Item | Value |
---|---|
geneid | 5096 |
ensemblid | ENSG00000114054.14 |
hgncid | 8654 |
symbol | PCCB |
name | propionyl-CoA carboxylase subunit beta |
refseq_nuc | NM_000532.5 |
refseq_prot | NP_000523.2 |
ensembl_nuc | ENST00000251654.9 |
ensembl_prot | ENSP00000251654.4 |
mane_status | MANE Select |
chr | chr3 |
start | 136250340 |
end | 136330169 |
strand | + |
ver | v1.2 |
region | chr3:136250340-136330169 |
region5000 | chr3:136245340-136335169 |
regionname0 | PCCB_chr3_136250340_136330169 |
regionname5000 | PCCB_chr3_136245340_136335169 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 539 | 293 | 85 | 57 | 105 | 10 | 34 | 79 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0002 | 0/0 | 539 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0003 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0004 | 0/0 | 539 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0005 | 0/0 | 539 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0006 | 0/0 | 539 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0007 | 0/0 | 539 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1620 | 290 | 84 | 56 | 105 | 9 | 34 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0002 | 0/0 | 1620 | 2 | 1 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0003 | 0/0 | 1620 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0004 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0005 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0006 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0007 | 0/0 | 1620 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0008 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
c0009 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 180 | 297 | 85 | 58 | 106 | 10 | 36 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
t0002 | 0/0 | 180 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
t0003 | 0/0 | 180 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1620 | 290 | 84 | 56 | 105 | 9 | 34 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0001c0002 | 0/0 | 1620 | 2 | 1 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0001c0009 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0002c0003 | 0/0 | 1620 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0003c0004 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0004c0005 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0005c0008 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0006c0007 | 0/0 | 1620 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0007c0006 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1799 | 287 | 81 | 56 | 105 | 9 | 34 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0001c0001t0002 | 0/0 | 1799 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0001c0001t0003 | 0/0 | 1799 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0001c0002t0001 | 0/0 | 1799 | 2 | 1 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0001c0009t0001 | 0/0 | 1799 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0002c0003t0001 | 0/0 | 1799 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0003c0004t0001 | 0/0 | 1817 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0004c0005t0001 | 0/0 | 1799 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0005c0008t0001 | 0/0 | 1799 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0006c0007t0001 | 0/0 | 1799 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
a0007c0006t0001 | 0/0 | 1799 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | copy fasta | chr3 | 136245340 | 136335169 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0001c0009t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0002c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0003c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0004c0005t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0005c0008t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0006c0007t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
a0007c0006t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0009 | t0001 | g0110 | EUR | GBR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01358 | hp1 | a0006 | c0007 | t0001 | g0222 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03041 | hp2 | a0002 | c0003 | t0001 | g0208 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03209 | hp2 | a0004 | c0005 | t0001 | g0286 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03491 | hp2 | a0005 | c0008 | t0001 | g0230 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03831 | hp2 | a0007 | c0006 | t0001 | g0114 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19057 | hp1 | a0003 | c0004 | t0001 | g0083 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | YRI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ASW | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ASW | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | GIH | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | GIH | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0194 | REF | REF | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0219 | REF | REF | PCCB_chr3_136245340_136335169 | PCCB | chr3 | 136245340 | 136335169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:136250376
|
A | ATGGCGGC others(11): Show |
1 | a0003 | 1 | NA19057.hp1 | disruptive_inframe_insertion | MODERATE | c.11_28dupCATTACGGGT others(8): Show |
p.Ala4_Ala9dup | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/15 | 65/1799 | 29/1620 | 10/539 | INFO_REALIGN_3_PRIME | chr3 | 136250376 | |
chr3:136256589
|
G | A | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.338G>A | p.Arg113Gln | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/15 | 374/1799 | 338/1620 | 113/539 | chr3 | 136256589 | ||
chr3:136297962
|
C | G | 1 | a0002 | 2 | HG02886.hp2 HG03041.hp2 |
missense_variant | MODERATE | c.774C>G | p.His258Gln | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/15 | 810/1799 | 774/1620 | 258/539 | chr3 | 136297962 | ||
chr3:136327686
|
C | T | 1 | a0005 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1352C>T | p.Thr451Ile | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/15 | 1388/1799 | 1352/1620 | 451/539 | chr3 | 136327686 | ||
chr3:136327706
|
G | A | 1 | a0007 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.1372G>A | p.Ala458Thr | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/15 | 1408/1799 | 1372/1620 | 458/539 | chr3 | 136327706 | ||
chr3:136328849
|
C | T | 1 | a0006 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1490C>T | p.Ala497Val | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/15 | 1526/1799 | 1490/1620 | 497/539 | chr3 | 136328849 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:136283839
|
G | A | 1 | a0001c0002 | 2 | HG00735.hp1 NA19240.hp2 |
splice_region_variant&synonymous_variant | LOW | c.546G>A | p.Arg182Arg | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/15 | 582/1799 | 546/1620 | 182/539 | chr3 | 136283839 | ||
chr3:136283905
|
C | T | 1 | a0001c0009 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.612C>T | p.Ala204Ala | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/15 | 648/1799 | 612/1620 | 204/539 | chr3 | 136283905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:136330070
|
C | T | 1 | a0001c0001t0003 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 15/15 | 44 | chr3 | 136330070 | |||||
chr3:136330117
|
C | A | 1 | a0001c0001t0002 | 2 | HG03139.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*91C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 15/15 | 91 | chr3 | 136330117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:136250613
|
T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+55T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250613 | ||||||
chr3:136250663
|
C | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.183+105C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250663 | ||||||
chr3:136250695
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+137G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250695 | ||||||
chr3:136250705
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.183+147A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250705 | ||||||
chr3:136250759
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+201T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250759 | ||||||
chr3:136250821
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+263A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250821 | ||||||
chr3:136250913
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.183+355T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136250913 | ||||||
chr3:136251087
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.183+529G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251087 | ||||||
chr3:136251116
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.183+558C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251116 | ||||||
chr3:136251335
|
A | G | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+777A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251335 | ||||||
chr3:136251356
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+798G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251356 | ||||||
chr3:136251438
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.183+880C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251438 | ||||||
chr3:136251646
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+1088A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251646 | ||||||
chr3:136251862
|
C | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(16): Show | 19 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.183+1304C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136251862 | ||||||
chr3:136252438
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG00544.hp1 HG00609.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+1880A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252438 | ||||||
chr3:136252526
|
A | AT | 6 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG00597.hp2 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+1983dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252526 | |||||
chr3:136252526
|
AT | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+1983delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252526 | |||||
chr3:136252662
|
A | AT | 36 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0034others(33): Show | 37 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+2125dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252662 | |||||
chr3:136252695
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+2137G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252695 | ||||||
chr3:136252695
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.183+2137G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252695 | ||||||
chr3:136252851
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.183+2293C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252851 | ||||||
chr3:136252907
|
TG | T | 20 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(17): Show | 20 | HG00280.hp2 HG00733.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.183+2350delG | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252907 | ||||||
chr3:136252908
|
G | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG00741.hp2 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+2350G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252908 | ||||||
chr3:136252908
|
GT | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 177 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.183+2363delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136252908 | |||||
chr3:136252961
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+2403A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136252961 | ||||||
chr3:136253008
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.183+2450C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253008 | ||||||
chr3:136253015
|
G | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2457G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253015 | ||||||
chr3:136253082
|
G | GT | 37 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(34): Show | 39 | HG00597.hp2 HG00642.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.183+2549dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | |||||
chr3:136253082
|
G | GTT | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(106): Show | 111 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.183+2548_183+2549d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | |||||
chr3:136253082
|
G | GTTT | 25 | a0001c0001t0001g0015a0001c0001t0001g0121a0001c0001t0001g0122others(22): Show | 25 | HG00423.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.183+2547_183+2549d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | |||||
chr3:136253082
|
GTTTTT | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2545_183+2549d others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253082 | |||||
chr3:136253086
|
T | TTTG | 7 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG01433.hp1 HG02300.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2530_183+2531i others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253086 | |||||
chr3:136253087
|
T | TTG | 21 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(18): Show | 21 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.183+2530_183+2531i others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253087 | |||||
chr3:136253088
|
T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2530T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253088 | ||||||
chr3:136253150
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.183+2592C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253150 | ||||||
chr3:136253279
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.184-2577C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253279 | ||||||
chr3:136253325
|
G | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.184-2531G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253325 | ||||||
chr3:136253439
|
C | T | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-2417C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253439 | ||||||
chr3:136253566
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.184-2290G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253566 | ||||||
chr3:136253585
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.184-2271A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253585 | ||||||
chr3:136253664
|
A | AT | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0034others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-2171dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253664 | |||||
chr3:136253664
|
AT | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(6): Show | 9 | HG00099.hp2 HG00544.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-2171delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136253664 | |||||
chr3:136253755
|
C | T | 42 | a0001c0001t0001g0202a0001c0001t0001g0223a0001c0001t0001g0224others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.184-2101C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253755 | ||||||
chr3:136253952
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.184-1904T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136253952 | ||||||
chr3:136254012
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.184-1844A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254012 | ||||||
chr3:136254080
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.184-1776T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254080 | ||||||
chr3:136254208
|
C | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-1648C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254208 | ||||||
chr3:136254309
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1547C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254309 | ||||||
chr3:136254326
|
C | T | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-1530C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254326 | ||||||
chr3:136254366
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1490G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254366 | ||||||
chr3:136254462
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-1394C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254462 | ||||||
chr3:136254515
|
T | G | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.184-1341T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254515 | ||||||
chr3:136254518
|
C | CT | 30 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(27): Show | 30 | HG00733.hp1 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.184-1308dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
C | CTT | 21 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0048others(18): Show | 22 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.184-1309_184-1308d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
C | CTTT | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(56): Show | 61 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.184-1310_184-1308d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
C | CTTTT | 38 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0042others(35): Show | 38 | HG00621.hp2 HG00735.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.184-1311_184-1308d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
C | CTTTTT | 11 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG00099.hp1 HG01928.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-1312_184-1308d others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
CT | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0138a0001c0001t0001g0142others(46): Show | 50 | HG00280.hp1 HG00280.hp2 HG01361.hp1 others(47): Show |
intron_variant | MODIFIER | c.184-1308delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
CTT | C | 9 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0224others(6): Show | 9 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-1309_184-1308d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.184-1317_184-1308d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0184 | 3 | HG02109.hp1 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.184-1318_184-1308d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.184-1321_184-1308d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254518
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0002t0001g0030a0001c0002t0001g0032 | 2 | HG00735.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.184-1322_184-1308d others(17): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254518 | |||||
chr3:136254536
|
TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1319_184-1307d others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254536 | ||||||
chr3:136254549
|
A | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0293a0001c0001t0002g0044others(1): Show | 4 | HG03139.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1307A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254549 | ||||||
chr3:136254668
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.184-1188G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254668 | ||||||
chr3:136254713
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.184-1143C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254713 | ||||||
chr3:136254786
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.184-1070C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254786 | ||||||
chr3:136254816
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0220 | 2 | HG01496.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.184-1040C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254816 | ||||||
chr3:136254830
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-1026C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254830 | ||||||
chr3:136254878
|
CTT | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-965_184-964del others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr3 | 136254878 | |||||
chr3:136254894
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.184-962G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254894 | ||||||
chr3:136254946
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.184-910G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136254946 | ||||||
chr3:136255027
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.184-829C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255027 | ||||||
chr3:136255076
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-780A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255076 | ||||||
chr3:136255212
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.184-644T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255212 | ||||||
chr3:136255309
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.184-547A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255309 | ||||||
chr3:136255322
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.184-534G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255322 | ||||||
chr3:136255374
|
G | A | 20 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(17): Show | 20 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-482G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255374 | ||||||
chr3:136255385
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.184-471G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255385 | ||||||
chr3:136255628
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.184-228A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255628 | ||||||
chr3:136255718
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.184-138G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255718 | ||||||
chr3:136255769
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-87C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255769 | ||||||
chr3:136255785
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-71A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 1/14 | chr3 | 136255785 | ||||||
chr3:136256408
|
T | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.304-147T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 2/14 | chr3 | 136256408 | ||||||
chr3:136256519
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304-36G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 2/14 | chr3 | 136256519 | ||||||
chr3:136256654
|
T | C | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0089others(11): Show | 14 | HG00621.hp2 HG02080.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.372+31T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136256654 | ||||||
chr3:136256908
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.372+285G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136256908 | ||||||
chr3:136256908
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.372+285G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136256908 | ||||||
chr3:136257240
|
G | T | 1 | a0001c0001t0001g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.372+617G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257240 | ||||||
chr3:136257285
|
A | C | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+662A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257285 | ||||||
chr3:136257521
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA18959.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.372+898C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257521 | ||||||
chr3:136257622
|
C | T | 8 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(5): Show | 8 | HG02165.hp2 HG02523.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+999C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257622 | ||||||
