | G | A | 1 | a0064c0087t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.70+12461C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143960942 | |||||||
chr8:143960948 | G | A | 1 | a0029c0077t0001g0171 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.70+12455C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143960948 | |||||||
chr8:143961042 | A | G | 5 | a0001c0001t0001g0174 a0001c0001t0001g0227 a0001c0001t0001g0283 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+12361T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143961042 | |||||||
chr8:143961174 | A | G | 113 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(110): Show |
113 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.70+12229T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143961174 | |||||||
chr8:143961230 | C | CT | 79 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(76): Show |
79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.70+12172dupA | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143961230 | |||||||
chr8:143961251 | A | G | 19 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(16): Show |
19 | HG01884.hp1 HG02300.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.70+12152T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143961251 | |||||||
chr8:143961311 | C | T | 2 | a0001c0133t0001g0170 a0029c0077t0001g0171 |
2 | HG00140.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.70+12092G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143961311 | |||||||
chr8:143961315 | T | G | 16 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.70+12088A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143961315 | |||||||
chr8:143961840 | A | G | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+11563T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143961840 | |||||||
chr8:143962304 | G | A | 1 | a0030c0129t0001g0233 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.70+11099C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962304 | |||||||
chr8:143962309 | C | CGGCT | 5 | a0005c0094t0004g0134 a0016c0012t0004g0132 a0016c0012t0004g0133 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+11090_70+11093d others(6): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962309 | |||||||
chr8:143962425 | C | T | 1 | a0030c0129t0001g0233 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.70+10978G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962425 | |||||||
chr8:143962447 | T | C | 97 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(94): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.70+10956A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962447 | |||||||
chr8:143962504 | C | T | 1 | a0077c0142t0001g0266 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.70+10899G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962504 | |||||||
chr8:143962623 | G | A | 1 | a0070c0093t0004g0129 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.70+10780C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962623 | |||||||
chr8:143962746 | T | C | 1 | a0010c0022t0005g0294 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70+10657A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962746 | |||||||
chr8:143962842 | A | G | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.70+10561T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962842 | |||||||
chr8:143962844 | G | A | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.70+10559C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962844 | |||||||
chr8:143962845 | A | G | 1 | a0055c0068t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.70+10558T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143962845 | |||||||
chr8:143963022 | C | T | 3 | a0001c0032t0001g0066 a0002c0002t0002g0067 a0002c0037t0002g0065 |
3 | HG00408.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.70+10381G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143963022 | |||||||
chr8:143963405 | T | A | 78 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(75): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.70+9998A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143963405 | |||||||
chr8:143963809 | A | AT | 64 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0247 others(61): Show |
64 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.70+9593dupA | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143963809 | |||||||
chr8:143963809 | A | ATT | 35 | a0002c0002t0002g0017 a0002c0002t0002g0020 a0002c0002t0002g0028 others(32): Show |
35 | HG00099.hp2 HG01070.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.70+9592_70+9593dup others(2): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143963809 | |||||||
chr8:143963809 | AT | A | 13 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0069t0001g0228 others(10): Show |
13 | HG01069.hp1 HG01975.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.70+9593delA | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143963809 | |||||||
chr8:143964056 | A | G | 1 | a0001c0118t0001g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.70+9347T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143964056 | |||||||
chr8:143964444 | C | G | 2 | a0001c0001t0001g0164 a0001c0106t0001g0244 |
2 | HG00423.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.70+8959G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143964444 | |||||||
chr8:143964533 | C | T | 2 | a0015c0027t0001g0243 a0015c0107t0001g0157 |
2 | HG02080.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.70+8870G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143964533 | |||||||
chr8:143964649 | C | T | 1 | a0039c0111t0003g0144 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.70+8754G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143964649 | |||||||
