geneid | 5495 |
---|---|
ensemblid | ENSG00000138032.21 |
hgncid | 9276 |
symbol | PPM1B |
name | protein phosphatase, Mg2+/Mn2+ dependent 1B |
refseq_nuc | NM_002706.6 |
refseq_prot | NP_002697.1 |
ensembl_nuc | ENST00000282412.9 |
ensembl_prot | ENSP00000282412.4 |
mane_status | MANE Select |
chr | chr2 |
start | 44168875 |
end | 44231472 |
strand | + |
ver | v1.2 |
region | chr2:44168875-44231472 |
region5000 | chr2:44163875-44236472 |
regionname0 | PPM1B_chr2_44168875_44231472 |
regionname5000 | PPM1B_chr2_44163875_44236472 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 479 | 352 | 89 | 64 | 154 | 12 | 31 | 120 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0002 | 0/0 | 479 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0003 | 0/0 | 479 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0004 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1440 | 352 | 89 | 64 | 154 | 12 | 31 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
c0002 | 0/0 | 1440 | 4 | 4 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
c0003 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
c0004 | 0/0 | 1440 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1178 | 263 | 73 | 43 | 107 | 11 | 28 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0002 | 1/0 | 1169 | 75 | 13 | 15 | 43 | 1 | 2 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0003 | 0/0 | 1187 | 5 | 5 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0004 | 0/0 | 1178 | 4 | 0 | 4 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0005 | 0/0 | 1178 | 4 | 0 | 0 | 4 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0006 | 0/0 | 1178 | 2 | 2 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0007 | 0/0 | 1178 | 2 | 0 | 2 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0008 | 0/0 | 1187 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0009 | 0/0 | 1178 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
t0010 | 0/0 | 1169 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1440 | 352 | 89 | 64 | 154 | 12 | 31 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0002c0002 | 0/0 | 1440 | 4 | 4 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0003c0004 | 0/0 | 1440 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0004c0003 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2617 | 257 | 68 | 43 | 107 | 11 | 27 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0002 | 1/0 | 2608 | 75 | 13 | 15 | 43 | 1 | 2 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0003 | 0/0 | 2626 | 5 | 5 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0004 | 0/0 | 2617 | 4 | 0 | 4 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0005 | 0/0 | 2617 | 4 | 0 | 0 | 4 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0006 | 0/0 | 2617 | 2 | 2 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0007 | 0/0 | 2617 | 2 | 0 | 2 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0008 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0009 | 0/0 | 2617 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0001c0001t0010 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0002c0002t0001 | 0/0 | 2617 | 4 | 4 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0003c0004t0001 | 0/0 | 2617 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
a0004c0003t0001 | 0/0 | 2617 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | copy fasta | chr2 | 44163875 | 44236472 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0003c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
a0004c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0084 | EUR | FIN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01069 | hp2 | a0001 | c0001 | t0007 | g0218 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0219 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0300 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0297 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02155 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02683 | hp1 | a0001 | c0001 | t0010 | g0049 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0348 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0346 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0347 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03704 | hp1 | a0003 | c0004 | t0001 | g0296 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG04228 | hp1 | a0001 | c0001 | t0009 | g0065 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0266 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0339 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | GIH | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG02559 | hp2 | a0004 | c0003 | t0001 | g0013 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0335 | REF | REF | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0086 | REF | REF | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44201251
|
G | A | 1 | a0002 | 4 | HG02622.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.52G>A | p.Ala18Thr | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | 466/2608 | 52/1440 | 18/479 | chr2 | 44201251 | ||
chr2:44201266
|
C | T | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.67C>T | p.Arg23Cys | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | 481/2608 | 67/1440 | 23/479 | chr2 | 44201266 | ||
chr2:44218530
|
G | A | 1 | a0004 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1127G>A | p.Ser376Asn | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/6 | 1541/2608 | 1127/1440 | 376/479 | chr2 | 44218530 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44168923
|
G | T | 1 | a0001c0001t0007 | 2 | HG01069.hp2 HG01071.hp2 |
5_prime_UTR_variant | MODIFIER | c.-366G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32277 | chr2 | 44168923 | |||||
chr2:44169029
|
G | A | 1 | a0001c0001t0008 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-260G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32171 | chr2 | 44169029 | |||||
chr2:44169088
|
A | AGGCGGCA others(2): Show |
2 | a0001c0001t0003a0001c0001t0008 | 6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-194_-193insGCGGCG others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32104 | INFO_REALIGN_3_PRIME | chr2 | 44169088 | ||||
chr2:44169096
|
T | G | 10 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | 281 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(278): Show |
5_prime_UTR_variant | MODIFIER | c.-193T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32104 | chr2 | 44169096 | |||||
chr2:44169140
|
C | CCGGAGGC others(2): Show |
11 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(8): Show | 282 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(279): Show |
5_prime_UTR_variant | MODIFIER | c.-145_-137dupAGGCGG others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32047 | INFO_REALIGN_3_PRIME | chr2 | 44169140 | ||||
chr2:44169269
|
C | T | 1 | a0001c0001t0006 | 2 | HG02647.hp2 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-20C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 31931 | chr2 | 44169269 | |||||
chr2:44201196
|
A | G | 1 | a0001c0001t0008 | 1 | NA20300.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-4A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | chr2 | 44201196 | ||||||
chr2:44201199
|
C | T | 1 | a0001c0001t0010 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | 1 | chr2 | 44201199 | |||||
chr2:44230781
|
T | C | 1 | a0001c0001t0004 | 4 | HG01081.hp1 HG01106.hp2 HG01952.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*63T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 6/6 | 63 | chr2 | 44230781 | |||||
chr2:44230999
|
A | G | 1 | a0001c0001t0005 | 4 | HG00544.hp1 HG02155.hp1 NA18943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*281A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 6/6 | 281 | chr2 | 44230999 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44169316
|
C | T | 1 | a0001c0001t0001g0349 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-15+42C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169316 | ||||||
chr2:44169337
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15+63G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169337 | ||||||
chr2:44169363
|
T | G | 1 | a0001c0001t0001g0010 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-15+89T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169363 | ||||||
chr2:44169385
|
C | G | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+111C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169385 | ||||||
chr2:44169480
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+206C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169480 | ||||||
chr2:44169628
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15+354C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169628 | ||||||
chr2:44169646
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+372G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169646 | ||||||
chr2:44169674
|
T | A | 1 | a0001c0001t0002g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-15+400T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169674 | ||||||
chr2:44169716
|
C | G | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG00621.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-15+442C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169716 | ||||||
chr2:44169770
|
C | G | 1 | a0001c0001t0001g0340 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15+496C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169770 | ||||||
chr2:44169905
|
A | G | 170 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 173 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-15+631A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169905 | ||||||
chr2:44169941
|
TTAAGAG | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+670_-15+675del others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44169941 | |||||
chr2:44170108
|
T | A | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+834T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170108 | ||||||
chr2:44170166
|
T | A | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-15+892T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170166 | ||||||
chr2:44170220
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-15+946A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170220 | ||||||
chr2:44170423
|
A | G | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1149A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170423 | ||||||
chr2:44170433
|
T | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00438.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-15+1159T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170433 | ||||||
chr2:44170476
|
A | G | 5 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(2): Show | 5 | HG03017.hp1 HG03239.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+1202A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170476 | ||||||
chr2:44170486
|
A | C | 1 | a0001c0001t0001g0335 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-15+1212A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170486 | ||||||
chr2:44170672
|
ATTG | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0027a0002c0002t0001g0024others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1402_-15+1404d others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44170672 | |||||
chr2:44170731
|
A | C | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+1457A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170731 | ||||||
chr2:44170768
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0178a0001c0001t0001g0179others(3): Show | 7 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+1494T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170768 | ||||||
chr2:44170871
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15+1597T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170871 | ||||||
chr2:44170887
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 83 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.-15+1613A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170887 | ||||||
chr2:44170938
|
C | G | 1 | a0001c0001t0001g0331 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+1664C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170938 | ||||||
chr2:44170973
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+1699G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170973 | ||||||
chr2:44170983
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15+1709C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170983 | ||||||
chr2:44170988
|
CATTT | C | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1715_-15+1718d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170988 | ||||||
chr2:44171018
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-15+1744A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171018 | ||||||
chr2:44171116
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+1842T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171116 | ||||||
chr2:44171238
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-15+1964A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171238 | ||||||
chr2:44171250
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+1976C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171250 | ||||||
chr2:44171292
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15+2018A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171292 | ||||||
chr2:44171310
|
A | G | 1 | a0001c0001t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+2036A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171310 | ||||||
chr2:44171347
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+2073T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171347 | ||||||
chr2:44171502
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+2228G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171502 | ||||||
chr2:44171528
|
C | G | 1 | a0001c0001t0001g0340 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15+2254C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171528 | ||||||
chr2:44171585
|
T | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0104others(53): Show | 58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15+2311T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171585 | ||||||
chr2:44171777
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+2503C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171777 | ||||||
chr2:44171829
|
C | CA | 23 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0027others(20): Show | 23 | HG00741.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15+2578dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44171829 | |||||
chr2:44171829
|
CA | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 74 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-15+2578delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44171829 | |||||
chr2:44171829
|
CAAAAAAA others(1): Show |
C | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 167 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.-15+2571_-15+2578d others(10): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44171829 | |||||
chr2:44171852
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+2578A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171852 | ||||||
chr2:44171954
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+2680T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171954 | ||||||
chr2:44171996
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 7 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+2722T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171996 | ||||||
chr2:44171997
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+2723G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171997 | ||||||
chr2:44172082
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+2808A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172082 | ||||||
chr2:44172196
|
C | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-15+2922C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172196 | ||||||
chr2:44172199
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-15+2925G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172199 | ||||||
chr2:44172242
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+2968G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172242 | ||||||
chr2:44172336
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-15+3062C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172336 | ||||||
chr2:44172359
|
C | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+3085C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172359 | ||||||
chr2:44172361
|
T | A | 1 | a0001c0001t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-15+3087T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172361 | ||||||
chr2:44172497
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-15+3223C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172497 | ||||||
chr2:44172551
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+3277C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172551 | ||||||
chr2:44172762
|
C | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+3488C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172762 | ||||||
chr2:44172783
|
C | T | 1 | a0001c0001t0001g0329 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-15+3509C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172783 | ||||||
chr2:44172980
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+3706C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172980 | ||||||
chr2:44173031
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-15+3757G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173031 | ||||||
chr2:44173041
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-15+3767G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173041 | ||||||
chr2:44173074
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+3800G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173074 | ||||||
chr2:44173220
|
G | T | 15 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+3946G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173220 | ||||||
chr2:44173384
|
CT | C | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+4117delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44173384 | |||||
chr2:44173430
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+4156G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173430 | ||||||
chr2:44173508
|
C | G | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15+4234C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173508 | ||||||
chr2:44173534
|
G | C | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+4260G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173534 | ||||||
chr2:44173610
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+4336A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173610 | ||||||
chr2:44173634
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+4360T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173634 | ||||||
chr2:44173659
|
A | C | 187 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 190 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-15+4385A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173659 | ||||||
chr2:44173791
|
A | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+4517A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173791 | ||||||
chr2:44173916
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 280 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.-15+4642T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173916 | ||||||
chr2:44173943
|
G | A | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG03654.hp2 NA18964.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+4669G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173943 | ||||||
chr2:44174213
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-15+4939C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174213 | ||||||
chr2:44174213
|
C | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-15+4939C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174213 | ||||||
chr2:44174289
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+5015A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174289 | ||||||
chr2:44174423
|
T | C | 339 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(336): Show | 348 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.-15+5149T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174423 | ||||||
chr2:44174456
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-15+5182T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174456 | ||||||
chr2:44174642
|
T | G | 1 | a0001c0001t0002g0042 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-15+5368T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174642 | ||||||
chr2:44174704
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 276 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.-15+5430C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174704 | ||||||
chr2:44174963
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-15+5689A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174963 | ||||||
chr2:44174975
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+5701C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174975 | ||||||
chr2:44175119
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0027a0002c0002t0001g0024others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5845C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175119 | ||||||
chr2:44175322
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-15+6048A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175322 | ||||||
chr2:44175328
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 277 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.-15+6054T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175328 | ||||||
chr2:44175591
|