chr3:136257907
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.372+1284T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257907 | ||||||
chr3:136257982
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.372+1359G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136257982 | ||||||
chr3:136257991
|
A | ATGCATTT others(11): Show |
1 | a0001c0001t0001g0180 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.372+1370_372+1387d others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136257991 | |||||
chr3:136258075
|
A | ATTTC | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 62 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.372+1455_372+1456i others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136258075 | |||||
chr3:136258126
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0044others(2): Show | 5 | HG01496.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1503C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258126 | ||||||
chr3:136258137
|
GAGAT | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+1518_372+1521d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136258137 | |||||
chr3:136258167
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1544A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258167 | ||||||
chr3:136258198
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 188 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.372+1575G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258198 | ||||||
chr3:136258335
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+1712C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258335 | ||||||
chr3:136258463
|
A | G | 6 | a0001c0001t0001g0201a0001c0001t0001g0215a0001c0001t0001g0216others(3): Show | 6 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+1840A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258463 | ||||||
chr3:136258571
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.373-1908T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258571 | ||||||
chr3:136258599
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.373-1880G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136258599 | ||||||
chr3:136259187
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-1292C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259187 | ||||||
chr3:136259248
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.373-1231C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259248 | ||||||
chr3:136259250
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.373-1229T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259250 | ||||||
chr3:136259310
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.373-1169C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259310 | ||||||
chr3:136259357
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.373-1122C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259357 | ||||||
chr3:136259396
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.373-1083C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259396 | ||||||
chr3:136259397
|
G | A | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.373-1082G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259397 | ||||||
chr3:136259470
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG00544.hp1 HG01496.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.373-1009G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259470 | ||||||
chr3:136259601
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.373-878T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259601 | ||||||
chr3:136259783
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-696C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259783 | ||||||
chr3:136259813
|
A | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-666A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259813 | ||||||
chr3:136259955
|
T | C | 20 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(17): Show | 20 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.373-524T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136259955 | ||||||
chr3:136260031
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-448T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260031 | ||||||
chr3:136260057
|
T | TTTTTG | 5 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 6 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-391_373-387dup others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | |||||
chr3:136260057
|
TTTTTG | T | 14 | a0001c0001t0001g0200a0001c0001t0001g0204a0001c0001t0001g0206others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-391_373-387del others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | |||||
chr3:136260057
|
TTTTTGTT others(3): Show |
T | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.373-396_373-387del others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | |||||
chr3:136260057
|
TTTTTGTT others(8): Show |
T | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.373-401_373-387del others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 136260057 | |||||
chr3:136260223
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | NA18953.hp2 NA18964.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.373-256G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260223 | ||||||
chr3:136260306
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 7 | HG01243.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.373-173G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260306 | ||||||
chr3:136260355
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.373-124G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 3/14 | chr3 | 136260355 | ||||||
chr3:136260592
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.429+57T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260592 | ||||||
chr3:136260663
|
C | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429+128C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260663 | ||||||
chr3:136260842
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+307C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260842 | ||||||
chr3:136260844
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+309A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260844 | ||||||
chr3:136260856
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(110): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.429+321A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260856 | ||||||
chr3:136260921
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.429+386C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260921 | ||||||
chr3:136260936
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429+401A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136260936 | ||||||
chr3:136261027
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.429+492G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261027 | ||||||
chr3:136261089
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+554C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261089 | ||||||
chr3:136261137
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.429+602T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261137 | ||||||
chr3:136261139
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.429+604T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261139 | ||||||
chr3:136261221
|
T | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0176others(2): Show | 5 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+686T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261221 | ||||||
chr3:136261349
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-603C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261349 | ||||||
chr3:136261556
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.430-396A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261556 | ||||||
chr3:136261578
|
GA | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 72 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.430-371delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 136261578 | |||||
chr3:136261583
|
T | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 72 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.430-369T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261583 | ||||||
chr3:136261636
|
C | T | 5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG00609.hp1 HG01884.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-316C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261636 | ||||||
chr3:136261831
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(67): Show | 72 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.430-121C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261831 | ||||||
chr3:136261879
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.430-73T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 4/14 | chr3 | 136261879 | ||||||
chr3:136262112
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.543+47C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262112 | ||||||
chr3:136262177
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.543+112G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262177 | ||||||
chr3:136262312
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.543+247A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262312 | ||||||
chr3:136262470
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.543+405G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262470 | ||||||
chr3:136262785
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.543+720G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262785 | ||||||
chr3:136262856
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00544.hp1 HG01516.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+791C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262856 | ||||||
chr3:136262940
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+875T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136262940 | ||||||
chr3:136262954
|
G | GT | 18 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0041others(15): Show | 18 | HG00621.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+907dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136262954 | |||||
chr3:136262954
|
GT | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(98): Show | 103 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.543+907delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136262954 | |||||
chr3:136263079
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+1014C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263079 | ||||||
chr3:136263219
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+1154C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263219 | ||||||
chr3:136263254
|
G | GT | 41 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0047others(38): Show | 42 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.543+1206dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136263254 | |||||
chr3:136263254
|
G | GTT | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 202 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.543+1205_543+1206d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136263254 | |||||
chr3:136263254
|
G | GTTT | 47 | a0001c0001t0001g0026a0001c0001t0001g0099a0001c0001t0001g0108others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.543+1204_543+1206d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136263254 | |||||
chr3:136263346
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.543+1281A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263346 | ||||||
chr3:136263365
|
A | C | 1 | a0007c0006t0001g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.543+1300A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263365 | ||||||
chr3:136263478
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+1413C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263478 | ||||||
chr3:136263512
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.543+1447T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263512 | ||||||
chr3:136263575
|
A | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0202a0001c0001t0001g0203others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.543+1510A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263575 | ||||||
chr3:136263641
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543+1576G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263641 | ||||||
chr3:136263739
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+1674C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263739 | ||||||
chr3:136263740
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+1675G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263740 | ||||||
chr3:136263944
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0099 | 3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.543+1879A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263944 | ||||||
chr3:136263972
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.543+1907A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136263972 | ||||||
chr3:136264011
|
C | CA | 10 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0040others(7): Show | 10 | HG00423.hp2 HG01433.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.543+1962dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264011 | |||||
chr3:136264011
|
CA | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(48): Show | 52 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.543+1962delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264011 | |||||
chr3:136264247
|
A | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+2182A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264247 | ||||||
chr3:136264325
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0190 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.543+2260C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264325 | ||||||
chr3:136264396
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.543+2331G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264396 | ||||||
chr3:136264417
|
GTC | G | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.543+2357_543+2358d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264417 | |||||
chr3:136264430
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.543+2365A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264430 | ||||||
chr3:136264440
|
G | GTGTATAT others(7): Show |
5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(9): Show |
11 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0137others(8): Show | 11 | HG01123.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(11): Show |
6 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0169others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(13): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 6 | HG00738.hp1 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(15): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0175 | 3 | HG01109.hp1 HG01255.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(24): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(17): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0161a0001c0001t0001g0177 | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(19): Show |
1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(28): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(21): Show |
1 | a0001c0001t0001g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(30): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(23): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0167 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(32): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(25): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0198a0001c0001t0001g0294 | 3 | HG00741.hp2 HG03239.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(34): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(27): Show |
1 | a0001c0001t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(36): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(29): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 5 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(38): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(31): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0157 | 2 | HG01346.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(40): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(33): Show |
4 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0154others(1): Show | 4 | HG00280.hp2 HG00733.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2376_543+2377i others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(35): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0197 | 2 | HG01069.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.543+2376_543+2377i others(44): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATAT others(39): Show |
1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(48): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTATGT others(33): Show |
1 | a0001c0001t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTGTAT others(5): Show |
1 | a0001c0001t0001g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTGTAT others(9): Show |
1 | a0001c0001t0001g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTGTAT others(35): Show |
1 | a0001c0001t0001g0153 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(44): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTGTAT others(39): Show |
1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(48): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTGTAT others(45): Show |
1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.543+2376_543+2377i others(54): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264440
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+2376_543+2377i others(24): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264440 | |||||
chr3:136264442
|
A | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+2377A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264442 | ||||||
chr3:136264444
|
ATATG | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.543+2383_543+2386d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264444 | |||||
chr3:136264448
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0035others(61): Show | 65 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.543+2383G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264448 | ||||||
chr3:136264448
|
G | GTA | 6 | a0001c0001t0001g0013a0001c0001t0001g0204a0001c0001t0001g0260others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+2395_543+2396d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | |||||
chr3:136264448
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG00544.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.543+2384_543+2385i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | |||||
chr3:136264448
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0008 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.543+2384_543+2385i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | |||||
chr3:136264448
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.543+2384_543+2385i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | |||||
chr3:136264448
|
G | GTGTATAT others(13): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.543+2384_543+2385i others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264448 | |||||
chr3:136264458
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+2393A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264458 | ||||||
chr3:136264598
|
G | C | 12 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(9): Show | 12 | HG00733.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+2533G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264598 | ||||||
chr3:136264655
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0200others(25): Show | 29 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.543+2590C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264655 | ||||||
chr3:136264675
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0188 | 2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.543+2610C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264675 | ||||||
chr3:136264710
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.543+2645A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264710 | ||||||
chr3:136264874
|
C | CA | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(110): Show | 115 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.543+2830dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264874 | |||||
chr3:136264874
|
C | CAA | 28 | a0001c0001t0001g0037a0001c0001t0001g0064a0001c0001t0001g0074others(25): Show | 28 | HG00280.hp2 HG00597.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.543+2829_543+2830d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264874 | |||||
chr3:136264874
|
CA | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.543+2830delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136264874 | |||||
chr3:136264917
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+2852C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264917 | ||||||
chr3:136264924
|
G | A | 8 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0173others(5): Show | 8 | HG00738.hp1 HG01109.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+2859G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264924 | ||||||
chr3:136264955
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2890G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136264955 | ||||||
chr3:136265021
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2956C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265021 | ||||||
chr3:136265028
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.543+2963T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265028 | ||||||
chr3:136265219
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543+3154T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265219 | ||||||
chr3:136265221
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+3156T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265221 | ||||||
chr3:136265293
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0223others(2): Show | 5 | HG02080.hp1 NA18986.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+3228T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265293 | ||||||
chr3:136265300
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.543+3235A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265300 | ||||||
chr3:136265581
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543+3516A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265581 | ||||||
chr3:136265723
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.543+3658G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265723 | ||||||
chr3:136265767
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.543+3702A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265767 | ||||||
chr3:136265830
|
G | GT | 20 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(17): Show | 20 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+3778dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136265830 | |||||
chr3:136265830
|
GT | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+3778delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136265830 | |||||
chr3:136265927
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+3862G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136265927 | ||||||
chr3:136266124
|
A | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+4059A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266124 | ||||||
chr3:136266131
|
G | GT | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(3): Show | 6 | HG01175.hp2 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+4081dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136266131 | |||||
chr3:136266133
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+4068T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266133 | ||||||
chr3:136266415
|
C | CACCGCAC others(151): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+4472_543+4473i others(160): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136266415 | |||||
chr3:136266584
|
G | C | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543+4519G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266584 | ||||||
chr3:136266982
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.543+4917A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136266982 | ||||||
chr3:136267083
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+5018C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267083 | ||||||
chr3:136267245
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 203 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.543+5180A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267245 | ||||||
chr3:136267596
|
T | G | 29 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(26): Show | 29 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+5531T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267596 | ||||||
chr3:136267702
|
T | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+5637T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267702 | ||||||
chr3:136267718
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+5653C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136267718 | ||||||
chr3:136267944
|
C | CT | 25 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(22): Show | 25 | HG00609.hp1 HG01255.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.543+5898dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136267944 | |||||
chr3:136267944
|
C | CTT | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+5897_543+5898d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136267944 | |||||
chr3:136267944
|
CT | C | 12 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0064others(9): Show | 12 | HG00323.hp2 HG00733.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+5898delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136267944 | |||||
chr3:136268065
|
C | CGT | 106 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(103): Show | 107 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.543+6019_543+6020d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268065 | |||||
chr3:136268065
|
C | CGTGT | 6 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0038others(3): Show | 7 | HG02630.hp2 HG03041.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+6017_543+6020d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268065 | |||||
chr3:136268084
|
G | GTGTGTAG others(3): Show |
3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.543+6020_543+6021i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268084 | |||||
chr3:136268084
|
G | GTGTGTAG others(11): Show |
1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.543+6020_543+6021i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268084 | |||||
chr3:136268085
|
T | TGTGTAGA others(5): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.543+6020_543+6021i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268085 | ||||||
chr3:136268085
|
TAG | T | 23 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0138others(20): Show | 23 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+6022_543+6023d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268085 | |||||
chr3:136268086
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0176 | 2 | HG01346.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.543+6021A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268086 | ||||||
chr3:136268087
|
G | GAGATATA others(5): Show |
1 | a0001c0001t0001g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.543+6023_543+6024i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATAT | 8 | a0001c0001t0001g0181a0001c0001t0001g0187a0001c0001t0001g0206others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+6053_543+6056d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATAGA others(3): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | HG02895.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.543+6027_543+6028i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATAGA others(5): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029 | 3 | HG03486.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.543+6027_543+6028i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATAGA others(7): Show |
1 | a0001c0002t0001g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.543+6027_543+6028i others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATAGA others(9): Show |
1 | a0001c0002t0001g0032 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.543+6027_543+6028i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATAGA others(11): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0024 | 2 | HG01243.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.543+6027_543+6028i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATAT | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0120others(10): Show | 15 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+6051_543+6056d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(1): Show |
9 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0205others(6): Show | 9 | HG02109.hp2 HG02572.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+6049_543+6056d others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(3): Show |
10 | a0001c0001t0001g0034a0001c0001t0001g0203a0001c0001t0001g0227others(7): Show | 10 | HG00323.hp1 HG00621.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+6047_543+6056d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(5): Show |
12 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0228others(9): Show | 12 | HG01243.hp2 HG02080.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+6045_543+6056d others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(7): Show |
4 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0246others(1): Show | 4 | HG00280.hp1 NA18952.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+6043_543+6056d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(9): Show |
4 | a0001c0001t0001g0214a0001c0001t0001g0234a0001c0001t0001g0245others(1): Show | 4 | HG00597.hp2 HG01358.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+6041_543+6056d others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(11): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0279 | 2 | NA18989.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.543+6039_543+6056d others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(15): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | NA18963.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.543+6035_543+6056d others(24): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | GATATATA others(5): Show |
1 | a0001c0001t0001g0241 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.543+6030_543+6031i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
G | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG01346.hp2 HG01891.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+6022G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268087 | ||||||
chr3:136268087
|
GAT | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(63): Show | 69 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.543+6055_543+6056d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
GATATAT | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0157a0001c0001t0001g0161others(8): Show | 12 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+6051_543+6056d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
GATATATA others(1): Show |
G | 5 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 5 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+6049_543+6056d others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
GATATATA others(3): Show |
G | 3 | a0001c0001t0001g0168a0001c0001t0001g0179a0001c0001t0001g0220 | 3 | HG01123.hp2 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.543+6047_543+6056d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
GATATATA others(7): Show |
G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.543+6043_543+6056d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
GATATATA others(9): Show |
G | 1 | a0001c0001t0001g0010 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.543+6041_543+6056d others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
GATATATA others(11): Show |
G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG02135.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+6039_543+6056d others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268087
|
GATATATA others(29): Show |
G | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.543+6041_543+6076d others(38): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268087 | |||||
chr3:136268088
|
A | G | 25 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0138others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+6023A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268088 | ||||||
chr3:136268090
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.543+6042_543+6043i others(20): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268090 | |||||
chr3:136268090
|
A | G | 25 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0138others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+6025A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268090 | ||||||
chr3:136268091
|
T | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0176 | 2 | HG01433.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.543+6026T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268091 | ||||||
chr3:136268092
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.543+6027A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268092 | ||||||
chr3:136268093
|
T | G | 25 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0138others(22): Show | 25 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.543+6028T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268093 | ||||||
chr3:136268094
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0031 | 3 | HG01433.hp2 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.543+6044_543+6045i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268094 | |||||
chr3:136268094
|
A | ATATATAT others(7): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG00738.hp2 HG01106.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+6042_543+6043i others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268094 | |||||
chr3:136268094
|
A | ATATATG | 13 | a0001c0001t0001g0055a0001c0001t0001g0089a0001c0001t0001g0090others(10): Show | 13 | HG00621.hp2 HG01255.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.543+6034_543+6035i others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268094 | |||||
chr3:136268095
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.543+6030T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268095 | ||||||
chr3:136268095
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0242a0001c0001t0001g0257 | 2 | HG00423.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.543+6041_543+6042i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268095 | |||||
chr3:136268096
|
A | ATATG | 19 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0067others(16): Show | 19 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.543+6034_543+6035i others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268096 | |||||
chr3:136268096
|
A | ATATGTAT others(23): Show |
1 | a0001c0001t0001g0064 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.543+6034_543+6035i others(32): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268096 | |||||
chr3:136268097
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.543+6032T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268097 | ||||||
chr3:136268098
|
A | ATG | 3 | a0001c0001t0001g0043a0001c0001t0001g0065a0001c0001t0001g0158 | 3 | HG01928.hp1 HG02132.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.543+6034_543+6035i others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | |||||
chr3:136268098
|
A | ATGTATAT others(21): Show |
1 | a0001c0001t0001g0069 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.543+6034_543+6035i others(30): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | |||||
chr3:136268098
|
A | ATGTATAT others(41): Show |
1 | a0001c0001t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543+6034_543+6035i others(50): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | |||||
chr3:136268098
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+6053_543+6076d others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268098 | |||||
chr3:136268099
|
T | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0138others(21): Show | 24 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.543+6034T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268099 | ||||||
chr3:136268100
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0068others(3): Show | 6 | HG00609.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+6035A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268100 | ||||||
chr3:136268101
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.543+6036T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268101 | ||||||
chr3:136268102
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(61): Show | 66 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.543+6037A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268102 | ||||||
chr3:136268105
|
T | TAC | 14 | a0001c0001t0001g0047a0001c0001t0001g0201a0001c0001t0001g0212others(11): Show | 14 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+6041_543+6042i others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268105 | |||||
chr3:136268107
|
T | C | 7 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+6042T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268107 | ||||||
chr3:136268107
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.543+6042T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268107 | ||||||
chr3:136268116
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.543+6051A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268116 | ||||||
chr3:136268120
|
A | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0068others(2): Show | 5 | HG00609.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+6055A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268120 | ||||||
chr3:136268122
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 10 | HG00609.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+6057G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268122 | ||||||
chr3:136268122
|
G | GTA | 3 | a0001c0001t0001g0047a0001c0001t0001g0064a0001c0001t0001g0094 | 3 | HG00621.hp2 HG02523.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.543+6075_543+6076d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268122 | |||||
chr3:136268124
|
A | G | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0176others(5): Show | 8 | HG01496.hp1 HG01496.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+6059A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268124 | ||||||
chr3:136268136
|
A | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 84 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.543+6071A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268136 | ||||||
chr3:136268314
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0273a0001c0001t0001g0281others(1): Show | 5 | HG00642.hp2 HG01175.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+6249G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268314 | ||||||
chr3:136268465
|
G | GT | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(100): Show | 105 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.543+6417dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268465 | |||||
chr3:136268465
|
G | GTT | 11 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0085others(8): Show | 11 | HG00323.hp2 HG01928.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+6416_543+6417d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136268465 | |||||
chr3:136268543
|
A | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.543+6478A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268543 | ||||||
chr3:136268564
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.543+6499A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268564 | ||||||
chr3:136268890
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.543+6825G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268890 | ||||||
chr3:136268899
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.543+6834T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268899 | ||||||
chr3:136268964
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.543+6899C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136268964 | ||||||
chr3:136269113
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7048T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269113 | ||||||
chr3:136269234
|
G | C | 1 | a0001c0002t0001g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.543+7169G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269234 | ||||||
chr3:136269344
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.543+7279G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269344 | ||||||
chr3:136269464
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7399C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269464 | ||||||
chr3:136269570
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.543+7505G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269570 | ||||||
chr3:136269607
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7542C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269607 | ||||||
chr3:136269663
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+7598A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269663 | ||||||
chr3:136269701
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0180 | 2 | NA18953.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.543+7636C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269701 | ||||||
chr3:136269742
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+7677C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269742 | ||||||
chr3:136269802
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.543+7737C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269802 | ||||||
chr3:136269810
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543+7745C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269810 | ||||||
chr3:136269815
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+7750G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269815 | ||||||
chr3:136269817
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.543+7752C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269817 | ||||||
chr3:136269822
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0084 | 2 | HG00597.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.543+7757C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269822 | ||||||
chr3:136269885
|
C | CA | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 23 | HG00544.hp1 HG00733.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+7842dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269885 | |||||
chr3:136269885
|
CA | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0035others(4): Show | 7 | HG01256.hp2 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+7842delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269885 | |||||
chr3:136269908
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.543+7843T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269908 | ||||||
chr3:136269933
|
C | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+7868C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269933 | ||||||
chr3:136269993
|
G | GT | 24 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 25 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.543+7944dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269993 | |||||
chr3:136269993
|
GT | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.543+7944delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136269993 | |||||
chr3:136269996
|
T | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+7931T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136269996 | ||||||
chr3:136270052
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543+7987A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270052 | ||||||
chr3:136270450
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 198 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.543+8385C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270450 | ||||||
chr3:136270505
|
A | T | 1 | a0001c0001t0001g0003 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.543+8440A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270505 | ||||||
chr3:136270505
|
AT | A | 20 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 20 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+8451delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136270505 | |||||
chr3:136270516
|
T | TC | 3 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0155 | 3 | HG00280.hp2 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.543+8454dupC | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136270516 | |||||
chr3:136270534
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(78): Show | 82 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.543+8469C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270534 | ||||||
chr3:136270566
|
C | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0274 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.543+8501C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270566 | ||||||
chr3:136270695
|
A | G | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+8630A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270695 | ||||||
chr3:136270697
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+8632G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270697 | ||||||
chr3:136270713
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0287 | 2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.543+8648T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270713 | ||||||
chr3:136270757
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.543+8692T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270757 | ||||||
chr3:136270829
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.543+8764C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270829 | ||||||
chr3:136270853
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0232 | 3 | HG02080.hp1 NA18986.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.543+8788A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270853 | ||||||
chr3:136270863
|
G | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 47 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.543+8798G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136270863 | ||||||
chr3:136271386
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.543+9321A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271386 | ||||||