chr8:143964700 | T | C | 1 | a0023c0135t0001g0232 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.70+8703A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143964700 | |||||||
chr8:143964794 | C | G | 2 | a0009c0007t0005g0076 a0067c0157t0005g0078 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.70+8609G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143964794 | |||||||
chr8:143964997 | A | AC | 23 | a0001c0032t0001g0162 a0001c0131t0002g0163 a0001c0149t0001g0242 others(20): Show |
23 | HG00639.hp2 HG01109.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+8405dupG | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143964997 | |||||||
chr8:143965013 | T | A | 1 | a0001c0001t0001g0259 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.70+8390A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965013 | |||||||
chr8:143965232 | T | C | 77 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.70+8171A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965232 | |||||||
chr8:143965287 | G | A | 1 | a0006c0034t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.70+8116C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965287 | |||||||
chr8:143965334 | G | A | 1 | a0030c0129t0001g0233 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.70+8069C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965334 | |||||||
chr8:143965399 | C | T | 1 | a0001c0009t0001g0296 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70+8004G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965399 | |||||||
chr8:143965427 | T | TCCACCTG others(18): Show |
115 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(112): Show |
115 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.70+7975_70+7976ins others(25): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965427 | |||||||
chr8:143965695 | G | T | 19 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(16): Show |
19 | HG01884.hp1 HG02300.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.70+7708C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965695 | |||||||
chr8:143965810 | C | T | 1 | a0005c0095t0004g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70+7593G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965810 | |||||||
chr8:143965841 | A | T | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+7562T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965841 | |||||||
chr8:143965940 | T | C | 77 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.70+7463A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143965940 | |||||||
chr8:143966054 | C | T | 1 | a0036c0057t0002g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70+7349G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966054 | |||||||
chr8:143966162 | A | G | 1 | a0064c0087t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.70+7241T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966162 | |||||||
chr8:143966188 | T | C | 20 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(17): Show |
20 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.70+7215A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966188 | |||||||
chr8:143966399 | C | G | 78 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(75): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.70+7004G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966399 | |||||||
chr8:143966428 | A | G | 1 | a0002c0058t0002g0023 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.70+6975T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966428 | |||||||
chr8:143966622 | C | CCTGCCAC others(74): Show |
1 | a0065c0070t0003g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.70+6780_70+6781ins others(81): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966622 | |||||||
chr8:143966639 | C | T | 4 | a0010c0022t0005g0294 a0010c0083t0005g0293 a0010c0084t0005g0292 others(1): Show |
4 | HG01175.hp1 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+6764G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966639 | |||||||
chr8:143966687 | C | T | 1 | a0064c0087t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.70+6716G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966687 | |||||||
chr8:143966688 | G | T | 71 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(68): Show |
71 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.70+6715C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966688 | |||||||
chr8:143966798 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.70+6605A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966798 | |||||||
chr8:143966858 | A | G | 1 | a0012c0015t0001g0160 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.70+6545T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966858 | |||||||
chr8:143966936 | A | T | 1 | a0034c0101t0002g0159 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.70+6467T>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966936 | |||||||
chr8:143966984 | A | G | 12 | a0002c0002t0002g0015 a0002c0002t0002g0108 a0002c0002t0002g0111 others(9): Show |
12 | HG00323.hp1 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+6419T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143966984 | |||||||
chr8:143967102 | G | A | 8 | a0001c0006t0001g0145 a0001c0006t0001g0235 a0001c0006t0001g0237 others(5): Show |
8 | HG01123.hp2 HG01358.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+6301C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967102 | |||||||
chr8:143967165 | T | C | 134 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0241 others(131): Show |
134 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.70+6238A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967165 | |||||||
chr8:143967224 | A | G | 1 | a0064c0087t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.70+6179T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967224 | |||||||
