geneid | 79886 |
---|---|
ensemblid | ENSG00000120159.13 |
hgncid | 25834 |
symbol | CAAP1 |
name | caspase activity and apoptosis inhibitor 1 |
refseq_nuc | NM_024828.4 |
refseq_prot | NP_079104.3 |
ensembl_nuc | ENST00000333916.8 |
ensembl_prot | ENSP00000369431.3 |
mane_status | MANE Select |
chr | chr9 |
start | 26840685 |
end | 26892802 |
strand | - |
ver | v1.2 |
region | chr9:26840685-26892802 |
region5000 | chr9:26835685-26897802 |
regionname0 | CAAP1_chr9_26840685_26892802 |
regionname5000 | CAAP1_chr9_26835685_26897802 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 361 | 344 | 64 | 68 | 155 | 18 | 37 | 116 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0002 | 0/0 | 361 | 20 | 18 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0003 | 0/0 | 361 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0004 | 0/0 | 361 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0005 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0006 | 0/0 | 312 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0007 | 0/0 | 361 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1086 | 234 | 55 | 52 | 77 | 18 | 30 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0002 | 0/0 | 1086 | 110 | 9 | 16 | 78 | 0 | 7 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0003 | 0/0 | 1086 | 19 | 17 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0004 | 0/0 | 1086 | 3 | 3 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0005 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0006 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0007 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0008 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0009 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
c0010 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1704 | 317 | 72 | 47 | 150 | 14 | 32 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0002 | 0/0 | 1704 | 36 | 8 | 20 | 0 | 4 | 4 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0003 | 0/0 | 1704 | 3 | 0 | 3 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0004 | 0/0 | 1704 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0005 | 0/0 | 1704 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0006 | 0/0 | 1704 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0007 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0008 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0009 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0010 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0011 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0012 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0013 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0014 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0015 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
t0016 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1086 | 234 | 55 | 52 | 77 | 18 | 30 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0002 | 0/0 | 1086 | 110 | 9 | 16 | 78 | 0 | 7 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0002c0003 | 0/0 | 1086 | 19 | 17 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0002c0007 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0003c0004 | 0/0 | 1086 | 3 | 3 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0004c0008 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0004c0010 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0005c0005 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0006c0009 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0007c0006 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2789 | 183 | 42 | 29 | 73 | 14 | 23 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0002 | 0/0 | 2789 | 36 | 8 | 20 | 0 | 4 | 4 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0003 | 0/0 | 2789 | 3 | 0 | 3 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0004 | 0/0 | 2789 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0005 | 0/0 | 2789 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0006 | 0/0 | 2789 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0007 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0008 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0010 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0013 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0014 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0001t0016 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0002t0001 | 0/0 | 2789 | 109 | 9 | 16 | 77 | 0 | 7 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0001c0002t0012 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0002c0003t0001 | 0/0 | 2789 | 19 | 17 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0002c0007t0011 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0003c0004t0001 | 0/0 | 2789 | 3 | 3 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0004c0008t0001 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0004c0010t0015 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0005c0005t0009 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0006c0009t0001 | 0/0 | 2789 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
a0007c0006t0001 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | copy fasta | chr9 | 26835685 | 26897802 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0006g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0006g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0013g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0001t0016g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0001c0002t0012g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0002c0007t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0003c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0003c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0003c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0004c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0004c0010t0015g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0005c0005t0009g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0006c0009t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