chr3:136271398
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.543+9333A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271398 | ||||||
chr3:136271558
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+9493T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271558 | ||||||
chr3:136271689
|
T | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+9624T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271689 | ||||||
chr3:136271811
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+9746A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271811 | ||||||
chr3:136271972
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.543+9907A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136271972 | ||||||
chr3:136272036
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543+9971C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272036 | ||||||
chr3:136272039
|
A | T | 29 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(26): Show | 29 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+9974A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272039 | ||||||
chr3:136272046
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+9981G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272046 | ||||||
chr3:136272301
|
A | G | 28 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(25): Show | 29 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+10236A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272301 | ||||||
chr3:136272431
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.543+10366T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272431 | ||||||
chr3:136272600
|
T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+10535T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272600 | ||||||
chr3:136272732
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+10667A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272732 | ||||||
chr3:136272905
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.543+10840C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272905 | ||||||
chr3:136272927
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.543+10862C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272927 | ||||||
chr3:136272966
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-10871T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136272966 | ||||||
chr3:136273160
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.544-10677C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273160 | ||||||
chr3:136273417
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.544-10420C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273417 | ||||||
chr3:136273547
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.544-10290C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273547 | ||||||
chr3:136273578
|
CTTTTTTT others(19): Show |
C | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-10247_544-1022 others(30): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273578 | |||||
chr3:136273589
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-10248T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273589 | ||||||
chr3:136273590
|
CTTTTTTC others(3): Show |
C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-10240_544-1023 others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273590 | |||||
chr3:136273597
|
C | CT | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 55 | HG00597.hp2 HG00738.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.544-10218dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273597 | |||||
chr3:136273597
|
C | CTT | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0058others(6): Show | 9 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-10219_544-1021 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273597 | |||||
chr3:136273597
|
CT | C | 34 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(31): Show | 34 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.544-10218delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273597 | |||||
chr3:136273601
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.544-10236T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273601 | ||||||
chr3:136273603
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02055.hp1 HG02074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-10234T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273603 | ||||||
chr3:136273684
|
G | A | 1 | a0001c0001t0001g0001 | 2 | NA18945.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.544-10153G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273684 | ||||||
chr3:136273688
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.544-10149G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273688 | ||||||
chr3:136273747
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.544-10090C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273747 | ||||||
chr3:136273772
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-10065C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273772 | ||||||
chr3:136273781
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.544-10056G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273781 | ||||||
chr3:136273803
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.544-10034T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273803 | ||||||
chr3:136273911
|
C | CA | 13 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0221others(10): Show | 13 | HG01167.hp1 HG01516.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-9901dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273911 | |||||
chr3:136273911
|
CA | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(111): Show | 116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.544-9901delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273911 | |||||
chr3:136273911
|
CAA | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 60 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.544-9902_544-9901d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136273911 | |||||
chr3:136273994
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.544-9843C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136273994 | ||||||
chr3:136274058
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-9779T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274058 | ||||||
chr3:136274093
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.544-9744C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274093 | ||||||
chr3:136274228
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.544-9609G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274228 | ||||||
chr3:136274233
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-9604T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274233 | ||||||
chr3:136274264
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0107 | 2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.544-9573T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274264 | ||||||
chr3:136274334
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0107 | 2 | HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.544-9503G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274334 | ||||||
chr3:136274434
|
G | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0078others(2): Show | 5 | HG00323.hp2 HG01346.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-9403G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274434 | ||||||
chr3:136274592
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.544-9245A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274592 | ||||||
chr3:136274757
|
A | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.544-9080A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274757 | ||||||
chr3:136274809
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-9028G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274809 | ||||||
chr3:136274941
|
T | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-8896T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274941 | ||||||
chr3:136274978
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.544-8859T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136274978 | ||||||
chr3:136274985
|
G | GT | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0111others(1): Show | 4 | HG01928.hp2 NA18952.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-8844dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 136274985 | |||||
chr3:136275064
|
G | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.544-8773G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275064 | ||||||
chr3:136275201
|
G | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 197 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.544-8636G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275201 | ||||||
chr3:136275237
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-8600A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275237 | ||||||
chr3:136275269
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-8568G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275269 | ||||||
chr3:136275269
|
G | T | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.544-8568G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275269 | ||||||
chr3:136275626
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0272 | 2 | HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.544-8211C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275626 | ||||||
chr3:136275632
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.544-8205G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275632 | ||||||
chr3:136275796
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.544-8041C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275796 | ||||||
chr3:136275797
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 8 | HG00642.hp2 HG01175.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-8040G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275797 | ||||||
chr3:136275821
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-8016A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275821 | ||||||
chr3:136275863
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-7974C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275863 | ||||||
chr3:136275938
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.544-7899T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275938 | ||||||
chr3:136275946
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-7891T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275946 | ||||||
chr3:136275959
|
C | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 47 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.544-7878C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275959 | ||||||
chr3:136275969
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0287 | 2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.544-7868G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136275969 | ||||||
chr3:136276174
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.544-7663T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276174 | ||||||
chr3:136276185
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-7652T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276185 | ||||||
chr3:136276199
|
C | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG01943.hp2 HG02300.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-7638C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276199 | ||||||
chr3:136276405
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.544-7432A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276405 | ||||||
chr3:136276424
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0278 | 2 | HG01516.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.544-7413T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276424 | ||||||
chr3:136276523
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-7314C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276523 | ||||||
chr3:136276558
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.544-7279C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276558 | ||||||
chr3:136276605
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-7232C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276605 | ||||||
chr3:136276650
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-7187A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276650 | ||||||
chr3:136276656
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.544-7181T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276656 | ||||||
chr3:136276764
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0104others(1): Show | 4 | NA18943.hp1 NA18965.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-7073C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276764 | ||||||
chr3:136276958
|
C | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-6879C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136276958 | ||||||
chr3:136277073
|
C | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-6764C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277073 | ||||||
chr3:136277119
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.544-6718G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277119 | ||||||
chr3:136277165
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.544-6672A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277165 | ||||||
chr3:136277260
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0155 | 3 | HG00280.hp2 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.544-6577A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277260 | ||||||
chr3:136277466
|
T | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.544-6371T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277466 | ||||||
chr3:136277487
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.544-6350T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277487 | ||||||
chr3:136277492
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0123 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.544-6345C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277492 | ||||||
chr3:136277555
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-6282G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277555 | ||||||
chr3:136277560
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0259 | 3 | HG02258.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.544-6277C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277560 | ||||||
chr3:136277793
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.544-6044C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136277793 | ||||||
chr3:136278028
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(104): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.544-5809T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278028 | ||||||
chr3:136278264
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-5573C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278264 | ||||||
chr3:136278384
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.544-5453C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278384 | ||||||
chr3:136278588
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.544-5249C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278588 | ||||||
chr3:136278669
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-5168G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278669 | ||||||
chr3:136278754
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-5083A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278754 | ||||||
chr3:136278844
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.544-4993C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278844 | ||||||
chr3:136278901
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-4936T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278901 | ||||||
chr3:136278917
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-4920T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136278917 | ||||||
chr3:136279047
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-4790A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279047 | ||||||
chr3:136279131
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.544-4706T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279131 | ||||||
chr3:136279136
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-4701A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279136 | ||||||
chr3:136279263
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.544-4574A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279263 | ||||||
chr3:136279275
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(3): Show | 7 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-4562A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279275 | ||||||
chr3:136279334
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0187 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.544-4503T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279334 | ||||||
chr3:136279348
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-4489T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279348 | ||||||
chr3:136279611
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 203 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.544-4226T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279611 | ||||||
chr3:136279675
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-4162A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279675 | ||||||
chr3:136279679
|
A | T | 38 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(35): Show | 38 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.544-4158A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279679 | ||||||
chr3:136279706
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.544-4131C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279706 | ||||||
chr3:136279736
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-4101C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279736 | ||||||
chr3:136279737
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.544-4100G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279737 | ||||||
chr3:136279768
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-4069C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279768 | ||||||
chr3:136279793
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.544-4044G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279793 | ||||||
chr3:136279817
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-4020A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279817 | ||||||
chr3:136279828
|
T | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.544-4009T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279828 | ||||||
chr3:136279867
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.544-3970C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279867 | ||||||
chr3:136279975
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.544-3862A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136279975 | ||||||
chr3:136280389
|
C | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.544-3448C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280389 | ||||||
chr3:136280588
|
C | T | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.544-3249C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280588 | ||||||
chr3:136280773
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.544-3064A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280773 | ||||||
chr3:136280814
|
G | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0137others(1): Show | 4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-3023G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280814 | ||||||
chr3:136280933
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.544-2904T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280933 | ||||||
chr3:136280944
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-2893G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136280944 | ||||||
chr3:136281022
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.544-2815A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281022 | ||||||
chr3:136281249
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.544-2588T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281249 | ||||||
chr3:136281252
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.544-2585G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281252 | ||||||
chr3:136281305
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-2532C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281305 | ||||||
chr3:136281485
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544-2352T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281485 | ||||||
chr3:136281500
|
G | C | 1 | a0001c0001t0001g0274 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-2337G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281500 | ||||||
chr3:136281507
|
A | G | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG01123.hp1 HG02698.hp2 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.544-2330A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281507 | ||||||
chr3:136281636
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-2201T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281636 | ||||||
chr3:136281763
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.544-2074C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281763 | ||||||
chr3:136281769
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-2068T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281769 | ||||||
chr3:136281774
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.544-2063G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281774 | ||||||
chr3:136281817
|
G | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-2020G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281817 | ||||||
chr3:136281901
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.544-1936A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281901 | ||||||
chr3:136281904
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.544-1933T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136281904 | ||||||
chr3:136282368
|
C | G | 1 | a0006c0007t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.544-1469C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282368 | ||||||
chr3:136282370
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02280.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.544-1467G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282370 | ||||||
chr3:136282424
|
T | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-1413T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282424 | ||||||
chr3:136282520
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02280.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.544-1317G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282520 | ||||||
chr3:136282844
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.544-993C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282844 | ||||||
chr3:136282866
|
C | T | 2 | a0001c0001t0001g0085a0003c0004t0001g0083 | 2 | NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.544-971C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282866 | ||||||
chr3:136282903
|
A | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0168a0001c0001t0001g0170 | 3 | HG01255.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.544-934A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282903 | ||||||
chr3:136282945
|
G | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.544-892G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136282945 | ||||||
chr3:136283026
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.544-811A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136283026 | ||||||
chr3:136283050
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-787G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136283050 | ||||||
chr3:136283562
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.544-275A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 5/14 | chr3 | 136283562 | ||||||
chr3:136283967
|
T | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0200others(21): Show | 25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.654+20T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136283967 | ||||||
chr3:136284316
|
T | TGATGTTT others(1): Show |
216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.654+369_654+370ins others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284316 | ||||||
chr3:136284317
|
T | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.654+370T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284317 | ||||||
chr3:136284352
|
A | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 49 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.654+405A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284352 | ||||||
chr3:136284363
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0123 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.654+416A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284363 | ||||||
chr3:136284750
|
A | C | 5 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+803A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284750 | ||||||
chr3:136284826
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0177others(1): Show | 4 | HG00738.hp1 HG01109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+879G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284826 | ||||||
chr3:136284854
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+907A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284854 | ||||||
chr3:136284871
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.654+924G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284871 | ||||||
chr3:136284892
|
G | A | 2 | a0002c0003t0001g0208a0002c0003t0001g0211 | 2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.654+945G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136284892 | ||||||
chr3:136285088
|
CA | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.654+1161delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285088 | |||||
chr3:136285088
|
CAA | C | 37 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(34): Show | 37 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.654+1160_654+1161d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285088 | |||||
chr3:136285104
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.654+1157A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285104 | ||||||
chr3:136285240
|
G | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(24): Show | 28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.654+1293G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285240 | ||||||
chr3:136285344
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.654+1397C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285344 | ||||||
chr3:136285463
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+1516A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136285463 | ||||||
chr3:136285552
|
G | GT | 10 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG02280.hp2 HG02738.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+1617dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285552 | |||||
chr3:136285966
|
A | ATTATAAA others(4): Show |
1 | a0001c0001t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.654+2024_654+2034d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136285966 | |||||
chr3:136286036
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.654+2089G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286036 | ||||||
chr3:136286073
|
A | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0176others(2): Show | 5 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+2126A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286073 | ||||||
chr3:136286083
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.654+2136C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286083 | ||||||
chr3:136286137
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.654+2190T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286137 | ||||||
chr3:136286784
|
G | A | 8 | a0001c0001t0001g0202a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | NA18943.hp2 NA18945.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+2837G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286784 | ||||||
chr3:136286904
|
G | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0046 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.654+2957G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286904 | ||||||
chr3:136286950
|
C | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 216 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.654+3003C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286950 | ||||||
chr3:136286962
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654+3015C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286962 | ||||||
chr3:136286986
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.654+3039G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136286986 | ||||||
chr3:136287038
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.654+3091A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287038 | ||||||
chr3:136287043
|
A | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.654+3096A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287043 | ||||||
chr3:136287045
|
A | AT | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.654+3098_654+3099i others(3): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287045 | ||||||
chr3:136287045
|
A | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(18): Show | 22 | HG00597.hp2 HG01106.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.654+3098A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287045 | ||||||
chr3:136287047
|
A | G | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+3100A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287047 | ||||||
chr3:136287047
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+3100A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287047 | ||||||
chr3:136287048
|
T | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+3101T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287048 | ||||||
chr3:136287060
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+3113C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287060 | ||||||
chr3:136287186
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+3239G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287186 | ||||||
chr3:136287389
|
TAGTA | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.654+3446_654+3449d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136287389 | |||||
chr3:136287439
|
G | GT | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG00544.hp1 HG00735.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.654+3502dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136287439 | |||||
chr3:136287527
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+3580G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287527 | ||||||
chr3:136287585
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.654+3638A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287585 | ||||||
chr3:136287734
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.654+3787T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287734 | ||||||
chr3:136287905
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.654+3958A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136287905 | ||||||
chr3:136288142
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.654+4195T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288142 | ||||||
chr3:136288176
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.654+4229T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288176 | ||||||
chr3:136288381
|
T | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+4434T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288381 | ||||||
chr3:136288415
|
A | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.654+4468A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288415 | ||||||
chr3:136288432
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0099 | 3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.654+4485G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288432 | ||||||
chr3:136288491
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.654+4544A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288491 | ||||||
chr3:136288576
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.654+4629C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288576 | ||||||
chr3:136288645
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.654+4698A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288645 | ||||||
chr3:136288646
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.654+4699T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288646 | ||||||
chr3:136288786
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.654+4839C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288786 | ||||||
chr3:136288789
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.654+4842G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288789 | ||||||
chr3:136288815
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.654+4868T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136288815 | ||||||
chr3:136289115
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.655-4641C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289115 | ||||||
chr3:136289138
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.655-4618A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289138 | ||||||
chr3:136289138
|
A | T | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655-4618A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289138 | ||||||
chr3:136289519
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-4237A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289519 | ||||||
chr3:136289556
|
A | G | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.655-4200A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289556 | ||||||
chr3:136289590
|
A | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0202a0001c0001t0001g0214others(41): Show | 45 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.655-4166A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289590 | ||||||
chr3:136289594
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.655-4162G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136289594 | ||||||
chr3:136289789
|
C | CT | 8 | a0001c0001t0001g0048a0001c0001t0001g0060a0001c0001t0001g0061others(5): Show | 8 | HG01070.hp1 HG01081.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-3958dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | |||||
chr3:136289789
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(3): Show | 6 | HG01243.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-3965_655-3958d others(10): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | |||||
chr3:136289789
|
C | CTTTTTTT others(2): Show |
41 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0019others(38): Show | 42 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.655-3966_655-3958d others(11): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | |||||
chr3:136289789
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0042others(5): Show | 8 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-3958_655-3957i others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | |||||
chr3:136289789
|
C | CTTTTTTT others(4): Show |
29 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(26): Show | 29 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.655-3958_655-3957i others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | |||||
chr3:136289789
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046others(2): Show | 5 | HG01069.hp2 HG01346.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.655-3958_655-3957i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136289789 | |||||
chr3:136290004
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.655-3752G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290004 | ||||||
chr3:136290068
|
A | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3688A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290068 | ||||||
chr3:136290102
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.655-3654A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290102 | ||||||
chr3:136290162
|
T | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.655-3594T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290162 | ||||||
chr3:136290250
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.655-3506G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290250 | ||||||
chr3:136290671
|
G | GTTTTTTT others(3): Show |
19 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0050others(16): Show | 20 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.655-3077_655-3068d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | |||||
chr3:136290671
|
G | GTTTTTTT others(4): Show |
194 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.655-3078_655-3068d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | |||||
chr3:136290671
|
G | GTTTTTTT others(5): Show |
66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(63): Show | 68 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.655-3079_655-3068d others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | |||||
chr3:136290671
|
G | GTTTTTTT others(6): Show |
9 | a0001c0001t0001g0007a0001c0001t0001g0079a0001c0001t0001g0137others(6): Show | 9 | HG00621.hp1 HG01346.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.655-3080_655-3068d others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | |||||
chr3:136290671
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.655-3081_655-3068d others(16): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136290671 | |||||
chr3:136290688
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.655-3068_655-3067i others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290688 | ||||||
chr3:136290688
|
T | TTTTTTTT others(6): Show |
1 | a0001c0001t0001g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-3068_655-3067i others(15): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290688 | ||||||
chr3:136290748
|
A | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0202a0001c0001t0001g0203others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.655-3008A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290748 | ||||||
chr3:136290757
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-2999A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290757 | ||||||
chr3:136290842
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.655-2914C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136290842 | ||||||
chr3:136291480
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.655-2276G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291480 | ||||||
chr3:136291539
|
CCTCTGAA others(4): Show |
C | 6 | a0001c0001t0001g0063a0001c0001t0001g0125a0001c0001t0001g0127others(3): Show | 6 | HG01943.hp2 HG02300.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-2216_655-2206d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291539 | ||||||
chr3:136291628
|
T | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(26): Show | 30 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.655-2128T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291628 | ||||||
chr3:136291774
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.655-1982G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291774 | ||||||
chr3:136291898
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.655-1858A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291898 | ||||||
chr3:136291908
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0044others(1): Show | 4 | HG01496.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-1848G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136291908 | ||||||
chr3:136292051
|
G | A | 2 | a0002c0003t0001g0208a0002c0003t0001g0211 | 2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.655-1705G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292051 | ||||||
chr3:136292160
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.655-1596T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292160 | ||||||
chr3:136292230
|
T | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0127a0001c0001t0001g0129others(2): Show | 5 | HG01943.hp2 HG02300.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-1526T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292230 | ||||||
chr3:136292236
|
G | GT | 54 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(51): Show | 54 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.655-1506dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136292236 | |||||
chr3:136292236
|
GT | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-1506delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 136292236 | |||||
chr3:136292287
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655-1469A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292287 | ||||||
chr3:136292395
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.655-1361A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292395 | ||||||
chr3:136292402
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.655-1354A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292402 | ||||||
chr3:136292535
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-1221A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292535 | ||||||
chr3:136292564
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.655-1192C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292564 | ||||||
chr3:136292778
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.655-978A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292778 | ||||||
chr3:136292993
|
C | A | 10 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0094others(7): Show | 10 | HG00621.hp2 HG02080.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-763C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136292993 | ||||||
chr3:136293009
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-747T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293009 | ||||||
chr3:136293379
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-377T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293379 | ||||||
chr3:136293513
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-243A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293513 | ||||||
chr3:136293551
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-205T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 6/14 | chr3 | 136293551 | ||||||
chr3:136293921
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.763+57C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136293921 | ||||||
chr3:136294075
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+211C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294075 | ||||||
chr3:136294108
|
A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.763+244A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294108 | ||||||
chr3:136294187
|
TTTATC | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+328_763+332del others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 136294187 | |||||
chr3:136294254
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.763+390A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294254 | ||||||
chr3:136294279
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.763+415A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294279 | ||||||
chr3:136294320
|
C | CT | 7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.763+465dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 136294320 | |||||
chr3:136294478
|
A | T | 1 | a0004c0005t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.763+614A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294478 | ||||||
chr3:136294702
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.763+838C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294702 | ||||||
chr3:136294720
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.763+856C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294720 | ||||||
chr3:136294857
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.763+993A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136294857 | ||||||
chr3:136295356
|
A | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0200others(21): Show | 25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.763+1492A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136295356 | ||||||
chr3:136295776
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.763+1912C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136295776 | ||||||
chr3:136295866
|
G | A | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.763+2002G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136295866 | ||||||
chr3:136296081
|
G | A | 14 | a0001c0001t0001g0047a0001c0001t0001g0201a0001c0001t0001g0212others(11): Show | 14 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.764-1871G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296081 | ||||||
chr3:136296089
|
A | G | 5 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-1863A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296089 | ||||||
chr3:136296242
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.764-1710C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296242 | ||||||
chr3:136296284
|
C | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-1668C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296284 | ||||||
chr3:136296291
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-1661A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296291 | ||||||
chr3:136296432
|
G | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(24): Show | 28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.764-1520G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296432 | ||||||
chr3:136296444
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.764-1508T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296444 | ||||||
chr3:136296581
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.764-1371A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296581 | ||||||
chr3:136296629
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.764-1323A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296629 | ||||||
chr3:136296931
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.764-1021C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136296931 | ||||||
chr3:136297020
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.764-932G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297020 | ||||||
chr3:136297317
|
T | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0272 | 2 | HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.764-635T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297317 | ||||||
chr3:136297429
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.764-523C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297429 | ||||||
chr3:136297444