chr8:143967280 | T | G | 1 | a0002c0053t0002g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70+6123A>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967280 | |||||||
chr8:143967352 | G | GACTCCAT others(2320): Show |
1 | a0001c0001t0001g0283 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.70+6050_70+6051ins others(2327): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967352 | |||||||
chr8:143967362 | C | CA | 34 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(31): Show |
35 | HG00597.hp2 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.70+6040dupT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967362 | |||||||
chr8:143967362 | CA | C | 36 | a0001c0001t0001g0063 a0001c0001t0001g0272 a0001c0112t0001g0273 others(33): Show |
36 | HG00741.hp2 HG01175.hp2 HG01516.hp2 others(33): Show |
intron_variant | MODIFIER | c.70+6040delT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967362 | |||||||
chr8:143967362 | CAA | C | 62 | a0001c0032t0001g0066 a0002c0002t0002g0017 a0002c0002t0002g0020 others(59): Show |
62 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.70+6039_70+6040del others(2): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967362 | |||||||
chr8:143967362 | CAAAAAAA others(2): Show |
C | 16 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.70+6032_70+6040del others(9): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967362 | |||||||
chr8:143967386 | A | G | 1 | a0009c0007t0005g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.70+6017T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967386 | |||||||
chr8:143967532 | T | A | 1 | a0001c0009t0001g0296 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70+5871A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967532 | |||||||
chr8:143967636 | A | G | 14 | a0004c0008t0012g0082 a0007c0016t0006g0086 a0007c0016t0006g0087 others(11): Show |
14 | HG01192.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.70+5767T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967636 | |||||||
chr8:143967775 | T | C | 5 | a0001c0140t0001g0285 a0001c0141t0001g0262 a0006c0034t0001g0282 others(2): Show |
5 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+5628A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967775 | |||||||
chr8:143967833 | A | G | 3 | a0002c0002t0002g0031 a0002c0053t0002g0068 a0002c0065t0002g0022 |
3 | HG01074.hp2 HG01517.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.70+5570T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143967833 | |||||||
chr8:143968137 | C | CA | 20 | a0001c0001t0001g0263 a0005c0003t0004g0014 a0005c0003t0004g0122 others(17): Show |
20 | HG00597.hp2 HG01884.hp1 HG02300.hp1 others(17): Show |
intron_variant | MODIFIER | c.70+5265dupT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968137 | |||||||
chr8:143968168 | T | C | 12 | a0002c0002t0002g0015 a0002c0002t0002g0108 a0002c0002t0002g0111 others(9): Show |
12 | HG00323.hp1 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+5235A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968168 | |||||||
chr8:143968306 | C | T | 3 | a0020c0026t0002g0155 a0020c0026t0002g0156 a0078c0100t0002g0154 |
3 | HG01070.hp2 HG01071.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.70+5097G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968306 | |||||||
chr8:143968501 | G | A | 3 | a0001c0032t0001g0066 a0002c0002t0002g0067 a0002c0037t0002g0065 |
3 | HG00408.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.70+4902C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968501 | |||||||
chr8:143968529 | C | CA | 7 | a0001c0028t0001g0267 a0001c0136t0001g0268 a0003c0004t0001g0297 others(4): Show |
7 | HG00639.hp2 HG01256.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+4873dupT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968529 | |||||||
chr8:143968529 | C | CAAAAAAA others(1): Show |
15 | a0002c0002t0002g0028 a0002c0002t0002g0137 a0002c0047t0002g0018 others(12): Show |
15 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+4866_70+4873dup others(8): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968529 | |||||||
chr8:143968529 | C | CAAAAAAA others(2): Show |
85 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(82): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.70+4865_70+4873dup others(9): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968529 | |||||||
chr8:143968529 | C | CAAAAAAA others(3): Show |
11 | a0002c0002t0002g0070 a0002c0002t0002g0071 a0002c0005t0002g0069 others(8): Show |
11 | HG01192.hp1 HG02145.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+4864_70+4873dup others(10): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968529 | |||||||
chr8:143968529 | C | CAAAAAAA others(4): Show |
1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+4863_70+4873dup others(11): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968529 | |||||||
chr8:143968529 | CA | C | 14 | a0001c0001t0001g0272 a0002c0002t0002g0015 a0002c0002t0002g0108 others(11): Show |
14 | HG00323.hp1 HG01109.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.70+4873delT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968529 | |||||||
chr8:143968530 | A | AAAAAAAA others(3): Show |
1 | a0065c0070t0003g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.70+4872_70+4873ins others(10): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968530 | |||||||
chr8:143968636 | T | C | 12 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+4767A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968636 | |||||||
chr8:143968923 | C | T | 13 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.70+4480G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143968923 | |||||||
chr8:143969164 | C | T | 1 | a0088c0099t0004g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.70+4239G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969164 | |||||||