T | A | 7 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG00597.hp1 HG02165.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+6317T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175591 | ||||||
chr2:44175625
|
G | C | 1 | a0001c0001t0002g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-15+6351G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175625 | ||||||
chr2:44175643
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+6369C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175643 | ||||||
chr2:44175785
|
A | AT | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 146 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-15+6529dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44175785 | |||||
chr2:44175785
|
A | ATT | 26 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0139others(23): Show | 26 | HG00621.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+6528_-15+6529d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44175785 | |||||
chr2:44175846
|
T | C | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+6572T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175846 | ||||||
chr2:44175986
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-15+6712A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175986 | ||||||
chr2:44176072
|
C | G | 162 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 165 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.-15+6798C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176072 | ||||||
chr2:44176175
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+6901A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176175 | ||||||
chr2:44176220
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15+6946G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176220 | ||||||
chr2:44176269
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-15+6995C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176269 | ||||||
chr2:44176344
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-15+7070G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176344 | ||||||
chr2:44176504
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+7230G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176504 | ||||||
chr2:44176550
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+7276G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176550 | ||||||
chr2:44176665
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-15+7391A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176665 | ||||||
chr2:44176737
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+7463G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176737 | ||||||
chr2:44176786
|
C | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0027a0002c0002t0001g0024others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+7512C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176786 | ||||||
chr2:44176929
|
C | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(56): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+7655C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176929 | ||||||
chr2:44176937
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+7663C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176937 | ||||||
chr2:44176991
|
G | C | 1 | a0001c0001t0002g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-15+7717G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176991 | ||||||
chr2:44177026
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-15+7752C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177026 | ||||||
chr2:44177075
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+7801C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177075 | ||||||
chr2:44177134
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+7860A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177134 | ||||||
chr2:44177142
|
G | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+7868G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177142 | ||||||
chr2:44177148
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+7874G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177148 | ||||||
chr2:44177151
|
A | T | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(181): Show | 187 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-15+7877A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177151 | ||||||
chr2:44177226
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+7952T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177226 | ||||||
chr2:44177418
|
C | CT | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(18): Show | 21 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+8161dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | |||||
chr2:44177418
|
C | CTT | 161 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 164 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-15+8160_-15+8161d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | |||||
chr2:44177418
|
C | CTTT | 12 | a0001c0001t0001g0004a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 13 | HG00642.hp2 HG01070.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+8159_-15+8161d others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | |||||
chr2:44177418
|
C | CTTTT | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(66): Show | 72 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-15+8158_-15+8161d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | |||||
chr2:44177452
|
CTT | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+8179_-15+8180d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177452 | ||||||
chr2:44177470
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-15+8196G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177470 | ||||||
chr2:44177471
|
T | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-15+8197T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177471 | ||||||
chr2:44177542
|
G | C | 3 | a0001c0001t0001g0152a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+8268G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177542 | ||||||
chr2:44177544
|
G | C | 3 | a0001c0001t0001g0152a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+8270G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177544 | ||||||
chr2:44177700
|
G | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+8426G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177700 | ||||||
chr2:44177763
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 273 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.-15+8489T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177763 | ||||||
chr2:44177915
|
C | CT | 23 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0150others(20): Show | 25 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+8660dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177915 | |||||
chr2:44177915
|
CT | C | 11 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 11 | HG00323.hp1 HG00609.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+8660delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177915 | |||||
chr2:44177926
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+8652T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177926 | ||||||
chr2:44177934
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+8660T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177934 | ||||||
chr2:44177963
|
G | T | 9 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(6): Show | 9 | HG00408.hp2 NA18980.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+8689G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177963 | ||||||
chr2:44178024
|
C | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG00609.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-15+8750C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178024 | ||||||
chr2:44178093
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-15+8819T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178093 | ||||||
chr2:44178199
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-15+8925C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178199 | ||||||
chr2:44178399
|
C | T | 1 | a0001c0001t0003g0347 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-15+9125C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178399 | ||||||
chr2:44178452
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-15+9178G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178452 | ||||||
chr2:44178452
|
G | GTA | 7 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0329others(4): Show | 7 | HG00323.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+9200_-15+9201d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178452 | |||||
chr2:44178452
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+9179_-15+9180i others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178452 | |||||
chr2:44178452
|
GTA | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0170others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+9200_-15+9201d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178452 | |||||
chr2:44178454
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0002g0043 | 2 | HG03195.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-15+9180A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178454 | ||||||
chr2:44178472
|
A | T | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+9198A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178472 | ||||||
chr2:44178474
|
A | ATATT | 26 | a0001c0001t0001g0004a0001c0001t0001g0102a0001c0001t0001g0104others(23): Show | 27 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15+9201_-15+9202i others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | |||||
chr2:44178474
|
A | ATT | 6 | a0001c0001t0001g0023a0001c0001t0001g0314a0002c0002t0001g0024others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+9210_-15+9211d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | |||||
chr2:44178474
|
A | ATTT | 9 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 11 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+9209_-15+9211d others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | |||||
chr2:44178474
|
A | ATTTT | 29 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(26): Show | 30 | HG00621.hp1 HG01070.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+9208_-15+9211d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | |||||
chr2:44178474
|
A | T | 6 | a0001c0001t0001g0115a0001c0001t0002g0090a0001c0001t0003g0345others(3): Show | 6 | HG00609.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+9200A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178474 | ||||||
chr2:44178474
|
AT | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(151): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-15+9211delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | |||||
chr2:44178474
|
ATT | A | 8 | a0001c0001t0001g0096a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01074.hp2 HG01099.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+9210_-15+9211d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | |||||
chr2:44178475
|
T | TA | 4 | a0001c0001t0001g0007a0001c0001t0001g0195a0001c0001t0001g0215others(1): Show | 5 | HG01175.hp1 HG01433.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+9201_-15+9202i others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178475 | ||||||
chr2:44178476
|
T | A | 15 | a0001c0001t0001g0031a0001c0001t0001g0168a0001c0001t0001g0169others(12): Show | 15 | HG02074.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+9202T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178476 | ||||||
chr2:44178477
|
T | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0336 | 2 | HG03017.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-15+9203T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178477 | ||||||
chr2:44178478
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0008g0020 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-15+9204T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178478 | ||||||
chr2:44178481
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-15+9207T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178481 | ||||||
chr2:44178501
|
C | G | 3 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0343 | 3 | HG03239.hp1 HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15+9227C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178501 | ||||||
chr2:44178514
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+9240C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178514 | ||||||
chr2:44178524
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0314 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-15+9250A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178524 | ||||||
chr2:44178600
|
C | G | 1 | a0001c0001t0002g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-15+9326C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178600 | ||||||
chr2:44178676
|
G | C | 1 | a0001c0001t0001g0337 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-15+9402G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178676 | ||||||
chr2:44178716
|
C | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(171): Show | 176 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.-15+9442C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178716 | ||||||
chr2:44178728
|
C | G | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+9454C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178728 | ||||||
chr2:44178792
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 278 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.-15+9518T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178792 | ||||||
chr2:44178824
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+9550A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178824 | ||||||
chr2:44178854
|
A | C | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(56): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+9580A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178854 | ||||||
chr2:44178856
|
A | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+9582A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178856 | ||||||
chr2:44178922
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+9648A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178922 | ||||||
chr2:44178964
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+9690A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178964 | ||||||
chr2:44179059
|
A | C | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+9785A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179059 | ||||||
chr2:44179073
|
T | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0327others(7): Show | 10 | HG01074.hp2 HG01099.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+9799T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179073 | ||||||
chr2:44179110
|
G | A | 2 | a0001c0001t0007g0218a0001c0001t0007g0219 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-15+9836G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179110 | ||||||
chr2:44179175
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-15+9901A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179175 | ||||||
chr2:44179489
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15+10215T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179489 | ||||||
chr2:44179535
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-15+10261G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179535 | ||||||
chr2:44179537
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15+10263C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179537 | ||||||
chr2:44179547
|
C | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 265 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.-15+10273C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179547 | ||||||
chr2:44179693
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+10419A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179693 | ||||||
chr2:44179774
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-15+10500C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179774 | ||||||
chr2:44179775
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-15+10501G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179775 | ||||||
chr2:44179867
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+10593G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179867 | ||||||
chr2:44179898
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+10624A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179898 | ||||||
chr2:44179901
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0156others(5): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+10627C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179901 | ||||||
chr2:44179902
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0154others(6): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+10628A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179902 | ||||||
chr2:44179907
|
G | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(61): Show | 66 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+10633G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179907 | ||||||
chr2:44179997
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+10723G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179997 | ||||||
chr2:44180009
|
C | CA | 12 | a0001c0001t0001g0207a0001c0001t0001g0221a0001c0001t0001g0222others(9): Show | 12 | HG01106.hp2 HG01952.hp2 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+10754dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44180009 | |||||
chr2:44180009
|
CA | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 88 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-15+10754delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44180009 | |||||
chr2:44180050
|
CT | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(243): Show | 253 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-15+10778delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44180050 | |||||
chr2:44180051
|
T | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-15+10777T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180051 | ||||||
chr2:44180059
|
T | G | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+10785T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180059 | ||||||
chr2:44180225
|
A | T | 1 | a0001c0001t0001g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-15+10951A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180225 | ||||||
chr2:44180466
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+11192C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180466 | ||||||
chr2:44180479
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 265 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.-15+11205G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180479 | ||||||
chr2:44180542
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0217a0001c0001t0001g0330 | 4 | HG02647.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+11268A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180542 | ||||||
chr2:44180597
|
A | G | 2 | a0001c0001t0007g0218a0001c0001t0007g0219 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-15+11323A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180597 | ||||||
chr2:44180641
|
C | G | 1 | a0001c0001t0001g0344 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+11367C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180641 | ||||||
chr2:44180664
|
G | T | 1 | a0001c0001t0002g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15+11390G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180664 | ||||||
chr2:44180846
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 276 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.-15+11572G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180846 | ||||||
chr2:44181026
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-15+11752C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181026 | ||||||
chr2:44181033
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+11759C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181033 | ||||||
chr2:44181103
|
C | G | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-15+11829C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181103 | ||||||
chr2:44181143
|
G | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(256): Show | 266 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-15+11869G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181143 | ||||||
chr2:44181160
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-15+11886A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181160 | ||||||
chr2:44181370
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+12096A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181370 | ||||||
chr2:44181445
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+12171A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181445 | ||||||
chr2:44181448
|
G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 86 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15+12174G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181448 | ||||||
chr2:44181726
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+12452C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181726 | ||||||
chr2:44181731
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+12457A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181731 | ||||||
chr2:44181781
|
C | G | 89 | a0001c0001t0001g0008a0001c0001t0001g0184a0001c0001t0001g0185others(86): Show | 90 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15+12507C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181781 | ||||||
chr2:44181937
|
G | T | 1 | a0001c0001t0002g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-15+12663G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181937 | ||||||
chr2:44182115