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.764-508G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297444 | ||||||
chr3:136297494
|
T | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.764-458T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297494 | ||||||
chr3:136297516
|
T | C | 3 | a0001c0001t0001g0227a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG00280.hp1 HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.764-436T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297516 | ||||||
chr3:136297636
|
A | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(44): Show | 48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.764-316A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297636 | ||||||
chr3:136297817
|
T | C | 4 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0177others(1): Show | 4 | HG00738.hp1 HG01109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-135T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297817 | ||||||
chr3:136297926
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.764-26A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 7/14 | chr3 | 136297926 | ||||||
chr3:136298144
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.884+72C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298144 | ||||||
chr3:136298188
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG01167.hp1 HG01169.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.884+116G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298188 | ||||||
chr3:136298313
|
G | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.884+241G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298313 | ||||||
chr3:136298326
|
AT | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.884+260delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136298326 | |||||
chr3:136298333
|
G | C | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.884+261G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298333 | ||||||
chr3:136298353
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.884+281G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298353 | ||||||
chr3:136298458
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+386A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298458 | ||||||
chr3:136298754
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.884+682C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136298754 | ||||||
chr3:136299095
|
T | G | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.884+1023T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299095 | ||||||
chr3:136299098
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.884+1026C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299098 | ||||||
chr3:136299197
|
CAT | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.884+1132_884+1133d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299197 | |||||
chr3:136299208
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.884+1136A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299208 | ||||||
chr3:136299235
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.884+1163C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299235 | ||||||
chr3:136299299
|
T | C | 35 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(32): Show | 35 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.884+1227T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299299 | ||||||
chr3:136299318
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.884+1246G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299318 | ||||||
chr3:136299438
|
ATATATGC others(5): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1370_884+1381d others(14): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299438 | |||||
chr3:136299450
|
GTATGCAT others(109): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.884+1472_885-1371d others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299450 | |||||
chr3:136299458
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1386G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299458 | ||||||
chr3:136299460
|
G | GTATGTAT others(23): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0272 | 2 | HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.884+1393_884+1422d others(32): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299460 | |||||
chr3:136299462
|
ATGTATAG others(69): Show |
A | 73 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 74 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.884+1472_885-1411d others(78): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299462 | |||||
chr3:136299469
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1397G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299469 | ||||||
chr3:136299476
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1404A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299476 | ||||||
chr3:136299478
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1406G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299478 | ||||||
chr3:136299478
|
GTGTATGT others(73): Show |
G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.884+1416_885-1463d others(82): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299478 | |||||
chr3:136299484
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1412G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299484 | ||||||
chr3:136299489
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1417T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299489 | ||||||
chr3:136299494
|
GCATGTGT others(145): Show |
G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884+1423_885-1384d others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299494 | ||||||
chr3:136299502
|
A | ATGTATAG others(105): Show |
3 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG01167.hp1 HG01169.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.884+1436_885-1411d others(114): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299502 | |||||
chr3:136299510
|
GTATGCAT others(13): Show |
G | 2 | a0001c0001t0001g0006a0001c0001t0001g0205 | 3 | HG02109.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.884+1452_884+1471d others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299510 | |||||
chr3:136299538
|
G | GTGTA | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.884+1468_884+1471d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | |||||
chr3:136299538
|
G | GTGTATAG others(33): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0062 | 2 | HG00741.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.885-1312_885-1273d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | |||||
chr3:136299538
|
G | GTGTATAG others(73): Show |
1 | a0001c0001t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.885-1352_885-1273d others(82): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | |||||
chr3:136299538
|
GTGTATAG others(33): Show |
G | 2 | a0001c0001t0001g0221a0001c0001t0001g0287 | 2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.885-1312_885-1273d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299538 | |||||
chr3:136299558
|
A | ATGTATGT others(31): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.885-1470_885-1433d others(40): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299558 | |||||
chr3:136299578
|
A | ATGTATAG others(65): Show |
1 | a0001c0001t0001g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.885-1411_885-1410i others(74): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299578 | |||||
chr3:136299598
|
A | ATGTATGT others(105): Show |
1 | a0001c0001t0001g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.885-1411_885-1410i others(114): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299598 | |||||
chr3:136299598
|
A | ATGTATGT others(109): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG00544.hp1 NA18954.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.885-1422_885-1307d others(118): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299598 | |||||
chr3:136299606
|
ATATGCAT others(13): Show |
A | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.885-1406_885-1387d others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299606 | |||||
chr3:136299634
|
GTGTA | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | NA18959.hp1 NA18973.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.885-1386_885-1383d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299634 | |||||
chr3:136299646
|
A | ATATGCAT others(13): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0220 | 2 | HG01496.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.885-1366_885-1347d others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299646 | |||||
chr3:136299678
|
A | G | 11 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0166others(8): Show | 11 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.885-1352A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299678 | ||||||
chr3:136299697
|
T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(44): Show | 48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.885-1333T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299697 | ||||||
chr3:136299718
|
A | ATGTATGT others(33): Show |
4 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0104others(1): Show | 4 | NA18943.hp1 NA18965.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-1301_885-1262d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299718 | |||||
chr3:136299732
|
ATGTGTAT others(17): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1272_885-1249d others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299732 | |||||
chr3:136299739
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.885-1291T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299739 | ||||||
chr3:136299756
|
G | GTATGTAT others(165): Show |
1 | a0001c0001t0001g0007 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.885-1273_885-1272i others(174): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | |||||
chr3:136299756
|
G | GTATGTAT others(9): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG00544.hp1 NA18954.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.885-1273_885-1272i others(18): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | |||||
chr3:136299756
|
G | GTATGTAT others(29): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.885-1273_885-1272i others(38): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | |||||
chr3:136299756
|
G | GTATGTAT others(229): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.885-1273_885-1272i others(238): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299756 | |||||
chr3:136299768
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.885-1262A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299768 | ||||||
chr3:136299782
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.885-1248A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299782 | ||||||
chr3:136299809
|
GGTATGCA others(33): Show |
G | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.885-1219_885-1180d others(42): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299809 | |||||
chr3:136299849
|
T | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-1181T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299849 | ||||||
chr3:136299850
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1180G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299850 | ||||||
chr3:136299851
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-1179C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299851 | ||||||
chr3:136299878
|
G | GTGTATGT others(13): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-1144_885-1143i others(22): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136299878 | |||||
chr3:136299880
|
G | T | 1 | a0001c0001t0001g0288 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.885-1150G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299880 | ||||||
chr3:136299887
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1143C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299887 | ||||||
chr3:136299917
|
T | C | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | NA18959.hp1 NA18973.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.885-1113T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299917 | ||||||
chr3:136299966
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-1064G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136299966 | ||||||
chr3:136300007
|
CAT | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0161a0001c0001t0001g0167 | 4 | HG01884.hp2 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.885-1020_885-1019d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136300007 | |||||
chr3:136300008
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0287 | 2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.885-1022A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300008 | ||||||
chr3:136300023
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 7 | HG01243.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-1007C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300023 | ||||||
chr3:136300065
|
AACACATA others(19): Show |
A | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-955_885-930del others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136300065 | |||||
chr3:136300071
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.885-959T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300071 | ||||||
chr3:136300116
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.885-914A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300116 | ||||||
chr3:136300152
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-878A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300152 | ||||||
chr3:136300169
|
T | TGTATAA | 88 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 89 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.885-856_885-855ins others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 136300169 | |||||
chr3:136300193
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.885-837A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300193 | ||||||
chr3:136300276
|
G | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.885-754G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300276 | ||||||
chr3:136300362
|
A | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.885-668A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300362 | ||||||
chr3:136300847
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.885-183C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300847 | ||||||
chr3:136300998
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.885-32G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 8/14 | chr3 | 136300998 | ||||||
chr3:136301265
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.966+154T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301265 | ||||||
chr3:136301316
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+205G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301316 | ||||||
chr3:136301400
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+289G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301400 | ||||||
chr3:136301453
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+342T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301453 | ||||||
chr3:136301555
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.966+444G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301555 | ||||||
chr3:136301612
|
C | T | 15 | a0001c0001t0001g0047a0001c0001t0001g0201a0001c0001t0001g0212others(12): Show | 15 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.966+501C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301612 | ||||||
chr3:136301699
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.966+588T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301699 | ||||||
chr3:136301732
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+621A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301732 | ||||||
chr3:136301769
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+658T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301769 | ||||||
chr3:136301891
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+780A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136301891 | ||||||
chr3:136302103
|
A | C | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.966+992A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302103 | ||||||
chr3:136302106
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.966+995A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302106 | ||||||
chr3:136302133
|
A | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.966+1022A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302133 | ||||||
chr3:136302162
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.966+1051C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302162 | ||||||
chr3:136302171
|
CTCCTGCA others(5178): Show |
C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(104): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.966+1061_966+6245d others(2): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302171 | ||||||
chr3:136302210
|
C | A | 12 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0148others(9): Show | 12 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+1099C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302210 | ||||||
chr3:136302238
|
G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+1127G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302238 | ||||||
chr3:136302354
|
G | T | 1 | a0001c0001t0001g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.966+1243G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302354 | ||||||
chr3:136302477
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+1366T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302477 | ||||||
chr3:136302583
|
C | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.966+1472C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302583 | ||||||
chr3:136302690
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+1579A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302690 | ||||||
chr3:136302805
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0214 | 3 | HG01070.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.966+1694C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302805 | ||||||
chr3:136302957
|
G | A | 5 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+1846G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136302957 | ||||||
chr3:136303001
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.966+1890T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303001 | ||||||
chr3:136303459
|
C | G | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.966+2348C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303459 | ||||||
chr3:136303527
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+2416T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303527 | ||||||
chr3:136303570
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.966+2459C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303570 | ||||||
chr3:136303571
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0155 | 3 | HG00280.hp2 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.966+2460G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303571 | ||||||
chr3:136303603
|
T | A | 7 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(4): Show | 7 | NA18951.hp2 NA18952.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.966+2492T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303603 | ||||||
chr3:136303986
|
T | TA | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+2875_966+2876i others(3): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136303986 | ||||||
chr3:136304150
|
C | CT | 6 | a0001c0001t0001g0147a0001c0001t0001g0156a0001c0001t0001g0157others(3): Show | 6 | HG01175.hp1 HG01346.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3055dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136304150 | |||||
chr3:136304150
|
CT | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG00544.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3055delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136304150 | |||||
chr3:136304194
|
A | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0176others(2): Show | 5 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+3083A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304194 | ||||||
chr3:136304253
|
C | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+3142C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304253 | ||||||
chr3:136304371
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+3260C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304371 | ||||||
chr3:136304383
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.966+3272T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304383 | ||||||
chr3:136304386
|
A | AT | 24 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(21): Show | 25 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.966+3278dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136304386 | |||||
chr3:136304390
|
A | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 88 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.966+3279A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304390 | ||||||
chr3:136304403
|
T | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.966+3292T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304403 | ||||||
chr3:136304420
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0033 | 2 | HG02015.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.966+3309C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304420 | ||||||
chr3:136304443
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.966+3332G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304443 | ||||||
chr3:136304525
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.966+3414G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304525 | ||||||
chr3:136304627
|
T | C | 15 | a0001c0001t0001g0047a0001c0001t0001g0201a0001c0001t0001g0212others(12): Show | 15 | HG00099.hp2 HG01074.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.966+3516T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304627 | ||||||
chr3:136304826
|
T | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+3715T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304826 | ||||||
chr3:136304848
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0202a0001c0001t0001g0203others(41): Show | 45 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.966+3737C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304848 | ||||||
chr3:136304958
|
G | A | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.966+3847G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304958 | ||||||
chr3:136304982
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.966+3871C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304982 | ||||||
chr3:136304999
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.966+3888C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136304999 | ||||||
chr3:136305001
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3890A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305001 | ||||||
chr3:136305155
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+4044C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305155 | ||||||
chr3:136305255
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.966+4144T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305255 | ||||||
chr3:136305379
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.966+4268A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305379 | ||||||