chr8:143969199 | C | T | 1 | a0002c0047t0002g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.70+4204G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969199 | |||||||
chr8:143969276 | T | C | 1 | a0038c0144t0001g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.70+4127A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969276 | |||||||
chr8:143969307 | C | T | 1 | a0001c0118t0001g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.70+4096G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969307 | |||||||
chr8:143969312 | C | G | 1 | a0003c0113t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70+4091G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969312 | |||||||
chr8:143969374 | C | A | 1 | a0072c0158t0004g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70+4029G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969374 | |||||||
chr8:143969375 | A | G | 114 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0272 others(111): Show |
114 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.70+4028T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969375 | |||||||
chr8:143969405 | C | T | 3 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 |
3 | HG02280.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.70+3998G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969405 | |||||||
chr8:143969479 | C | G | 6 | a0005c0167t0001g0009 a0010c0022t0005g0011 a0011c0169t0001g0010 others(3): Show |
6 | HG02922.hp2 HG02976.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.70+3924G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969479 | |||||||
chr8:143969519 | G | A | 1 | a0063c0146t0001g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.70+3884C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969519 | |||||||
chr8:143969713 | G | A | 5 | a0005c0094t0004g0134 a0016c0012t0004g0132 a0016c0012t0004g0133 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+3690C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969713 | |||||||
chr8:143969819 | C | T | 3 | a0025c0020t0003g0092 a0025c0020t0003g0093 a0053c0067t0003g0091 |
3 | HG02145.hp1 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.70+3584G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969819 | |||||||
chr8:143969903 | G | A | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+3500C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969903 | |||||||
chr8:143969916 | G | C | 2 | a0001c0001t0001g0272 a0001c0112t0001g0273 |
2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.70+3487C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969916 | |||||||
chr8:143969936 | C | T | 119 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(116): Show |
119 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.70+3467G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143969936 | |||||||
chr8:143970155 | G | C | 1 | a0014c0064t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.70+3248C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970155 | |||||||
chr8:143970298 | C | CA | 8 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0006t0001g0277 others(5): Show |
8 | HG01934.hp2 HG01993.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.70+3104dupT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970298 | |||||||
chr8:143970298 | CA | C | 16 | a0001c0001t0010g0148 a0002c0002t0002g0017 a0003c0113t0001g0147 others(13): Show |
16 | HG01081.hp1 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.70+3104delT | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970298 | |||||||
chr8:143970298 | CAA | C | 11 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(8): Show |
11 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+3103_70+3104del others(2): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970298 | |||||||
chr8:143970324 | G | A | 1 | a0060c0159t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+3079C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970324 | |||||||
chr8:143970376 | G | A | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+3027C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970376 | |||||||
chr8:143970581 | A | G | 131 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(128): Show |
131 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.70+2822T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970581 | |||||||
chr8:143970613 | G | A | 1 | a0003c0148t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.70+2790C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970613 | |||||||
chr8:143970808 | C | A | 2 | a0089c0155t0001g0281 a0091c0154t0001g0280 |
2 | NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.70+2595G>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970808 | |||||||
chr8:143970847 | C | T | 1 | a0080c0147t0001g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.70+2556G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143970847 | |||||||
chr8:143971068 | G | A | 2 | a0006c0034t0001g0282 a0014c0062t0001g0106 |
2 | HG03195.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.70+2335C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971068 | |||||||
chr8:143971089 | C | T | 15 | a0004c0008t0012g0082 a0007c0016t0006g0086 a0007c0016t0006g0087 others(12): Show |
15 | HG01192.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.70+2314G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971089 | |||||||
chr8:143971098 | C | T | 1 | a0001c0006t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70+2305G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971098 | |||||||
chr8:143971356 | G | T | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+2047C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971356 | |||||||