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG01069.hp1 HG01081.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-15+12841G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182115 | ||||||
chr2:44182161
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-15+12887T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182161 | ||||||
chr2:44182199
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-15+12925T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182199 | ||||||
chr2:44182353
|
G | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+13079G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182353 | ||||||
chr2:44182466
|
G | A | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+13192G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182466 | ||||||
chr2:44182620
|
G | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15+13346G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182620 | ||||||
chr2:44183056
|
T | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(58): Show | 63 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-15+13782T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183056 | ||||||
chr2:44183094
|
T | A | 178 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 181 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.-15+13820T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183094 | ||||||
chr2:44183246
|
C | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0168others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+13972C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183246 | ||||||
chr2:44183392
|
A | T | 1 | a0001c0001t0002g0186 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-15+14118A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183392 | ||||||
chr2:44183401
|
A | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(69): Show | 74 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-15+14127A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183401 | ||||||
chr2:44183478
|
G | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(53): Show | 58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15+14204G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183478 | ||||||
chr2:44183601
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+14327C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183601 | ||||||
chr2:44183658
|
AG | A | 5 | a0001c0001t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+14385delG | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183658 | ||||||
chr2:44183715
|
C | T | 2 | a0001c0001t0003g0346a0001c0001t0003g0348 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-15+14441C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183715 | ||||||
chr2:44183824
|
C | T | 1 | a0001c0001t0004g0223 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-15+14550C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183824 | ||||||
chr2:44183887
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(56): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+14613C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183887 | ||||||
chr2:44183896
|
C | G | 194 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(191): Show | 197 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-15+14622C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183896 | ||||||
chr2:44183929
|
G | C | 1 | a0001c0001t0002g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-15+14655G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183929 | ||||||
chr2:44183945
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-15+14671A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183945 | ||||||
chr2:44183981
|
G | A | 10 | a0001c0001t0001g0188a0001c0001t0001g0220a0001c0001t0001g0259others(7): Show | 10 | HG01346.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+14707G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183981 | ||||||
chr2:44184086
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+14812T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184086 | ||||||
chr2:44184116
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15+14842T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184116 | ||||||
chr2:44184160
|
A | C | 1 | a0001c0001t0009g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-15+14886A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184160 | ||||||
chr2:44184258
|
A | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0125 | 2 | HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-15+14984A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184258 | ||||||
chr2:44184616
|
A | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(71): Show | 76 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-15+15342A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184616 | ||||||
chr2:44184719
|
T | C | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+15445T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184719 | ||||||
chr2:44184726
|
G | A | 1 | a0001c0001t0003g0347 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-15+15452G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184726 | ||||||
chr2:44184915
|
T | A | 1 | a0001c0001t0001g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-15+15641T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184915 | ||||||
chr2:44184924
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+15650A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184924 | ||||||
chr2:44184935
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15+15661C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184935 | ||||||
chr2:44185161
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-15+15887A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185161 | ||||||
chr2:44185190
|
T | A | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+15916T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185190 | ||||||
chr2:44185259
|
G | T | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14-15927G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185259 | ||||||
chr2:44185453
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-15733C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185453 | ||||||
chr2:44185542
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 79 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-14-15644A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185542 | ||||||
chr2:44185660
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15526A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185660 | ||||||
chr2:44185724
|
TG | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0152others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-15461delG | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185724 | ||||||
chr2:44185725
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 101 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-14-15461G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185725 | ||||||
chr2:44185829
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0141 | 3 | HG01070.hp1 HG01123.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-14-15357C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185829 | ||||||
chr2:44185926
|
G | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-15260G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185926 | ||||||
chr2:44185950
|
T | G | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15236T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185950 | ||||||
chr2:44185994
|
A | G | 2 | a0001c0001t0002g0033a0001c0001t0002g0034 | 2 | HG00741.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-14-15192A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185994 | ||||||
chr2:44186026
|
G | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15160G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186026 | ||||||
chr2:44186027
|
A | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15159A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186027 | ||||||
chr2:44186075
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-14-15111G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186075 | ||||||
chr2:44186336
|
A | T | 1 | a0001c0001t0002g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-14-14850A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186336 | ||||||
chr2:44186523
|
C | T | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG00621.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-14-14663C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186523 | ||||||
chr2:44186561
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-14625G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186561 | ||||||
chr2:44186563
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-14-14623C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186563 | ||||||
chr2:44186575
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-14611A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186575 | ||||||
chr2:44186640
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-14-14546G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186640 | ||||||
chr2:44186685
|
C | G | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(16): Show | 19 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-14-14501C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186685 | ||||||
chr2:44186781
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-14405T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186781 | ||||||
chr2:44186919
|
C | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-14267C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186919 | ||||||
chr2:44186940
|
C | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(28): Show | 33 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-14246C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186940 | ||||||
chr2:44186973
|
T | G | 1 | a0001c0001t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-14-14213T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186973 | ||||||
chr2:44187006
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14-14180A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187006 | ||||||
chr2:44187061
|
A | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(14): Show | 17 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-14125A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187061 | ||||||
chr2:44187113
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-14-14073A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187113 | ||||||
chr2:44187191
|
C | G | 1 | a0001c0001t0002g0186 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-14-13995C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187191 | ||||||
chr2:44187215
|
A | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0192a0001c0001t0001g0193others(11): Show | 15 | HG00642.hp1 HG01099.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-14-13971A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187215 | ||||||
chr2:44187282
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-14-13904A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187282 | ||||||
chr2:44187302
|
A | T | 1 | a0001c0001t0001g0337 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14-13884A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187302 | ||||||
chr2:44187318
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-14-13868A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187318 | ||||||
chr2:44187363
|
T | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-13823T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187363 | ||||||
chr2:44187558
|
G | T | 1 | a0001c0001t0001g0304 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-14-13628G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187558 | ||||||
chr2:44187642
|
C | G | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG00621.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-14-13544C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187642 | ||||||
chr2:44187690
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-13496C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187690 | ||||||
chr2:44187825
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0161others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-13361C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187825 | ||||||
chr2:44187836
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0261 | 2 | HG00673.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-14-13350G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187836 | ||||||
chr2:44187897
|
C | A | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-13289C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187897 | ||||||
chr2:44187911
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-14-13275C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187911 | ||||||
chr2:44187991
|
C | T | 1 | a0001c0001t0002g0186 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-14-13195C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187991 | ||||||
chr2:44188011
|
A | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-13175A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188011 | ||||||
chr2:44188018
|
A | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-14-13168A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188018 | ||||||
chr2:44188247
|
C | G | 1 | a0001c0001t0001g0337 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14-12939C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188247 | ||||||
chr2:44188288
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-12898C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188288 | ||||||
chr2:44188377
|
GTTTC | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0171a0001c0001t0001g0172others(1): Show | 4 | HG02486.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-12793_-14-1279 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188377 | |||||
chr2:44188389
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-12793_-14-1278 others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188389 | |||||
chr2:44188390
|
TTTC | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0168a0001c0001t0001g0169others(9): Show | 12 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-12793_-14-1279 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188390 | |||||
chr2:44188392
|
TC | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0161a0001c0001t0001g0314others(4): Show | 7 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-12793delC | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188392 | ||||||
chr2:44188393
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(16): Show | 21 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14-12793C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188393 | ||||||
chr2:44188393
|
CT | C | 213 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(210): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-14-12773delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188393 | |||||
chr2:44188393
|
CTT | C | 10 | a0001c0001t0001g0178a0001c0001t0001g0189a0001c0001t0001g0227others(7): Show | 10 | HG00639.hp1 HG01070.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-12774_-14-1277 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188393 | |||||
chr2:44188397
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-14-12789T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188397 | ||||||
chr2:44188398
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0002g0066 | 2 | HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-14-12788T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188398 | ||||||
chr2:44188458
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-12728C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188458 | ||||||
chr2:44188478
|
C | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-12708C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188478 | ||||||
chr2:44188493
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-14-12693T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188493 | ||||||
chr2:44188545
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-14-12641C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188545 | ||||||
chr2:44188573
|
C | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0152others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-14-12613C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188573 | ||||||
chr2:44188575
|
T | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 90 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-12611T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188575 | ||||||
chr2:44188577
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-12609C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188577 | ||||||
chr2:44188578
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-12608G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188578 | ||||||
chr2:44188627
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-12559C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188627 | ||||||
chr2:44188713
|
G | GCTTTCCT others(17): Show |
1 | a0001c0001t0001g0036 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-14-12426_-14-1240 others(28): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188713 | |||||
chr2:44188713
|
GCTTTCCT others(17): Show |
G | 2 | a0001c0001t0001g0184a0001c0001t0001g0200 | 2 | HG02523.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-14-12426_-14-1240 others(28): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188713 | |||||
chr2:44188739
|
TTTCC | T | 11 | a0001c0001t0001g0096a0001c0001t0001g0194a0001c0001t0001g0199others(8): Show | 11 | HG01934.hp1 HG01943.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-12427_-14-1242 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188739 | |||||
chr2:44188743
|
CTTCCTTC others(13): Show |
C | 3 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314 | 3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-12423_-14-1240 others(24): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188743 | |||||
chr2:44188763
|
TTTCC | T | 5 | a0001c0001t0001g0230a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-12406_-14-1240 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188763 | |||||
chr2:44188788
|
T | TTCCC | 48 | a0001c0001t0001g0183a0001c0001t0001g0253a0001c0001t0001g0254others(45): Show | 50 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.-14-12393_-14-1239 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188788 | |||||
chr2:44188994
|
G | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(151): Show | 157 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.-14-12192G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188994 | ||||||
chr2:44189053
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-14-12133A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189053 | ||||||
chr2:44189128
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-14-12058T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189128 | ||||||
chr2:44189129
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-14-12057C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189129 | ||||||
chr2:44189142
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-14-12044G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189142 | ||||||
chr2:44189171
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-14-12015C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189171 | ||||||
chr2:44189276
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 91 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.-14-11910A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189276 | ||||||
chr2:44189283
|
C | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314 | 3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-11903C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189283 | ||||||
chr2:44189527
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-11659G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189527 | ||||||
chr2:44189529
|
TCTC | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-11656_-14-1165 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189529 | ||||||
chr2:44189663
|
C | T | 5 | a0001c0001t0001g0230a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-11523C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189663 | ||||||
chr2:44189850
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 89 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.-14-11336T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189850 | ||||||
chr2:44189877
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-11309C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189877 | ||||||
chr2:44189934
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-14-11252A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189934 | ||||||
chr2:44190154
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-11032G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190154 | ||||||
chr2:44190155
|
A | AT | 10 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0124others(7): Show | 10 | HG00639.hp2 HG01943.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-11011dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44190155 | |||||
chr2:44190155
|
AT | A | 208 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(205): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.-14-11011delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44190155 | |||||
chr2:44190155
|
ATT | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0265others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-11012_-14-1101 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44190155 | |||||
chr2:44190161
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-11025T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190161 | ||||||
chr2:44190264
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-14-10922C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190264 | ||||||