chr3:136305519
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+4408C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305519 | ||||||
chr3:136305691
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.966+4580A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305691 | ||||||
chr3:136305746
|
T | TA | 29 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0118others(26): Show | 30 | HG00544.hp1 HG00738.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.966+4650dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136305746 | |||||
chr3:136305746
|
TA | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(19): Show | 22 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.966+4650delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136305746 | |||||
chr3:136305762
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+4651G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305762 | ||||||
chr3:136305802
|
G | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+4691G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305802 | ||||||
chr3:136305816
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.966+4705T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305816 | ||||||
chr3:136305888
|
A | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+4777A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136305888 | ||||||
chr3:136306214
|
G | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+5103G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136306214 | ||||||
chr3:136306477
|
A | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(24): Show | 28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.966+5366A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136306477 | ||||||
chr3:136307090
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0269a0001c0001t0001g0274 | 3 | HG02976.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.966+5979G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307090 | ||||||
chr3:136307350
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.966+6239G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307350 | ||||||
chr3:136307357
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(104): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.966+6246G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307357 | ||||||
chr3:136307438
|
T | G | 1 | a0001c0001t0001g0283 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+6327T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307438 | ||||||
chr3:136307439
|
C | A | 1 | a0001c0001t0001g0283 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+6328C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307439 | ||||||
chr3:136307442
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+6331C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307442 | ||||||
chr3:136307642
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+6531G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307642 | ||||||
chr3:136307688
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0099 | 3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.966+6577A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307688 | ||||||
chr3:136307747
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+6636G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307747 | ||||||
chr3:136307889
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.966+6778C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136307889 | ||||||
chr3:136307977
|
A | AAAT | 37 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(34): Show | 38 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.966+6889_966+6891d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136307977 | |||||
chr3:136307977
|
A | AAATAATA others(2): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+6883_966+6891d others(11): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136307977 | |||||
chr3:136307977
|
AAATAAT | A | 30 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(27): Show | 30 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.966+6886_966+6891d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136307977 | |||||
chr3:136308025
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.966+6914C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308025 | ||||||
chr3:136308191
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0044others(1): Show | 4 | HG01496.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+7080T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308191 | ||||||
chr3:136308234
|
C | CT | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.966+7140dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136308234 | |||||
chr3:136308234
|
C | CTT | 6 | a0001c0001t0001g0095a0001c0001t0001g0117a0001c0001t0001g0138others(3): Show | 6 | HG02074.hp1 HG06807.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+7139_966+7140d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136308234 | |||||
chr3:136308303
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.966+7192A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308303 | ||||||
chr3:136308493
|
G | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+7382G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308493 | ||||||
chr3:136308707
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.966+7596A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308707 | ||||||
chr3:136308798
|
G | A | 43 | a0001c0001t0001g0005a0001c0001t0001g0202a0001c0001t0001g0214others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.966+7687G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136308798 | ||||||
chr3:136309055
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-7886G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309055 | ||||||
chr3:136309092
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.967-7849G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309092 | ||||||
chr3:136309151
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.967-7790T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309151 | ||||||
chr3:136309166
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.967-7775G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309166 | ||||||
chr3:136309212
|
C | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-7729C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309212 | ||||||
chr3:136309262
|
C | CA | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0061others(4): Show | 7 | HG02280.hp2 HG02300.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-7661dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136309262 | |||||
chr3:136309262
|
CA | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG00544.hp1 HG01169.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.967-7661delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136309262 | |||||
chr3:136309486
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-7455T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309486 | ||||||
chr3:136309659
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG01243.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-7282G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309659 | ||||||
chr3:136309801
|
CA | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(5): Show | 9 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.967-7126delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136309801 | |||||
chr3:136309998
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.967-6943A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136309998 | ||||||
chr3:136310114
|
C | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.967-6827C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310114 | ||||||
chr3:136310145
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(100): Show | 105 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.967-6796C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310145 | ||||||
chr3:136310193
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-6748G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310193 | ||||||
chr3:136310295
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.967-6646G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310295 | ||||||
chr3:136310303
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.967-6638C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310303 | ||||||
chr3:136310318
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-6623G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310318 | ||||||
chr3:136310351
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-6590G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310351 | ||||||
chr3:136310397
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0254 | 3 | NA18952.hp2 NA19082.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.967-6544C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310397 | ||||||
chr3:136310416
|
G | C | 32 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046others(29): Show | 32 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.967-6525G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310416 | ||||||
chr3:136310422
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.967-6519C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310422 | ||||||
chr3:136310515
|
C | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0270 | 2 | HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.967-6426C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310515 | ||||||
chr3:136310618
|
TAGAAAGT others(17): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.967-6321_967-6298d others(26): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136310618 | |||||
chr3:136310647
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.967-6294T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310647 | ||||||
chr3:136310724
|
T | G | 5 | a0001c0001t0001g0204a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.967-6217T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310724 | ||||||
chr3:136310769
|
C | G | 5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG00609.hp1 HG01884.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-6172C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310769 | ||||||
chr3:136310881
|
T | C | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.967-6060T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310881 | ||||||
chr3:136310900
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.967-6041G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136310900 | ||||||
chr3:136311074
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.967-5867C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311074 | ||||||
chr3:136311205
|
G | T | 1 | a0001c0001t0001g0014 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.967-5736G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311205 | ||||||
chr3:136311348
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.967-5593T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311348 | ||||||
chr3:136311443
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-5498C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311443 | ||||||
chr3:136311450
|
A | G | 1 | a0007c0006t0001g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.967-5491A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311450 | ||||||
chr3:136311454
|
A | G | 1 | a0005c0008t0001g0230 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.967-5487A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311454 | ||||||
chr3:136311510
|
A | AT | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-5420dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136311510 | |||||
chr3:136311559
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-5382C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311559 | ||||||
chr3:136311604
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG00738.hp2 HG01106.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-5337T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311604 | ||||||
chr3:136311918
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.967-5023C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136311918 | ||||||
chr3:136312175
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-4766G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312175 | ||||||
chr3:136312316
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.967-4625C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312316 | ||||||
chr3:136312516
|
G | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.967-4425G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312516 | ||||||
chr3:136312636
|
T | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0176others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-4305T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312636 | ||||||
chr3:136312851
|
G | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0290 | 2 | NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.967-4090G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312851 | ||||||
chr3:136312939
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-4002C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136312939 | ||||||
chr3:136313082
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.967-3859C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313082 | ||||||
chr3:136313207
|
G | A | 6 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG00280.hp2 HG01081.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-3734G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313207 | ||||||
chr3:136313253
|
G | A | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-3688G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313253 | ||||||
chr3:136313356
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.967-3585A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313356 | ||||||
chr3:136313472
|
CA | C | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-3467delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136313472 | |||||
chr3:136313483
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-3458G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313483 | ||||||
chr3:136313644
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.967-3297A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313644 | ||||||
chr3:136313820
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0046 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.967-3121T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136313820 | ||||||
chr3:136314032
|
T | TCA | 36 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(33): Show | 36 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.967-2894_967-2893d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136314032 | |||||
chr3:136314032
|
T | TCACA | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-2896_967-2893d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136314032 | |||||
chr3:136314186
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.967-2755A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136314186 | ||||||
chr3:136314439
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.967-2502G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136314439 | ||||||
chr3:136314483
|
T | G | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.967-2458T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136314483 | ||||||
chr3:136314672
|
AAACAAAA others(4): Show |
A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-2266_967-2256d others(13): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136314672 | |||||
chr3:136315109
|
T | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1832T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315109 | ||||||
chr3:136315110
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1831A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315110 | ||||||
chr3:136315161
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1780A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315161 | ||||||
chr3:136315264
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.967-1677G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315264 | ||||||
chr3:136315274
|
A | G | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1667A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315274 | ||||||
chr3:136315313
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.967-1628G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315313 | ||||||
chr3:136315331
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.967-1610C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315331 | ||||||
chr3:136315365
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.967-1576C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315365 | ||||||
chr3:136315458
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG00280.hp1 HG00323.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.967-1483C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315458 | ||||||
chr3:136315613
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.967-1328G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315613 | ||||||
chr3:136315648
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.967-1293T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315648 | ||||||
chr3:136315661
|
T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(44): Show | 48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.967-1280T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315661 | ||||||
chr3:136315678
|
A | AT | 9 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 9 | HG00099.hp1 HG00733.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.967-1251dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136315678 | |||||
chr3:136315879
|
C | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0116a0001c0001t0001g0122others(1): Show | 4 | HG00423.hp2 NA18963.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-1062C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315879 | ||||||
chr3:136315899
|
G | C | 8 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG00280.hp2 HG01081.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-1042G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315899 | ||||||
chr3:136315911
|
T | TTA | 46 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 47 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.967-1019_967-1018d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136315911 | |||||
chr3:136315925
|
AAGAG | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-1011_967-1008d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136315925 | |||||
chr3:136315969
|
C | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0099 | 3 | NA18974.hp2 NA18977.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.967-972C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136315969 | ||||||
chr3:136316006
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.967-935G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316006 | ||||||
chr3:136316181
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-760C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316181 | ||||||
chr3:136316184
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-757C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316184 | ||||||
chr3:136316226
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.967-715A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316226 | ||||||
chr3:136316227
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.967-714G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316227 | ||||||
chr3:136316227
|
G | GA | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.967-701dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 136316227 | |||||
chr3:136316277
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(44): Show | 48 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.967-664G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316277 | ||||||
chr3:136316363
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-578T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316363 | ||||||
chr3:136316375
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.967-566G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316375 | ||||||
chr3:136316461
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.967-480C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316461 | ||||||
chr3:136316489
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-452C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316489 | ||||||
chr3:136316895
|
A | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 83 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.967-46A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316895 | ||||||
chr3:136316899
|
G | C | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.967-42G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 9/14 | chr3 | 136316899 | ||||||
chr3:136317212
|
A | AT | 59 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0022others(56): Show | 60 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1090+178dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
A | ATT | 18 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0034others(15): Show | 18 | HG00423.hp1 HG00738.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1090+177_1090+178d others(4): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
A | ATTT | 14 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0122others(11): Show | 15 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1090+176_1090+178d others(5): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
A | ATTTT | 57 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0050others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1090+175_1090+178d others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
A | ATTTTT | 33 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0043others(30): Show | 34 | HG00609.hp1 HG00621.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1090+174_1090+178d others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
A | ATTTTTT | 6 | a0001c0001t0001g0066a0001c0001t0001g0081a0001c0001t0001g0088others(3): Show | 6 | HG00423.hp2 HG01123.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+173_1090+178d others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
AT | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0036others(9): Show | 12 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1090+178delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
ATTTTTTT | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 27 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.1090+172_1090+178d others(9): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317212
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0160 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1090+169_1090+178d others(12): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136317212 | |||||
chr3:136317265
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+201A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317265 | ||||||
chr3:136317347
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1090+283G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317347 | ||||||
chr3:136317358
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+294A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317358 | ||||||
chr3:136317384
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 203 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1090+320A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317384 | ||||||