chr8:143971357 | C | T | 1 | a0014c0062t0001g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+2046G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971357 | |||||||
chr8:143971412 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.70+1991C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971412 | |||||||
chr8:143971628 | C | T | 15 | a0004c0025t0003g0094 a0004c0025t0003g0095 a0004c0096t0003g0096 others(12): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.70+1775G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971628 | |||||||
chr8:143971629 | G | A | 1 | a0048c0092t0001g0284 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.70+1774C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971629 | |||||||
chr8:143971855 | G | C | 1 | a0013c0010t0002g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.70+1548C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971855 | |||||||
chr8:143971991 | G | A | 1 | a0068c0138t0005g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70+1412C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143971991 | |||||||
chr8:143972104 | C | T | 1 | a0039c0111t0003g0144 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.70+1299G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972104 | |||||||
chr8:143972200 | C | T | 1 | a0001c0104t0001g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.70+1203G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972200 | |||||||
chr8:143972227 | C | G | 2 | a0004c0073t0008g0141 a0004c0074t0008g0142 |
2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.70+1176G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972227 | |||||||
chr8:143972232 | C | T | 3 | a0025c0020t0003g0092 a0025c0020t0003g0093 a0053c0067t0003g0091 |
3 | HG02145.hp1 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.70+1171G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972232 | |||||||
chr8:143972325 | T | C | 1 | a0001c0140t0001g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.70+1078A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972325 | |||||||
chr8:143972360 | T | TGGGCACA others(14): Show |
1 | a0068c0138t0005g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70+1022_70+1042dup others(21): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972360 | |||||||
chr8:143972419 | G | A | 15 | a0004c0008t0012g0082 a0007c0016t0006g0086 a0007c0016t0006g0087 others(12): Show |
15 | HG01192.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.70+984C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972419 | |||||||
chr8:143972494 | C | T | 77 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(74): Show |
77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.70+909G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972494 | |||||||
chr8:143972541 | G | T | 1 | a0002c0002t0002g0015 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.70+862C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972541 | |||||||
chr8:143972567 | G | A | 1 | a0004c0175t0003g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.70+836C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972567 | |||||||
chr8:143972600 | T | C | 3 | a0004c0008t0003g0289 a0011c0088t0003g0290 a0011c0089t0003g0288 |
3 | HG02257.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.70+803A>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972600 | |||||||
chr8:143972663 | G | C | 5 | a0007c0016t0006g0295 a0010c0022t0005g0294 a0010c0083t0005g0293 others(2): Show |
5 | HG01175.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+740C>G | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972663 | |||||||
chr8:143972679 | T | A | 19 | a0005c0003t0004g0014 a0005c0003t0004g0122 a0005c0003t0004g0123 others(16): Show |
19 | HG01884.hp1 HG02300.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.70+724A>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972679 | |||||||
chr8:143972697 | C | T | 3 | a0004c0178t0003g0138 a0054c0176t0003g0139 a0066c0177t0003g0140 |
3 | HG02258.hp2 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.70+706G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972697 | |||||||
chr8:143972698 | G | A | 2 | a0002c0002t0002g0136 a0002c0002t0002g0137 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.70+705C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972698 | |||||||
chr8:143972904 | A | ACAGAGAA others(76): Show |
1 | a0005c0003t0004g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.70+416_70+498dupGC others(81): Show |
PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143972904 | |||||||
chr8:143973019 | A | G | 131 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0032t0001g0066 others(128): Show |
131 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.70+384T>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143973019 | |||||||
chr8:143973125 | C | T | 5 | a0005c0167t0001g0009 a0010c0022t0005g0011 a0011c0169t0001g0010 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+278G>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143973125 | |||||||
chr8:143973132 | C | G | 1 | a0006c0014t0001g0008 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.70+271G>C | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143973132 | |||||||
chr8:143973219 | G | T | 2 | a0043c0091t0003g0006 a0072c0158t0004g0007 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.70+184C>A | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143973219 | |||||||
chr8:143973278 | G | A | 1 | a0001c0009t0001g0296 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70+125C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143973278 | |||||||
chr8:143973313 | G | A | 1 | a0003c0004t0001g0297 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.70+90C>T | PLEC | ENSG00000178209.17 | transcript | ENST00000356346.7 | protein_coding | 1/31 | chr8 | 143973313 |