chr2:44190268
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0314 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-10918C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190268 | ||||||
chr2:44190294
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-10892A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190294 | ||||||
chr2:44190304
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14-10882G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190304 | ||||||
chr2:44190417
|
C | A | 1 | a0001c0001t0002g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-10769C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190417 | ||||||
chr2:44190438
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-14-10748C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190438 | ||||||
chr2:44190514
|
G | C | 1 | a0001c0001t0001g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-14-10672G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190514 | ||||||
chr2:44190606
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-14-10580T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190606 | ||||||
chr2:44190667
|
C | G | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-14-10519C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190667 | ||||||
chr2:44190786
|
T | G | 1 | a0001c0001t0005g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14-10400T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190786 | ||||||
chr2:44190787
|
G | A | 1 | a0001c0001t0005g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14-10399G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190787 | ||||||
chr2:44190823
|
T | G | 1 | a0001c0001t0005g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14-10363T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190823 | ||||||
chr2:44190826
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-10360G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190826 | ||||||
chr2:44190895
|
C | G | 1 | a0001c0001t0002g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-10291C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190895 | ||||||
chr2:44190953
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0155others(7): Show | 12 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-10233A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190953 | ||||||
chr2:44190993
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-14-10193A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190993 | ||||||
chr2:44191112
|
C | A | 1 | a0001c0001t0002g0077 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-14-10074C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191112 | ||||||
chr2:44191139
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314 | 3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-10047C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191139 | ||||||
chr2:44191157
|
C | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0168others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-10029C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191157 | ||||||
chr2:44191191
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 88 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-14-9995G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191191 | ||||||
chr2:44191245
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-9941G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191245 | ||||||
chr2:44191318
|
A | G | 4 | a0001c0001t0004g0223a0001c0001t0004g0297a0001c0001t0004g0300others(1): Show | 4 | HG01081.hp1 HG01106.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-9868A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191318 | ||||||
chr2:44191669
|
G | C | 1 | a0001c0001t0001g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-14-9517G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191669 | ||||||
chr2:44191721
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-9465A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191721 | ||||||
chr2:44191768
|
T | G | 4 | a0001c0001t0001g0185a0001c0001t0001g0262a0001c0001t0001g0267others(1): Show | 4 | NA18986.hp1 NA18988.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-9418T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191768 | ||||||
chr2:44191791
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-14-9395G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191791 | ||||||
chr2:44191841
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-9345G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191841 | ||||||
chr2:44192017
|
C | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-9169C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192017 | ||||||
chr2:44192049
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-9137C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192049 | ||||||
chr2:44192077
|
C | G | 1 | a0001c0001t0002g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-9109C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192077 | ||||||
chr2:44192165
|
T | G | 1 | a0001c0001t0002g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-14-9021T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192165 | ||||||
chr2:44192185
|
G | GGTATT | 3 | a0001c0001t0001g0180a0001c0001t0003g0345a0001c0001t0003g0347 | 3 | HG01361.hp1 HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-14-9001_-14-9000i others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192185 | ||||||
chr2:44192185
|
G | GGTATTGT others(3): Show |
3 | a0001c0001t0002g0045a0001c0001t0003g0346a0001c0001t0003g0348 | 3 | HG02074.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-14-9001_-14-9000i others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192185 | ||||||
chr2:44192186
|
T | G | 6 | a0001c0001t0001g0180a0001c0001t0002g0045a0001c0001t0003g0345others(3): Show | 6 | HG01361.hp1 HG02055.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-9000T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192186 | ||||||
chr2:44192190
|
G | GGTATT | 115 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(112): Show | 116 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.-14-8954_-14-8950d others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192190
|
G | GGTATTGT others(3): Show |
82 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 88 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-14-8959_-14-8950d others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192190
|
G | GGTATTGT others(8): Show |
23 | a0001c0001t0001g0039a0001c0001t0001g0155a0001c0001t0001g0188others(20): Show | 23 | HG00673.hp2 HG01346.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-8964_-14-8950d others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192190
|
G | GGTATTGT others(13): Show |
3 | a0001c0001t0001g0038a0001c0001t0002g0059a0001c0001t0010g0049 | 3 | HG00099.hp2 HG02683.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-14-8969_-14-8950d others(22): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192190
|
G | GGTATTGT others(18): Show |
2 | a0001c0001t0001g0249a0001c0001t0002g0048 | 2 | NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-14-8974_-14-8950d others(27): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192190
|
G | GTTATGGT others(3): Show |
2 | a0001c0001t0001g0170a0001c0001t0002g0073 | 2 | HG03486.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-14-8996_-14-8995i others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192190 | ||||||
chr2:44192190
|
G | GTTATGGT others(8): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-14-8996_-14-8995i others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192190 | ||||||
chr2:44192190
|
G | T | 6 | a0001c0001t0001g0180a0001c0001t0002g0045a0001c0001t0003g0345others(3): Show | 6 | HG01361.hp1 HG02055.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8996G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192190 | ||||||
chr2:44192190
|
GGTATT | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0096others(50): Show | 55 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-14-8954_-14-8950d others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192190
|
GGTATTGT others(3): Show |
G | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(14): Show | 17 | HG00323.hp1 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-8959_-14-8950d others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192190
|
GGTATTGT others(8): Show |
G | 1 | a0001c0001t0001g0201 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-14-8964_-14-8950d others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | |||||
chr2:44192195
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-8991T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192195 | ||||||
chr2:44192200
|
T | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8986T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192200 | ||||||
chr2:44192234
|
T | TTGTATTG others(7): Show |
1 | a0001c0001t0002g0186 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-14-8950_-14-8949i others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192234 | |||||
chr2:44192277
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-8909G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192277 | ||||||
chr2:44192342
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-8844C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192342 | ||||||
chr2:44192364
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8822A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192364 | ||||||
chr2:44192375
|
C | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0288a0001c0001t0004g0223others(3): Show | 6 | HG01081.hp1 HG01106.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8811C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192375 | ||||||
chr2:44192429
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14-8757T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192429 | ||||||
chr2:44192630
|
C | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(15): Show | 19 | HG00621.hp1 NA18945.hp2 NA18950.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-8556C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192630 | ||||||
chr2:44192722
|
G | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8464G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192722 | ||||||
chr2:44192852
|
A | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314 | 3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-8334A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192852 | ||||||
chr2:44192852
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-14-8334A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192852 | ||||||
chr2:44192923
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-14-8263A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192923 | ||||||
chr2:44192928
|
A | T | 1 | a0001c0001t0001g0334 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-14-8258A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192928 | ||||||
chr2:44192960
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14-8226C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192960 | ||||||
chr2:44193023
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-8163G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193023 | ||||||
chr2:44193135
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0180a0001c0001t0001g0182 | 4 | HG00733.hp2 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8051A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193135 | ||||||
chr2:44193155
|
A | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8031A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193155 | ||||||
chr2:44193272
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314 | 3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-7914T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193272 | ||||||
chr2:44193351
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-7835A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193351 | ||||||
chr2:44193384
|
CCTCTGAA others(42): Show |
C | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-7796_-14-7748d others(51): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193384 | |||||
chr2:44193575
|
C | CT | 13 | a0001c0001t0001g0096a0001c0001t0001g0185a0001c0001t0001g0249others(10): Show | 13 | HG00621.hp2 HG01358.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-7591dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193575 | |||||
chr2:44193575
|
CT | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 47 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.-14-7591delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193575 | |||||
chr2:44193575
|
CTT | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(49): Show | 54 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-14-7592_-14-7591d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193575 | |||||
chr2:44193636
|
G | C | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-7550G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193636 | ||||||
chr2:44193639
|
C | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 88 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-14-7547C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193639 | ||||||
chr2:44193740
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0161others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-7446G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193740 | ||||||
chr2:44193885
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-7301A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193885 | ||||||
chr2:44193933
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-7253C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193933 | ||||||
chr2:44193939
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314 | 3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-7247A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193939 | ||||||
chr2:44194028
|
A | G | 2 | a0001c0001t0007g0218a0001c0001t0007g0219 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-14-7158A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194028 | ||||||
chr2:44194129
|
T | C | 1 | a0001c0001t0003g0347 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-14-7057T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194129 | ||||||
chr2:44194324
|
T | C | 7 | a0001c0001t0001g0228a0001c0001t0001g0233a0001c0001t0001g0234others(4): Show | 7 | NA18949.hp1 NA18969.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-6862T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194324 | ||||||
chr2:44194351
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0096 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-14-6835C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194351 | ||||||
chr2:44194403
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0161others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-6783T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194403 | ||||||
chr2:44194489
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-6697C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194489 | ||||||
chr2:44194596
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 85 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-14-6590G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194596 | ||||||
chr2:44194756
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-14-6430A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194756 | ||||||
chr2:44194807
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-6379G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194807 | ||||||
chr2:44194853
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-6333A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194853 | ||||||
chr2:44194882
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 96 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.-14-6304G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194882 | ||||||
chr2:44194898
|
C | CT | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 103 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.-14-6270dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44194898 | |||||
chr2:44194959
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-14-6227C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194959 | ||||||
chr2:44194963
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0320 | 2 | HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-14-6223A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194963 | ||||||
chr2:44194972
|
G | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 273 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.-14-6214G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194972 | ||||||
chr2:44195027
|
G | T | 1 | a0001c0001t0003g0345 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-14-6159G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195027 | ||||||
chr2:44195036
|
C | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-6150C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195036 | ||||||
chr2:44195100
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0161others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-6086C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195100 | ||||||
chr2:44195112
|
C | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-14-6074C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195112 | ||||||
chr2:44195140
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-6046G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195140 | ||||||
chr2:44195205
|
C | CT | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 94 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-14-5968dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44195205 | |||||
chr2:44195232
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-14-5954C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195232 | ||||||
chr2:44195323
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-14-5863C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195323 | ||||||
chr2:44195364
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-14-5822A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195364 | ||||||
chr2:44195455
|
C | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(59): Show | 64 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-14-5731C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195455 | ||||||
chr2:44195470
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-14-5716C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195470 | ||||||
chr2:44195620
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-5566T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195620 | ||||||
chr2:44195721
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 81 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-14-5465C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195721 | ||||||
chr2:44195788
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-5398C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195788 | ||||||
chr2:44195852
|
A | T | 1 | a0001c0001t0001g0318 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-5334A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195852 | ||||||
chr2:44195946
|
A | T | 1 | a0001c0001t0001g0318 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-5240A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195946 | ||||||
chr2:44196094
|
T | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-5092T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196094 | ||||||
chr2:44196175
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-14-5011C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196175 | ||||||
chr2:44196401
|
G | A | 4 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG02622.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-4785G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196401 | ||||||
chr2:44196419
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0175 | 2 | HG01109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-14-4767C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196419 | ||||||
chr2:44196464
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14-4722T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196464 | ||||||
chr2:44196675
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-4511C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196675 | ||||||
chr2:44196832
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-4354G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196832 | ||||||
chr2:44196837
|
A | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-4349A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196837 | ||||||
chr2:44197039
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-14-4147A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197039 | ||||||
chr2:44197051
|
T | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(14): Show | 17 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-4135T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197051 | ||||||
chr2:44197123
|
C | CT | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-4054dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44197123 | |||||
chr2:44197169
|
G | A | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-4017G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197169 | ||||||
chr2:44197204
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-14-3982T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197204 | ||||||
chr2:44197361
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-14-3825C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197361 | ||||||
chr2:44197378
|
C | G | 1 | a0001c0001t0001g0349 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-14-3808C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197378 | ||||||
chr2:44197798
|