chr3:136317387
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1090+323A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317387 | ||||||
chr3:136317494
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02280.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1090+430G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317494 | ||||||
chr3:136317846
|
G | A | 7 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(4): Show | 7 | NA18951.hp2 NA18952.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1090+782G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136317846 | ||||||
chr3:136318144
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1090+1080T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318144 | ||||||
chr3:136318215
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1090+1151C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318215 | ||||||
chr3:136318226
|
T | TC | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+1164dupC | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136318226 | |||||
chr3:136318287
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1090+1223T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318287 | ||||||
chr3:136318328
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1090+1264T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318328 | ||||||
chr3:136318385
|
A | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(110): Show | 115 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1090+1321A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318385 | ||||||
chr3:136318386
|
A | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0103 | 3 | HG01123.hp1 NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1090+1322A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318386 | ||||||
chr3:136318659
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1090+1595C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318659 | ||||||
chr3:136318696
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+1632C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318696 | ||||||
chr3:136318768
|
ATAT | A | 6 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+1708_1090+171 others(7): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136318768 | |||||
chr3:136318865
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(109): Show | 114 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1090+1801G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318865 | ||||||
chr3:136318882
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0130 | 2 | NA19058.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1090+1818A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318882 | ||||||
chr3:136318900
|
C | T | 4 | a0001c0001t0001g0201a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG00099.hp2 HG01168.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090+1836C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318900 | ||||||
chr3:136318925
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+1861G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136318925 | ||||||
chr3:136319097
|
G | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1090+2033G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319097 | ||||||
chr3:136319125
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046 | 3 | HG01433.hp1 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1090+2061A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319125 | ||||||
chr3:136319160
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1090+2096A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319160 | ||||||
chr3:136319209
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1090+2145C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319209 | ||||||
chr3:136319356
|
C | T | 9 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0150others(6): Show | 9 | HG00280.hp2 HG01081.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1090+2292C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319356 | ||||||
chr3:136319386
|
A | AT | 30 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0068others(27): Show | 31 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1090+2338dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136319386 | |||||
chr3:136319386
|
A | ATT | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG01123.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1090+2337_1090+233 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136319386 | |||||
chr3:136319453
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0270 | 2 | HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1090+2389A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319453 | ||||||
chr3:136319460
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+2396G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319460 | ||||||
chr3:136319483
|
G | T | 1 | a0001c0001t0001g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1090+2419G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319483 | ||||||
chr3:136319522
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1090+2458C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319522 | ||||||
chr3:136319564
|
ATTTTTGT others(28): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1090+2501_1090+253 others(39): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319564 | ||||||
chr3:136319579
|
G | A | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1090+2515G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319579 | ||||||
chr3:136319600
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1090+2536G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319600 | ||||||
chr3:136319617
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+2553C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319617 | ||||||
chr3:136319732
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1090+2668G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319732 | ||||||
chr3:136319767
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1090+2703G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319767 | ||||||
chr3:136319834
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1090+2770G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319834 | ||||||
chr3:136319895
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1090+2831T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319895 | ||||||
chr3:136319941
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+2877G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136319941 | ||||||
chr3:136320146
|
A | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1090+3082A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320146 | ||||||
chr3:136320200
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1090+3136A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320200 | ||||||
chr3:136320426
|
C | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(105): Show | 110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1090+3362C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320426 | ||||||
chr3:136320578
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1090+3514G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320578 | ||||||
chr3:136320648
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090+3584T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320648 | ||||||
chr3:136320798
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(26): Show | 30 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1090+3734C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320798 | ||||||
chr3:136320801
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(26): Show | 30 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1090+3737A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320801 | ||||||
chr3:136320971
|
C | A | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1090+3907C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136320971 | ||||||
chr3:136321146
|
G | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1090+4082G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321146 | ||||||
chr3:136321249
|
A | C | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1090+4185A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321249 | ||||||
chr3:136321546
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1090+4482G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321546 | ||||||
chr3:136321601
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1090+4537C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321601 | ||||||
chr3:136321728
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(8): Show | 11 | HG00544.hp1 HG01243.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1090+4664C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321728 | ||||||
chr3:136321740
|
G | C | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1090+4676G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321740 | ||||||
chr3:136321883
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1090+4819G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321883 | ||||||
chr3:136321922
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0046 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1090+4858T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321922 | ||||||
chr3:136321929
|
A | T | 5 | a0001c0001t0001g0202a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | NA18953.hp2 NA18964.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090+4865A>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321929 | ||||||
chr3:136321957
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0055others(4): Show | 7 | HG01123.hp1 NA18948.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-4846A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136321957 | ||||||
chr3:136322215
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0274 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1091-4588G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322215 | ||||||
chr3:136322681
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1091-4122C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322681 | ||||||
chr3:136322726
|
G | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG02135.hp2 NA18747.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-4077G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322726 | ||||||
chr3:136322741
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1091-4062C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322741 | ||||||
chr3:136322914
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-3889A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136322914 | ||||||
chr3:136322998
|
GT | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(232): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1091-3787delT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136322998 | |||||
chr3:136322998
|
GTT | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(35): Show | 39 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.1091-3788_1091-378 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136322998 | |||||
chr3:136323005
|
T | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(2): Show | 5 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1091-3798T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323005 | ||||||
chr3:136323006
|
T | G | 1 | a0001c0001t0001g0009 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1091-3797T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323006 | ||||||
chr3:136323079
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp2 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1091-3724T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323079 | ||||||
chr3:136323126
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1091-3677G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323126 | ||||||
chr3:136323313
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0161a0001c0001t0001g0167 | 4 | HG01884.hp2 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-3490A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323313 | ||||||
chr3:136323322
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(78): Show | 82 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.1091-3481T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323322 | ||||||
chr3:136323543
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091-3260A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323543 | ||||||
chr3:136323590
|
C | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-3213C>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323590 | ||||||
chr3:136323641
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1091-3162C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323641 | ||||||
chr3:136323714
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1091-3089G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323714 | ||||||
chr3:136323774
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091-3029A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323774 | ||||||
chr3:136323807
|
C | CA | 40 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(37): Show | 41 | HG00621.hp1 HG00642.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1091-2980dupA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323807 | |||||
chr3:136323807
|
C | CAA | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(9): Show | 12 | HG00544.hp1 HG01175.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1091-2981_1091-298 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323807 | |||||
chr3:136323807
|
CA | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0111a0001c0001t0001g0197others(3): Show | 6 | HG01106.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1091-2980delA | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323807 | |||||
chr3:136323877
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1091-2926C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323877 | ||||||
chr3:136323899
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0171 | 2 | HG01255.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1091-2904T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323899 | ||||||
chr3:136323957
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0034 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1091-2846G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136323957 | ||||||
chr3:136323992
|
G | GT | 9 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0034others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1091-2797dupT | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136323992 | |||||
chr3:136324064
|
C | CTG | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091-2738_1091-273 others(6): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136324064 | |||||
chr3:136324505
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1091-2298C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324505 | ||||||
chr3:136324506
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1091-2297G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324506 | ||||||
chr3:136324550
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 53 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1091-2253T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324550 | ||||||
chr3:136324663
|
G | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1091-2140G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324663 | ||||||
chr3:136324756
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0119others(24): Show | 28 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.1091-2047G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324756 | ||||||
chr3:136324954
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1091-1849A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324954 | ||||||
chr3:136324986
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1091-1817A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136324986 | ||||||
chr3:136325041
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1091-1762C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325041 | ||||||
chr3:136325046
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1091-1757C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325046 | ||||||
chr3:136325097
|
C | G | 1 | a0001c0001t0001g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1091-1706C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325097 | ||||||
chr3:136325292
|
G | GGGAC | 3 | a0001c0001t0001g0047a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | NA18946.hp2 NA19060.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1091-1510_1091-150 others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136325292 | |||||
chr3:136325390
|
TCTCA | T | 21 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(18): Show | 21 | HG00280.hp2 HG00733.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1091-1409_1091-140 others(8): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136325390 | |||||
chr3:136325513
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1091-1290C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325513 | ||||||
chr3:136325609
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0232 | 3 | HG02080.hp1 NA18986.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1091-1194G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325609 | ||||||
chr3:136325651
|
C | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1091-1152C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325651 | ||||||
chr3:136325801
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1091-1002C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325801 | ||||||
chr3:136325844
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-959T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325844 | ||||||
chr3:136325963
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-840G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136325963 | ||||||
chr3:136326087
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-716C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326087 | ||||||
chr3:136326209
|
TG | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-592delG | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 136326209 | |||||
chr3:136326273
|
C | G | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091-530C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326273 | ||||||
chr3:136326371
|
G | A | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1091-432G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326371 | ||||||
chr3:136326382
|
G | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-421G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326382 | ||||||
chr3:136326431
|
G | A | 4 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG03139.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091-372G>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326431 | ||||||
chr3:136326787
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1091-16A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 10/14 | chr3 | 136326787 | ||||||
chr3:136327909
|
T | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1398+177T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136327909 | ||||||
chr3:136327934
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0255 | 2 | NA18951.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1398+202C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136327934 | ||||||
chr3:136327970
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0205a0001c0001t0001g0262others(4): Show | 8 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1398+238C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136327970 | ||||||
chr3:136328066
|
T | A | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1398+334T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328066 | ||||||
chr3:136328339
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1399-419C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328339 | ||||||
chr3:136328347
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(109): Show | 114 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1399-411A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328347 | ||||||
chr3:136328458
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-300A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328458 | ||||||
chr3:136328535
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1399-223T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328535 | ||||||
chr3:136328540
|
G | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1399-218G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328540 | ||||||
chr3:136328546
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1399-212G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 13/14 | chr3 | 136328546 | ||||||
chr3:136329074
|
T | TAACACCA others(32): Show |
1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+217_1498+218i others(41): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329074 | ||||||
chr3:136329075
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+218T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329075 | ||||||
chr3:136329078
|
ATTTCTAG others(28): Show |
A | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+222_1498+256d others(37): Show |
PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329078 | ||||||
chr3:136329089
|
T | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00544.hp1 HG02135.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1498+232T>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329089 | ||||||
chr3:136329097
|
G | T | 1 | a0001c0001t0003g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1498+240G>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329097 | ||||||
chr3:136329135
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1498+278A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329135 | ||||||
chr3:136329157
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+300T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329157 | ||||||
chr3:136329166
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+309G>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329166 | ||||||
chr3:136329168
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+311T>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329168 | ||||||
chr3:136329169
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+312T>A | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329169 | ||||||
chr3:136329170
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1498+313A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329170 | ||||||
chr3:136329333
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1498+476C>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329333 | ||||||
chr3:136329358
|
A | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG00544.hp1 HG02135.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498+501A>C | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329358 | ||||||
chr3:136329676
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1499-229C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329676 | ||||||
chr3:136329860
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1499-45A>G | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329860 | ||||||
chr3:136329885
|
C | T | 2 | a0001c0001t0001g0085a0003c0004t0001g0083 | 2 | NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1499-20C>T | PCCB | ENSG00000114054.14 | transcript | ENST00000251654.9 | protein_coding | 14/14 | chr3 | 136329885 |