T | C | 1 | a0001c0001t0001g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-14-3388T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197798 | ||||||
chr2:44197837
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14-3349G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197837 | ||||||
chr2:44197923
|
G | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-3263G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197923 | ||||||
chr2:44197955
|
C | G | 1 | a0001c0001t0001g0333 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-14-3231C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197955 | ||||||
chr2:44197964
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-14-3222A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197964 | ||||||
chr2:44198004
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3182C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198004 | ||||||
chr2:44198284
|
C | T | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-14-2902C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198284 | ||||||
chr2:44198369
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-2817C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198369 | ||||||
chr2:44198407
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2779C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198407 | ||||||
chr2:44198450
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-14-2736C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198450 | ||||||
chr2:44198777
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-14-2409A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198777 | ||||||
chr2:44198837
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2349A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198837 | ||||||
chr2:44198975
|
A | C | 344 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(350): Show |
intron_variant | MODIFIER | c.-14-2211A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198975 | ||||||
chr2:44199071
|
A | C | 1 | a0001c0001t0001g0317 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-14-2115A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199071 | ||||||
chr2:44199149
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2037C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199149 | ||||||
chr2:44199150
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0108 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-2036C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199150 | ||||||
chr2:44199151
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2035G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199151 | ||||||
chr2:44199170
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 94 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-14-2016G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199170 | ||||||
chr2:44199244
|
C | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0259a0001c0001t0001g0315 | 3 | HG01346.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-14-1942C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199244 | ||||||
chr2:44199257
|
C | CA | 9 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-1917dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199257 | |||||
chr2:44199274
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-14-1912C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199274 | ||||||
chr2:44199303
|
C | CA | 8 | a0001c0001t0001g0031a0001c0001t0001g0171a0001c0001t0001g0206others(5): Show | 8 | HG02559.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-1869dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199303 | |||||
chr2:44199311
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-14-1875A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199311 | ||||||
chr2:44199311
|
AAAAAAAT others(6): Show |
A | 16 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0111others(13): Show | 18 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14-1868_-14-1856d others(15): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199311 | |||||
chr2:44199312
|
A | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0326 | 2 | NA18999.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-14-1874A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199312 | ||||||
chr2:44199312
|
AAAAAATA others(5): Show |
A | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(51): Show | 56 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14-1868_-14-1857d others(14): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199312 | |||||
chr2:44199313
|
AAAAATAA others(4): Show |
A | 7 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0113others(4): Show | 7 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1868_-14-1858d others(13): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199313 | |||||
chr2:44199314
|
A | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0234 | 2 | NA18969.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-14-1872A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199314 | ||||||
chr2:44199317
|
AT | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | NA18949.hp1 NA18969.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1868delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199317 | ||||||
chr2:44199318
|
T | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0171others(6): Show | 9 | HG01934.hp1 HG01943.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-1868T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199318 | ||||||
chr2:44199324
|
T | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(30): Show | 34 | HG00323.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-1862T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199324 | ||||||
chr2:44199324
|
T | TA | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-1848dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199324 | |||||
chr2:44199325
|
A | T | 1 | a0001c0001t0002g0063 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-1861A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199325 | ||||||
chr2:44199327
|
A | AT | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0091others(4): Show | 7 | HG01074.hp2 HG01099.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-1859_-14-1858i others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199327 | ||||||
chr2:44199327
|
A | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-1859A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199327 | ||||||
chr2:44199330
|
A | T | 7 | a0001c0001t0001g0096a0001c0001t0001g0177a0001c0001t0001g0187others(4): Show | 7 | HG00438.hp1 NA18953.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1856A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199330 | ||||||
chr2:44199331
|
A | AT | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1855_-14-1854i others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199331 | ||||||
chr2:44199335
|
A | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-1851A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199335 | ||||||
chr2:44199350
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-14-1836A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199350 | ||||||
chr2:44199430
|
A | G | 344 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(350): Show |
intron_variant | MODIFIER | c.-14-1756A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199430 | ||||||
chr2:44199712
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-1474A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199712 | ||||||
chr2:44199855
|
T | C | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1331T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199855 | ||||||
chr2:44199899
|
C | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 95 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-14-1287C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199899 | ||||||
chr2:44199943
|
A | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(12): Show | 15 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-1243A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199943 | ||||||
chr2:44199994
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-14-1192C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199994 | ||||||
chr2:44200053
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-14-1133C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200053 | ||||||
chr2:44200148
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-14-1038T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200148 | ||||||
chr2:44200265
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-14-921T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200265 | ||||||
chr2:44200405
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0008g0020 | 2 | HG00323.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-781A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200405 | ||||||
chr2:44200540
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-646A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200540 | ||||||
chr2:44200628
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-558T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200628 | ||||||
chr2:44200800
|
C | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-386C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200800 | ||||||
chr2:44200808
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-14-378A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200808 | ||||||
chr2:44200880
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-306A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200880 | ||||||
chr2:44200930
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-256T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200930 | ||||||
chr2:44200956
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-230C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200956 | ||||||
chr2:44201065
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-14-121C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201065 | ||||||
chr2:44201096
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-14-90T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201096 | ||||||
chr2:44201103
|
G | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0168others(13): Show | 16 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-83G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201103 | ||||||
chr2:44201144
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-14-42C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201144 | ||||||
chr2:44202135
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+90T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44202135 | ||||||
chr2:44202222
|
C | T | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG02040.hp1 HG02083.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.846+177C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44202222 | ||||||
chr2:44202604
|
C | CTATG | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.846+561_846+562ins others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44202604 | |||||
chr2:44203096
|
A | T | 1 | a0001c0001t0002g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.846+1051A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203096 | ||||||
chr2:44203099
|
T | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0152others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.846+1054T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203099 | ||||||
chr2:44203120
|
A | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.846+1075A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203120 | ||||||
chr2:44203166
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+1121C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203166 | ||||||
chr2:44203473
|
T | TA | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 168 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.846+1436dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44203473 | |||||
chr2:44203528
|
A | G | 1 | a0001c0001t0001g0005 | 2 | NA18945.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.846+1483A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203528 | ||||||
chr2:44203630
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 98 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.846+1585A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203630 | ||||||
chr2:44203676
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.846+1631C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203676 | ||||||
chr2:44203710
|
G | A | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(57): Show | 62 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.846+1665G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203710 | ||||||
chr2:44203850
|
C | A | 1 | a0001c0001t0002g0055 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.846+1805C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203850 | ||||||
chr2:44204011
|
C | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.846+1966C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204011 | ||||||
chr2:44204092
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.846+2047C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204092 | ||||||
chr2:44204316
|
T | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.846+2271T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204316 | ||||||
chr2:44204316
|
T | G | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.846+2271T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204316 | ||||||
chr2:44204517
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.846+2472A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204517 | ||||||
chr2:44204535
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+2490G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204535 | ||||||
chr2:44204573
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.846+2528C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204573 | ||||||
chr2:44204580
|
A | G | 73 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(70): Show | 75 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.846+2535A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204580 | ||||||
chr2:44204661
|
A | G | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2616A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204661 | ||||||
chr2:44204732
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0156others(5): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+2687G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204732 | ||||||
chr2:44204783
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.846+2738C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204783 | ||||||
chr2:44204816
|
G | A | 163 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 166 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.846+2771G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204816 | ||||||
chr2:44204856
|
C | G | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2811C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204856 | ||||||
chr2:44204858
|
C | CA | 39 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0037others(36): Show | 40 | HG00609.hp1 HG00642.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.846+2839dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | |||||
chr2:44204858
|
C | CAA | 13 | a0001c0001t0001g0008a0001c0001t0001g0192a0001c0001t0001g0193others(10): Show | 14 | HG00642.hp1 HG01099.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.846+2838_846+2839d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | |||||
chr2:44204858
|
CA | C | 13 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0138others(10): Show | 13 | HG00544.hp1 HG01109.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.846+2839delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | |||||
chr2:44204858
|
CAA | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0314a0001c0001t0003g0345others(7): Show | 10 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+2838_846+2839d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | |||||
chr2:44204858
|
CAAAAAAA | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(6): Show | 9 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.846+2833_846+2839d others(9): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | |||||
chr2:44204858
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.846+2830_846+2839d others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | |||||
chr2:44204858
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.846+2827_846+2839d others(15): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | |||||
chr2:44205142
|
G | C | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(2): Show | 5 | HG01074.hp2 HG01099.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.846+3097G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205142 | ||||||
chr2:44205332
|
AGTGGGT | A | 151 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(148): Show | 154 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.846+3309_846+3314d others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205332 | |||||
chr2:44205336
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.846+3291G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205336 | ||||||
chr2:44205337
|
G | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 99 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.846+3292G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205337 | ||||||
chr2:44205348
|
G | GGTGTGTG others(15): Show |
1 | a0001c0001t0001g0149 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.846+3308_846+3309i others(24): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205348 | |||||
chr2:44205350
|
TGTGG | T | 13 | a0001c0001t0001g0177a0001c0001t0001g0203a0001c0001t0001g0206others(10): Show | 13 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.846+3309_846+3312d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205350 | |||||
chr2:44205354
|
G | GGTGTGTG others(11): Show |
1 | a0001c0001t0001g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.846+3319_846+3320i others(20): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(13): Show |
8 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0027others(5): Show | 8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(22): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(15): Show |
2 | a0001c0001t0001g0096a0001c0001t0003g0030 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.846+3319_846+3320i others(24): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(17): Show |
3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0008g0020 | 3 | HG02809.hp1 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.846+3319_846+3320i others(26): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(19): Show |
18 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0127others(15): Show | 18 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(28): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(21): Show |
56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(53): Show | 58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(30): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(23): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0121others(7): Show | 12 | HG01106.hp1 HG02015.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(32): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(25): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0138 | 2 | HG02922.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.846+3319_846+3320i others(34): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(27): Show |
4 | a0001c0001t0001g0123a0001c0001t0001g0158a0001c0001t0001g0166others(1): Show | 4 | HG02280.hp2 HG02486.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(36): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(24): Show |
1 | a0001c0001t0001g0140 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.846+3319_846+3320i others(33): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | GGTGTGTG others(24): Show |
1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.846+3319_846+3320i others(33): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | |||||
chr2:44205354
|
G | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0284a0001c0001t0001g0295others(1): Show | 4 | HG01934.hp2 HG02015.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+3309G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205354 | ||||||
chr2:44205356
|
T | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0221a0001c0001t0001g0242others(2): Show | 6 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+3311T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205356 | ||||||
chr2:44205374
|
T | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0004c0003t0001g0013 | 3 | HG02559.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.846+3329T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205374 | ||||||
chr2:44205380
|
T | TAA | 4 | a0001c0001t0001g0152a0001c0001t0003g0030a0001c0001t0006g0151others(1): Show | 4 | HG01884.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+3336_846+3337d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205380 | |||||
chr2:44205523
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.846+3478C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205523 | ||||||
chr2:44205630
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0112 | 2 | HG01070.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.847-3580A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205630 | ||||||
chr2:44205713
|
A | G | 1 | a0001c0001t0001g0284 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.847-3497A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205713 | ||||||
chr2:44205769
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.847-3441A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205769 | ||||||
chr2:44205860
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.847-3350C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205860 | ||||||
chr2:44205986
|
A | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(59): Show | 64 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.847-3224A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205986 | ||||||
chr2:44206044
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-3166A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206044 | ||||||
chr2:44206259
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847-2951A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206259 | ||||||
chr2:44206564
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.847-2646C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206564 | ||||||
chr2:44206572
|
G | A | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-2638G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206572 | ||||||
chr2:44206638
|
TTAAAAGA others(11): Show |
T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.847-2565_847-2548d others(20): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44206638 | |||||
chr2:44206656
|
C | G | 67 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(64): Show | 69 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.847-2554C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206656 | ||||||
chr2:44206688
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.847-2522A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206688 | ||||||
chr2:44206726
|
T | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2484T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206726 | ||||||
chr2:44206728
|
T | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2482T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206728 | ||||||
chr2:44206730
|
T | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2480T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206730 | ||||||
chr2:44206731
|
T | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2479T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206731 | ||||||
chr2:44206732
|
G | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2478G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206732 | ||||||
chr2:44206733
|
T | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2477T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206733 | ||||||
chr2:44206735
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2475G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206735 | ||||||
chr2:44206736
|
T | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2474T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206736 | ||||||
chr2:44206737
|
T | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0247 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2473T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206737 | ||||||
chr2:44206776
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.847-2434A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206776 | ||||||
chr2:44206855
|
A | G | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-2355A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206855 | ||||||
chr2:44206867
|
C | G | 1 | a0001c0001t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.847-2343C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206867 | ||||||
chr2:44207078
|
A | G | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.847-2132A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207078 | ||||||
chr2:44207145
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.847-2065C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207145 | ||||||
chr2:44207166
|
AC | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.847-2043delC | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207166 | ||||||
chr2:44207190
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.847-2020G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207190 | ||||||
chr2:44207329
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.847-1881G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207329 | ||||||
chr2:44207493
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.847-1717G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207493 | ||||||
chr2:44207579
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.847-1631G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207579 | ||||||
chr2:44207635
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0220 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.847-1575G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207635 | ||||||
chr2:44207639
|
C | T | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.847-1571C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207639 | ||||||
chr2:44207669
|
A | C | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.847-1541A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207669 | ||||||
chr2:44207888
|
C | CT | 26 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(23): Show | 26 | HG01169.hp1 HG01258.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.847-1303dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44207888 | |||||
chr2:44207888
|
CT | C | 149 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(146): Show | 152 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.847-1303delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44207888 | |||||
chr2:44207973
|
C | T | 8 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0055others(5): Show | 10 | HG00733.hp1 NA18953.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.847-1237C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207973 | ||||||
chr2:44208041
|
A | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-1169A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208041 | ||||||
chr2:44208121
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-1089C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208121 | ||||||
chr2:44208150
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-1060A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208150 | ||||||
chr2:44208186
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 119 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.847-1024T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208186 | ||||||
chr2:44208384
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-826C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208384 | ||||||
chr2:44208386
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-824C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208386 | ||||||
chr2:44208544
|
C | G | 166 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 169 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.847-666C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208544 | ||||||
chr2:44208572
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-638G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208572 | ||||||
chr2:44208583
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.847-627G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208583 | ||||||
chr2:44208669
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0109a0001c0001t0001g0140 | 4 | HG00642.hp2 HG01981.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-541C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208669 | ||||||
chr2:44208868
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.847-342A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208868 | ||||||
chr2:44208874
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.847-336G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208874 | ||||||
chr2:44209180
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.847-30T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44209180 | ||||||
chr2:44209188
|
C | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-22C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44209188 | ||||||
chr2:44209431
|
C | CAA | 11 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0096others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.964+116_964+117dup others(2): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209431 | |||||
chr2:44209456
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964+129A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209456 | ||||||
chr2:44209518
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.964+191A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209518 | ||||||
chr2:44209604
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.964+277C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209604 | ||||||
chr2:44209629
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.964+302T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209629 | ||||||
chr2:44209632
|
C | G | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+305C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209632 | ||||||
chr2:44209777
|
C | CA | 31 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0017others(28): Show | 32 | HG00438.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.964+468dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209777 | |||||
chr2:44209777
|
CA | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 101 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.964+468delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209777 | |||||
chr2:44209833
|
GA | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 7 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+512delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209833 | |||||
chr2:44209874
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.964+547C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209874 | ||||||
chr2:44210078
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 112 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.964+751G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210078 | ||||||
chr2:44210101
|
G | C | 1 | a0001c0001t0003g0345 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.964+774G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210101 | ||||||
chr2:44210127
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+800C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210127 | ||||||
chr2:44210161
|
T | G | 1 | a0001c0001t0001g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.964+834T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210161 | ||||||
chr2:44210170
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0004c0003t0001g0013 | 3 | HG02559.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.964+843C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210170 | ||||||
chr2:44210172
|
A | G | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+845A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210172 | ||||||
chr2:44210215
|
A | AT | 11 | a0001c0001t0001g0185a0001c0001t0001g0262a0001c0001t0001g0267others(8): Show | 11 | HG01358.hp1 HG01975.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.964+907dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44210215 | |||||
chr2:44210215
|
AT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 116 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.964+907delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44210215 | |||||
chr2:44210339
|
C | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+1012C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210339 | ||||||
chr2:44210458
|
A | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.964+1131A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210458 | ||||||
chr2:44210802
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.964+1475C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210802 | ||||||
chr2:44210858
|
C | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.964+1531C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210858 | ||||||
chr2:44210931
|
T | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+1604T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210931 | ||||||
chr2:44210968
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964+1641T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210968 | ||||||
chr2:44210973
|
T | G | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.964+1646T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210973 | ||||||
chr2:44211002
|
G | C | 8 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 8 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+1675G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211002 | ||||||
chr2:44211029
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0220 | 3 | HG02486.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.964+1702C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211029 | ||||||
chr2:44211034
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.964+1707G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211034 | ||||||
chr2:44211107
|
G | T | 158 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(155): Show | 161 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.964+1780G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211107 | ||||||
chr2:44211114
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.964+1787T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211114 | ||||||
chr2:44211169
|
A | G | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+1842A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211169 | ||||||
chr2:44211464
|
T | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.964+2137T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211464 | ||||||
chr2:44211485
|
T | C | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.964+2158T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211485 | ||||||
chr2:44211589
|
AAT | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 167 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.964+2265_964+2266d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44211589 | |||||
chr2:44211742
|
CT | C | 219 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.964+2439delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44211742 | |||||
chr2:44211742
|
CTT | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 107 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.964+2438_964+2439d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44211742 | |||||
chr2:44211792
|
C | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2465C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211792 | ||||||
chr2:44211827
|
G | A | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+2500G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211827 | ||||||
chr2:44211836
|
G | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+2509G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211836 | ||||||
chr2:44211993
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.964+2666G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211993 | ||||||
chr2:44212084
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(56): Show | 61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.964+2757G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212084 | ||||||
chr2:44212205
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.964+2878C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212205 | ||||||
chr2:44212333
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.964+3006C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212333 | ||||||
chr2:44212361
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.964+3034C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212361 | ||||||
chr2:44212516
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.964+3189C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212516 | ||||||
chr2:44212586
|
G | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+3259G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212586 | ||||||
chr2:44212628
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.964+3301A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212628 | ||||||
chr2:44212721
|
G | A | 342 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(339): Show | 351 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(348): Show |
intron_variant | MODIFIER | c.964+3394G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212721 | ||||||
chr2:44212749
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0154others(6): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.964+3422G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212749 | ||||||
chr2:44212773
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 75 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.964+3446G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212773 | ||||||
chr2:44212781
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.964+3454C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212781 | ||||||
chr2:44212872
|
G | T | 1 | a0002c0002t0001g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.964+3545G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212872 | ||||||
chr2:44212894
|
T | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 158 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.964+3567T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212894 | ||||||
chr2:44212896
|
C | T | 9 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(6): Show | 9 | HG00408.hp2 NA18980.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.964+3569C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212896 | ||||||
chr2:44212978
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.964+3651A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212978 | ||||||
chr2:44212991
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.964+3664C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212991 | ||||||
chr2:44213013
|
C | CA | 25 | a0001c0001t0001g0039a0001c0001t0001g0102a0001c0001t0001g0120others(22): Show | 25 | HG00597.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.964+3706dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213013 | |||||
chr2:44213013
|
CA | C | 22 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(19): Show | 22 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.964+3706delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213013 | |||||
chr2:44213104
|
C | CT | 15 | a0001c0001t0001g0037a0001c0001t0001g0161a0001c0001t0001g0162others(12): Show | 15 | HG00323.hp1 HG00438.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.964+3794dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213104 | |||||
chr2:44213104
|
CT | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 82 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.964+3794delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213104 | |||||
chr2:44213382
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.964+4055C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213382 | ||||||
chr2:44213398
|
A | T | 1 | a0001c0001t0003g0347 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.964+4071A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213398 | ||||||
chr2:44213405
|
C | T | 340 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(337): Show | 349 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.964+4078C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213405 | ||||||
chr2:44213480
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.964+4153T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213480 | ||||||
chr2:44213499
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.964+4172A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213499 | ||||||
chr2:44213714
|
T | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(338): Show | 350 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(347): Show |
intron_variant | MODIFIER | c.965-4253T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213714 | ||||||
chr2:44213889
|
ATAGTT | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-4075_965-4071d others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213889 | |||||
chr2:44213921
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.965-4046A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213921 | ||||||
chr2:44213954
|
G | A | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-4013G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213954 | ||||||
chr2:44214013
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.965-3954T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214013 | ||||||
chr2:44214039
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-3928C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214039 | ||||||
chr2:44214140
|
C | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0262a0001c0001t0001g0267others(2): Show | 5 | NA18944.hp1 NA18986.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-3827C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214140 | ||||||
chr2:44214149
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.965-3818G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214149 | ||||||
chr2:44214169
|
G | A | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.965-3798G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214169 | ||||||
chr2:44214270
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-3697G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214270 | ||||||
chr2:44214320
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-3647C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214320 | ||||||
chr2:44214378
|
T | G | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-3589T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214378 | ||||||
chr2:44214410
|
A | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.965-3557A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214410 | ||||||
chr2:44214525
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0008g0020 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.965-3442A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214525 | ||||||
chr2:44214558
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171 | 3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.965-3409G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214558 | ||||||
chr2:44214643
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.965-3324G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214643 | ||||||
chr2:44214704
|
C | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.965-3263C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214704 | ||||||
chr2:44214722
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-3245G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214722 | ||||||
chr2:44214868
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.965-3099T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214868 | ||||||
chr2:44214961
|
G | A | 18 | a0001c0001t0001g0185a0001c0001t0001g0197a0001c0001t0001g0203others(15): Show | 18 | HG00597.hp1 HG01167.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.965-3006G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214961 | ||||||
chr2:44215008
|
G | A | 9 | a0001c0001t0001g0185a0001c0001t0001g0262a0001c0001t0001g0267others(6): Show | 9 | HG02015.hp2 HG02040.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-2959G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215008 | ||||||
chr2:44215104
|
G | C | 5 | a0001c0001t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-2863G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215104 | ||||||
chr2:44215187
|
T | TA | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-2776dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44215187 | |||||
chr2:44215373
|
A | G | 1 | a0001c0001t0001g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.965-2594A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215373 | ||||||
chr2:44215383
|
A | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2584A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215383 | ||||||
chr2:44215418
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2549A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215418 | ||||||
chr2:44215420
|
T | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2547T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215420 | ||||||
chr2:44215461
|
G | GA | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(11): Show | 14 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.965-2494dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44215461 | |||||
chr2:44215617
|
T | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-2350T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215617 | ||||||
chr2:44215828
|
G | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2139G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215828 | ||||||
chr2:44215929
|
C | A | 1 | a0001c0001t0002g0097 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.965-2038C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215929 | ||||||
chr2:44215940
|
C | G | 342 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(339): Show | 351 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(348): Show |
intron_variant | MODIFIER | c.965-2027C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215940 | ||||||
chr2:44216040
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.965-1927A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216040 | ||||||
chr2:44216216
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-1751A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216216 | ||||||
chr2:44216240
|
G | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-1727G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216240 | ||||||
chr2:44216388
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.965-1579C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216388 | ||||||
chr2:44216449
|
C | T | 5 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-1518C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216449 | ||||||
chr2:44216717
|
G | C | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-1250G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216717 | ||||||
chr2:44216728
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.965-1239C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216728 | ||||||
chr2:44216837
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-1130A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216837 | ||||||
chr2:44216902
|
C | CA | 171 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 174 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.965-1052dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44216902 | |||||
chr2:44216902
|
C | CAA | 9 | a0001c0001t0001g0011a0001c0001t0001g0185a0001c0001t0001g0262others(6): Show | 9 | HG01358.hp1 HG03704.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-1053_965-1052d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44216902 | |||||
chr2:44216933
|
G | C | 1 | a0001c0001t0001g0165 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.965-1034G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216933 | ||||||
chr2:44216967
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.965-1000C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216967 | ||||||
chr2:44216971
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.965-996C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216971 | ||||||
chr2:44217025
|
G | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0152others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-942G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217025 | ||||||
chr2:44217058
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0205 | 2 | NA18964.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.965-909G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217058 | ||||||
chr2:44217068
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.965-899G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217068 | ||||||
chr2:44217068
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.965-899G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217068 | ||||||
chr2:44217148
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-819C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217148 | ||||||
chr2:44217264
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.965-703T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217264 | ||||||
chr2:44217350
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.965-617G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217350 | ||||||
chr2:44217380
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.965-587C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217380 | ||||||
chr2:44217399
|
C | CA | 28 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(25): Show | 28 | HG00735.hp2 HG01243.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.965-553dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44217399 | |||||
chr2:44217414
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.965-553A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217414 | ||||||
chr2:44217468
|
A | G | 9 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(6): Show | 9 | HG00408.hp2 NA18980.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-499A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217468 | ||||||
chr2:44217568
|
C | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.965-399C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217568 | ||||||
chr2:44217620
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-347G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217620 | ||||||
chr2:44217686
|
T | A | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-281T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217686 | ||||||
chr2:44217778
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.965-189C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217778 | ||||||
chr2:44217861
|
T | A | 2 | a0001c0001t0001g0158a0001c0001t0008g0020 | 2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.965-106T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217861 | ||||||
chr2:44217902
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.965-65T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217902 | ||||||
chr2:44218096
|
C | G | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1076+18C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 4/5 | chr2 | 44218096 | ||||||
chr2:44218465
|
GT | G | 6 | a0001c0001t0001g0270a0001c0001t0001g0287a0001c0001t0001g0336others(3): Show | 6 | HG03017.hp1 HG03239.hp1 HG03942.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1077-3delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 44218465 | |||||
chr2:44218547
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0154others(8): Show | 13 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1134+10A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44218547 | ||||||
chr2:44218711
|
A | ACTTC | 5 | a0001c0001t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+174_1134+175i others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44218711 | ||||||
chr2:44219068
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1134+531A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219068 | ||||||
chr2:44219084
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1134+547A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219084 | ||||||
chr2:44219198
|
C | CT | 9 | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0001g0222others(6): Show | 9 | HG01106.hp2 HG01517.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1134+674dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44219198 | |||||
chr2:44219230
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+693A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219230 | ||||||
chr2:44219353
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 285 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1134+816T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219353 | ||||||
chr2:44219396
|
A | T | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1134+859A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219396 | ||||||
chr2:44219424
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1134+887A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219424 | ||||||
chr2:44219640
|
G | A | 345 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(351): Show |
intron_variant | MODIFIER | c.1134+1103G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219640 | ||||||
chr2:44219792
|
T | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 283 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.1134+1255T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219792 | ||||||
chr2:44219835
|
C | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+1298C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219835 | ||||||
chr2:44219930
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1134+1393C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219930 | ||||||
chr2:44220054
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1134+1517T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220054 | ||||||
chr2:44220101
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+1564T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220101 | ||||||
chr2:44220104
|
C | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+1567C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220104 | ||||||
chr2:44220158
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1134+1621A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220158 | ||||||
chr2:44220190
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0147 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1134+1653A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220190 | ||||||
chr2:44220237
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1134+1700A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220237 | ||||||
chr2:44220263
|
C | CAT | 56 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(53): Show | 58 | HG00408.hp2 HG00544.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1134+1744_1134+174 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | |||||
chr2:44220263
|
C | CATAT | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(72): Show | 78 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1134+1742_1134+174 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | |||||
chr2:44220263
|
C | CATATAT | 4 | a0001c0001t0001g0004a0001c0001t0001g0109a0001c0001t0001g0140others(1): Show | 5 | HG00642.hp2 HG01981.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+1740_1134+174 others(10): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | |||||
chr2:44220263
|
C | CATATATA others(1): Show |
9 | a0001c0001t0001g0023a0001c0001t0001g0145a0001c0001t0001g0152others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1134+1738_1134+174 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | |||||
chr2:44220263
|
C | CATATATA others(3): Show |
6 | a0001c0001t0001g0009a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+1736_1134+174 others(14): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | |||||
chr2:44220263
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1134+1734_1134+174 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | |||||
chr2:44220371
|
T | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0152others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+1834T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220371 | ||||||
chr2:44220430
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1134+1893C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220430 | ||||||
chr2:44220659
|
G | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1134+2122G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220659 | ||||||
chr2:44220687
|
A | C | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 175 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1134+2150A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220687 | ||||||
chr2:44220722
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1134+2185A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220722 | ||||||
chr2:44220786
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1134+2249T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220786 | ||||||
chr2:44220824
|
T | G | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 175 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1134+2287T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220824 | ||||||
chr2:44220856
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1134+2319C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220856 | ||||||
chr2:44221042
|
T | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+2505T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221042 | ||||||
chr2:44221252
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1134+2715T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221252 | ||||||
chr2:44221362
|
C | T | 2 | a0001c0001t0001g0332a0001c0001t0001g0334 | 2 | HG02523.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1134+2825C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221362 | ||||||
chr2:44221493
|
G | A | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 262 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1134+2956G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221493 | ||||||
chr2:44221515
|
G | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0041 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1134+2978G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221515 | ||||||
chr2:44221540
|
G | C | 1 | a0001c0001t0001g0314 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1134+3003G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221540 | ||||||
chr2:44221596
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+3059A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221596 | ||||||
chr2:44221618
|
A | G | 1 | a0001c0001t0001g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1134+3081A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221618 | ||||||
chr2:44221625
|
A | T | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1134+3088A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221625 | ||||||
chr2:44221917
|
C | G | 9 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0257others(6): Show | 9 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1134+3380C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221917 | ||||||
chr2:44221942
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1134+3405C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221942 | ||||||
chr2:44222007
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 109 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1134+3470G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222007 | ||||||
chr2:44222014
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1134+3477C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222014 | ||||||
chr2:44222048
|
C | T | 5 | a0001c0001t0001g0270a0001c0001t0001g0336a0001c0001t0001g0337others(2): Show | 5 | HG03017.hp1 HG03239.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+3511C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222048 | ||||||
chr2:44222121
|
G | A | 2 | a0001c0001t0001g0321a0001c0001t0001g0322 | 2 | NA18968.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1134+3584G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222121 | ||||||
chr2:44222201
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0288 | 2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1134+3664G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222201 | ||||||
chr2:44222458
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1134+3921A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222458 | ||||||
chr2:44222525
|
C | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+3988C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222525 | ||||||
chr2:44222551
|
C | T | 151 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(148): Show | 154 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1134+4014C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222551 | ||||||
chr2:44222573
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1134+4036C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222573 | ||||||
chr2:44222606
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1134+4069C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222606 | ||||||
chr2:44222642
|
G | C | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1134+4105G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222642 | ||||||
chr2:44222882
|
G | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+4345G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222882 | ||||||
chr2:44223111
|
C | T | 10 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+4574C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223111 | ||||||
chr2:44223296
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 270 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.1134+4759T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223296 | ||||||
chr2:44223385
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.1134+4848G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223385 | ||||||
chr2:44223456
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0147 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1134+4919T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223456 | ||||||
chr2:44223692
|
T | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(69): Show | 74 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1134+5155T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223692 | ||||||
chr2:44223752
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1134+5215C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223752 | ||||||
chr2:44223814
|
T | TA | 30 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0037others(27): Show | 31 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1134+5307dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | |||||
chr2:44223814
|
TA | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(50): Show | 55 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1134+5307delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | |||||
chr2:44223814
|
TAA | T | 40 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0161others(37): Show | 40 | HG00544.hp1 HG00597.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1134+5306_1134+530 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | |||||
chr2:44223814
|
TAAA | T | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 119 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1134+5305_1134+530 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | |||||
chr2:44223814
|
TAAAA | T | 8 | a0001c0001t0001g0228a0001c0001t0001g0247a0001c0001t0001g0252others(5): Show | 8 | HG02897.hp2 HG03486.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.1134+5304_1134+530 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | |||||
chr2:44223814
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1134+5297_1134+530 others(15): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | |||||
chr2:44223815
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0004c0003t0001g0013 | 3 | HG02559.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1134+5278A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223815 | ||||||
chr2:44223831
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0278 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1134+5296_1134+531 others(22): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223831 | |||||
chr2:44223843
|
A | AG | 4 | a0001c0001t0001g0108a0001c0001t0001g0199a0001c0001t0001g0268others(1): Show | 4 | HG01975.hp2 NA18522.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+5306_1134+530 others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223843 | ||||||
chr2:44223843
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0105others(2): Show | 5 | HG00741.hp1 HG02683.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+5306A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223843 | ||||||
chr2:44223858
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1134+5321A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223858 | ||||||
chr2:44223881
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(60): Show | 65 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1134+5344A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223881 | ||||||
chr2:44223896
|
G | C | 5 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0269others(2): Show | 5 | HG00639.hp1 HG01934.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+5359G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223896 | ||||||
chr2:44223908
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0314others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+5371A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223908 | ||||||
chr2:44223969
|
T | G | 3 | a0001c0001t0001g0152a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1134+5432T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223969 | ||||||
chr2:44223975
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1134+5438A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223975 | ||||||
chr2:44224067
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1134+5530A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224067 | ||||||
chr2:44224128
|
T | A | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1134+5591T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224128 | ||||||
chr2:44224178
|
G | A | 4 | a0001c0001t0001g0170a0001c0001t0001g0344a0001c0001t0002g0033others(1): Show | 4 | HG00741.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134+5641G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224178 | ||||||
chr2:44224231
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1134+5694G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224231 | ||||||
chr2:44224323
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1134+5786C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224323 | ||||||
chr2:44224380
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 110 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1134+5843G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224380 | ||||||
chr2:44224455
|
C | CA | 12 | a0001c0001t0001g0027a0001c0001t0001g0194a0001c0001t0001g0271others(9): Show | 12 | HG02056.hp1 HG02074.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.1134+5938dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44224455 | |||||
chr2:44224455
|
CA | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(243): Show | 253 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.1134+5938delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44224455 | |||||
chr2:44224617
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1135-5796A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224617 | ||||||
chr2:44224694
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1135-5719A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224694 | ||||||
chr2:44224700
|
TAA | T | 151 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(148): Show | 154 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1135-5709_1135-570 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44224700 | |||||
chr2:44224710
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1135-5703G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224710 | ||||||
chr2:44224729
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1135-5684G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224729 | ||||||
chr2:44224988
|
C | T | 13 | a0001c0001t0001g0189a0001c0001t0001g0215a0001c0001t0001g0224others(10): Show | 13 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135-5425C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224988 | ||||||
chr2:44225015
|
T | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(57): Show | 62 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1135-5398T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225015 | ||||||
chr2:44225168
|
A | T | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-5245A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225168 | ||||||
chr2:44225205
|
T | C | 237 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 242 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1135-5208T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225205 | ||||||
chr2:44225215
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1135-5198G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225215 | ||||||
chr2:44225251
|
C | T | 150 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(147): Show | 153 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1135-5162C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225251 | ||||||
chr2:44225415
|
A | C | 6 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092others(3): Show | 6 | HG01074.hp2 HG01099.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-4998A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225415 | ||||||
chr2:44225541
|
C | G | 1 | a0001c0001t0002g0084 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1135-4872C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225541 | ||||||
chr2:44225598
|
G | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0052 | 2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1135-4815G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225598 | ||||||
chr2:44225679
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-4734C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225679 | ||||||
chr2:44225722
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1135-4691T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225722 | ||||||
chr2:44225777
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1135-4636C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225777 | ||||||
chr2:44225972
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0344 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-4441A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225972 | ||||||
chr2:44225976
|
C | CT | 6 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0260others(3): Show | 6 | HG01169.hp1 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-4420dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44225976 | |||||
chr2:44225976
|
CT | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 98 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1135-4420delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44225976 | |||||
chr2:44226062
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-4351G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226062 | ||||||
chr2:44226124
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1135-4289C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226124 | ||||||
chr2:44226135
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1135-4278C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226135 | ||||||
chr2:44226293
|
G | A | 5 | a0001c0001t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-4120G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226293 | ||||||
chr2:44226304
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135-4109T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226304 | ||||||
chr2:44226429
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1135-3984G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226429 | ||||||
chr2:44226444
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1135-3969C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226444 | ||||||
chr2:44226517
|
T | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0096others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135-3896T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226517 | ||||||
chr2:44226541
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1135-3872C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226541 | ||||||
chr2:44226683
|
A | G | 2 | a0001c0001t0002g0033a0001c0001t0002g0034 | 2 | HG00741.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1135-3730A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226683 | ||||||
chr2:44226735
|
CT | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(51): Show | 57 | HG00323.hp1 HG00642.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.1135-3654delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226735 | |||||
chr2:44226735
|
CTT | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 196 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1135-3655_1135-365 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226735 | |||||
chr2:44226735
|
CTTT | C | 8 | a0001c0001t0001g0119a0001c0001t0001g0207a0001c0001t0001g0229others(5): Show | 8 | HG01069.hp2 HG01981.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135-3656_1135-365 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226735 | |||||
chr2:44226778
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1135-3635G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226778 | ||||||
chr2:44226899
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1135-3514C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226899 | ||||||
chr2:44226908
|
C | G | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0220 | 3 | HG02486.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1135-3505C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226908 | ||||||
chr2:44226932
|
T | TTTTA | 117 | a0001c0001t0001g0017a0001c0001t0001g0132a0001c0001t0001g0154others(114): Show | 117 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1135-3443_1135-344 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | |||||
chr2:44226932
|
T | TTTTATTT others(1): Show |
47 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(44): Show | 48 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1135-3447_1135-344 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | |||||
chr2:44226932
|
T | TTTTATTT others(5): Show |
6 | a0001c0001t0001g0010a0001c0001t0001g0187a0001c0001t0001g0269others(3): Show | 6 | HG01934.hp2 HG02074.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-3451_1135-344 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | |||||
chr2:44226932
|
TTTTA | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0027others(26): Show | 30 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1135-3443_1135-344 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | |||||
chr2:44226932
|
TTTTATTT others(1): Show |
T | 7 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344others(4): Show | 7 | HG02055.hp2 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-3447_1135-344 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | |||||
chr2:44226932
|
TTTTATTT others(5): Show |
T | 6 | a0001c0001t0001g0011a0001c0001t0001g0023a0002c0002t0001g0024others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-3451_1135-344 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | |||||
chr2:44226932
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0309 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1135-3455_1135-344 others(20): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | |||||
chr2:44226967
|
TATTTATG others(5): Show |
T | 1 | a0001c0001t0001g0135 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1135-3443_1135-343 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226967 | |||||
chr2:44226970
|
T | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-3443T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226970 | ||||||
chr2:44226971
|
T | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0344 | 3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-3442T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226971 | ||||||
chr2:44226971
|
TATGA | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0104others(26): Show | 31 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1135-3421_1135-341 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226971 | |||||
chr2:44226971
|
TATGAATG others(1): Show |
T | 3 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0001g0149 | 3 | HG02735.hp1 HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1135-3425_1135-341 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226971 | |||||
chr2:44226974
|
G | T | 29 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0001g0113others(26): Show | 29 | HG00438.hp2 HG00621.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.1135-3439G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226974 | ||||||
chr2:44226975
|
A | T | 29 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0001g0113others(26): Show | 29 | HG00438.hp2 HG00621.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.1135-3438A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226975 | ||||||
chr2:44226978
|
G | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(53): Show | 58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1135-3435G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226978 | ||||||
chr2:44226979
|
A | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(53): Show | 58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1135-3434A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226979 | ||||||
chr2:44227301
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1135-3112T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227301 | ||||||
chr2:44227454
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1135-2959G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227454 | ||||||
chr2:44227464
|
A | G | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135-2949A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227464 | ||||||
chr2:44227482
|
A | T | 3 | a0001c0001t0001g0185a0001c0001t0001g0268a0001c0001t0001g0304 | 3 | NA18944.hp1 NA18986.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1135-2931A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227482 | ||||||
chr2:44227495
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-2918G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227495 | ||||||
chr2:44227503
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1135-2910C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227503 | ||||||
chr2:44227518
|
C | CT | 17 | a0001c0001t0001g0017a0001c0001t0001g0125a0001c0001t0001g0170others(14): Show | 17 | HG00544.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1135-2879dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227518 | |||||
chr2:44227518
|
C | CTT | 64 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0027others(61): Show | 66 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1135-2880_1135-287 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227518 | |||||
chr2:44227643
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1135-2770C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227643 | ||||||
chr2:44227740
|
G | A | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 77 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1135-2673G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227740 | ||||||
chr2:44227785
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1135-2628G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227785 | ||||||
chr2:44227879
|
G | A | 1 | a0001c0001t0002g0186 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1135-2534G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227879 | ||||||
chr2:44227912
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0256 | 2 | HG00597.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1135-2501T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227912 | ||||||
chr2:44227922
|
C | CT | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(69): Show | 75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1135-2474dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227922 | |||||
chr2:44227922
|
CT | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.1135-2474delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227922 | |||||
chr2:44228007
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0168others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-2406C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228007 | ||||||
chr2:44228073
|
C | T | 2 | a0001c0001t0003g0346a0001c0001t0003g0348 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1135-2340C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228073 | ||||||
chr2:44228080
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135-2333G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228080 | ||||||
chr2:44228158
|
G | A | 1 | a0001c0001t0008g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-2255G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228158 | ||||||
chr2:44228187
|
C | CT | 282 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 289 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1135-2206dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228187 | |||||
chr2:44228187
|
C | CTT | 10 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0118others(7): Show | 10 | HG00438.hp2 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-2207_1135-220 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228187 | |||||
chr2:44228187
|
CT | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0154others(7): Show | 12 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1135-2206delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228187 | |||||
chr2:44228227
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-2186G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228227 | ||||||
chr2:44228249
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1135-2164A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228249 | ||||||
chr2:44228255
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1135-2158A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228255 | ||||||
chr2:44228269
|
CCTCAACC others(12): Show |
C | 4 | a0001c0001t0001g0215a0001c0001t0001g0235a0001c0001t0001g0238others(1): Show | 4 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2134_1135-211 others(23): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228269 | |||||
chr2:44228331
|
G | T | 4 | a0001c0001t0001g0215a0001c0001t0001g0235a0001c0001t0001g0238others(1): Show | 4 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2082G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228331 | ||||||
chr2:44228348
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0235a0001c0001t0001g0238others(1): Show | 4 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2065A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228348 | ||||||
chr2:44228513
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-1900A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228513 | ||||||
chr2:44228572
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1135-1841A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228572 | ||||||
chr2:44228593
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1135-1820T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228593 | ||||||
chr2:44228622
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1135-1791A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228622 | ||||||
chr2:44228724
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0150a0001c0001t0001g0152others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135-1689A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228724 | ||||||
chr2:44228811
|
TTGAC | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0214a0001c0001t0001g0314others(1): Show | 4 | HG02886.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-1598_1135-159 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228811 | |||||
chr2:44228971
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135-1442T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228971 | ||||||
chr2:44229109
|
G | A | 5 | a0001c0001t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-1304G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229109 | ||||||
chr2:44229190
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1135-1223A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229190 | ||||||
chr2:44229272
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-1141A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229272 | ||||||
chr2:44229304
|
A | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(36): Show | 41 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.1135-1109A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229304 | ||||||
chr2:44229397
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1135-1016C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229397 | ||||||
chr2:44229408
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1135-1005A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229408 | ||||||
chr2:44229515
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135-898A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229515 | ||||||
chr2:44229610
|
A | T | 1 | a0001c0001t0001g0337 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1135-803A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229610 | ||||||
chr2:44229700
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1135-713T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229700 | ||||||
chr2:44229708
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0016others(21): Show | 26 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1135-705G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229708 | ||||||
chr2:44230095
|
G | GT | 4 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-315dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44230095 | |||||
chr2:44230192
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0314 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1135-221C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44230192 |