a0007c0006t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0224 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0232 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | FIN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0131 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00558 | hp2 | a0005 | c0005 | t0009 | g0017 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0335 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | CHS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0341 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0342 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01496 | hp2 | a0002 | c0003 | t0001 | g0027 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01884 | hp1 | a0003 | c0004 | t0001 | g0097 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01891 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0327 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0338 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0339 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0347 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | CDX | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0036 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0271 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0354 | AMR | PEL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02451 | hp1 | a0003 | c0004 | t0001 | g0252 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02572 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02683 | hp1 | a0004 | c0010 | t0015 | g0331 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02683 | hp2 | a0001 | c0001 | t0013 | g0084 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0356 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0345 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0348 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0343 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0120 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02970 | hp1 | a0002 | c0003 | t0001 | g0022 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02976 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0349 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03041 | hp2 | a0002 | c0003 | t0001 | g0031 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0020 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0337 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0346 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0033 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03209 | hp2 | a0002 | c0003 | t0001 | g0032 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0035 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03540 | hp2 | a0007 | c0006 | t0001 | g0025 | AFR | GWD | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0300 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0262 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0352 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0281 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04184 | hp2 | a0001 | c0001 | t0016 | g0184 | SAS | BEB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04199 | hp2 | a0006 | c0009 | t0001 | g0139 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04228 | hp1 | a0004 | c0008 | t0001 | g0089 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG04228 | hp2 | a0001 | c0001 | t0007 | g0151 | SAS | STU | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18906 | hp1 | a0002 | c0003 | t0001 | g0029 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18975 | hp1 | a0001 | c0001 | t0008 | g0206 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19030 | hp1 | a0002 | c0007 | t0011 | g0026 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19030 | hp2 | a0003 | c0004 | t0001 | g0253 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19058 | hp2 | a0001 | c0002 | t0012 | g0315 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19080 | hp1 | a0001 | c0001 | t0014 | g0187 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0336 | AFR | ASW | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ASW | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0233 | EUR | TSI | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | GIH | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0355 | AFR | ACB | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | MSL | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
NA21309 | hp2 | a0002 | c0003 | t0001 | g0030 | AFR | LWK | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0150 | REF | REF | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0062 | REF | REF | CAAP1_chr9_26835685_26897802 | CAAP1 | chr9 | 26835685 | 26897802 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26842378
|
C | A | 1 | a0006 | 1 | HG04199.hp2 | stop_gained | HIGH | c.1009G>T | p.Glu337* | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1096/2789 | 1009/1086 | 337/361 | chr9 | 26842378 | ||
chr9:26842384
|
G | A | 1 | a0006 | 1 | HG04199.hp2 | stop_gained | HIGH | c.1003C>T | p.Gln335* | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1090/2789 | 1003/1086 | 335/361 | chr9 | 26842384 | ||
chr9:26842387
|
G | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1000C>G | p.Gln334Glu | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1087/2789 | 1000/1086 | 334/361 | chr9 | 26842387 | ||
chr9:26842392
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.995C>A | p.Ser332Tyr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1082/2789 | 995/1086 | 332/361 | chr9 | 26842392 | ||
chr9:26842393
|
A | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.994T>A | p.Ser332Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1081/2789 | 994/1086 | 332/361 | chr9 | 26842393 | ||
chr9:26842395
|
G | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.992C>G | p.Pro331Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1079/2789 | 992/1086 | 331/361 | chr9 | 26842395 | ||
chr9:26842396
|
G | A | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.991C>T | p.Pro331Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1078/2789 | 991/1086 | 331/361 | chr9 | 26842396 | ||
chr9:26842398
|
T | G | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.989A>C | p.Gln330Pro | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1076/2789 | 989/1086 | 330/361 | chr9 | 26842398 | ||
chr9:26842399
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.988C>A | p.Gln330Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1075/2789 | 988/1086 | 330/361 | chr9 | 26842399 | ||
chr9:26842405
|
C | A | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.982G>T | p.Asp328Tyr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1069/2789 | 982/1086 | 328/361 | chr9 | 26842405 | ||
chr9:26842408
|
C | G | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.979G>C | p.Glu327Gln | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1066/2789 | 979/1086 | 327/361 | chr9 | 26842408 | ||
chr9:26842413
|
G | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.974C>G | p.Pro325Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1061/2789 | 974/1086 | 325/361 | chr9 | 26842413 | ||
chr9:26842414
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.973C>A | p.Pro325Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1060/2789 | 973/1086 | 325/361 | chr9 | 26842414 | ||
chr9:26842416
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.971C>A | p.Pro324His | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1058/2789 | 971/1086 | 324/361 | chr9 | 26842416 | ||
chr9:26842417
|
G | A | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.970C>T | p.Pro324Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1057/2789 | 970/1086 | 324/361 | chr9 | 26842417 | ||
chr9:26842420
|
C | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.967G>A | p.Val323Ile | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1054/2789 | 967/1086 | 323/361 | chr9 | 26842420 | ||
chr9:26842422
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.965C>A | p.Ala322Asp | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1052/2789 | 965/1086 | 322/361 | chr9 | 26842422 | ||
chr9:26842423
|
C | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.964G>A | p.Ala322Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1051/2789 | 964/1086 | 322/361 | chr9 | 26842423 | ||
chr9:26842428
|
G | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.959C>G | p.Thr320Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1046/2789 | 959/1086 | 320/361 | chr9 | 26842428 | ||
chr9:26842435
|
C | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.952G>A | p.Ala318Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1039/2789 | 952/1086 | 318/361 | chr9 | 26842435 | ||
chr9:26842441
|
G | A | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.946C>T | p.Pro316Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1033/2789 | 946/1086 | 316/361 | chr9 | 26842441 | ||
chr9:26842444
|
C | G | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.943G>C | p.Glu315Gln | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1030/2789 | 943/1086 | 315/361 | chr9 | 26842444 | ||
chr9:26842444
|
C | T | 1 | a0004 | 2 | HG02683.hp1 HG04228.hp1 |
missense_variant | MODERATE | c.943G>A | p.Glu315Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1030/2789 | 943/1086 | 315/361 | chr9 | 26842444 | ||
chr9:26842445
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.942C>A | p.Asn314Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1029/2789 | 942/1086 | 314/361 | chr9 | 26842445 | ||
chr9:26842449
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.938C>A | p.Pro313Gln | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1025/2789 | 938/1086 | 313/361 | chr9 | 26842449 | ||
chr9:26842450
|
G | A | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.937C>T | p.Pro313Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1024/2789 | 937/1086 | 313/361 | chr9 | 26842450 | ||
chr9:26842452
|
C | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.935G>A | p.Ser312Asn | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1022/2789 | 935/1086 | 312/361 | chr9 | 26842452 | ||
chr9:26842456
|
A | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.931T>G | p.Ser311Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1018/2789 | 931/1086 | 311/361 | chr9 | 26842456 | ||
chr9:26842457
|
C | A | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.930G>T | p.Glu310Asp | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1017/2789 | 930/1086 | 310/361 | chr9 | 26842457 | ||
chr9:26842459
|
C | A | 1 | a0006 | 1 | HG04199.hp2 | stop_gained | HIGH | c.928G>T | p.Glu310* | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1015/2789 | 928/1086 | 310/361 | chr9 | 26842459 | ||
chr9:26842465
|
G | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.922C>A | p.Leu308Met | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1009/2789 | 922/1086 | 308/361 | chr9 | 26842465 | ||
chr9:26842467
|
C | A | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.920G>T | p.Gly307Val | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1007/2789 | 920/1086 | 307/361 | chr9 | 26842467 | ||
chr9:26842468
|
C | T | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.919G>A | p.Gly307Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1006/2789 | 919/1086 | 307/361 | chr9 | 26842468 | ||
chr9:26842472
|
A | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.915T>G | p.Ile305Met | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1002/2789 | 915/1086 | 305/361 | chr9 | 26842472 | ||
chr9:26842478
|
A | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.909T>G | p.Asn303Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 996/2789 | 909/1086 | 303/361 | chr9 | 26842478 | ||
chr9:26842479
|
T | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.908A>G | p.Asn303Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 995/2789 | 908/1086 | 303/361 | chr9 | 26842479 | ||
chr9:26842542
|
T | C | 1 | a0003 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.845A>G | p.Asn282Ser | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 932/2789 | 845/1086 | 282/361 | chr9 | 26842542 | ||
chr9:26861108
|
C | T | 2 | a0002a0007 | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
missense_variant | MODERATE | c.697G>A | p.Val233Met | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/6 | 784/2789 | 697/1086 | 233/361 | chr9 | 26861108 | ||
chr9:26886139
|
A | C | 1 | a0007 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.554T>G | p.Leu185Arg | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/6 | 641/2789 | 554/1086 | 185/361 | chr9 | 26886139 | ||
chr9:26892525
|
A | G | 1 | a0005 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.191T>C | p.Val64Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/6 | 278/2789 | 191/1086 | 64/361 | chr9 | 26892525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26842394
|
A | T | 1 | a0006c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.993T>A | p.Pro331Pro | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1080/2789 | 993/1086 | 331/361 | chr9 | 26842394 | ||
chr9:26842415
|
A | C | 1 | a0006c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.972T>G | p.Pro324Pro | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1059/2789 | 972/1086 | 324/361 | chr9 | 26842415 | ||
chr9:26842418
|
A | G | 1 | a0006c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.969T>C | p.Val323Val | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1056/2789 | 969/1086 | 323/361 | chr9 | 26842418 | ||
chr9:26842426
|
G | A | 1 | a0006c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.961C>T | p.Leu321Leu | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1048/2789 | 961/1086 | 321/361 | chr9 | 26842426 | ||
chr9:26842427
|
G | A | 1 | a0006c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.960C>T | p.Thr320Thr | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1047/2789 | 960/1086 | 320/361 | chr9 | 26842427 | ||
chr9:26842436
|
T | C | 1 | a0006c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.951A>G | p.Lys317Lys | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1038/2789 | 951/1086 | 317/361 | chr9 | 26842436 | ||
chr9:26842460
|
T | A | 1 | a0006c0009 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.927A>T | p.Ala309Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1014/2789 | 927/1086 | 309/361 | chr9 | 26842460 | ||
chr9:26842508
|
G | A | 2 | a0002c0003a0007c0006 | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
synonymous_variant | LOW | c.879C>T | p.Asp293Asp | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 966/2789 | 879/1086 | 293/361 | chr9 | 26842508 | ||
chr9:26892656
|
G | A | 2 | a0001c0002a0004c0010 | 111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
synonymous_variant | LOW | c.60C>T | p.Ala20Ala | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/6 | 147/2789 | 60/1086 | 20/361 | chr9 | 26892656 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26841055
|
A | G | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1246T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1246 | chr9 | 26841055 | |||||
chr9:26841143
|
G | A | 1 | a0002c0007t0011 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1158C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1158 | chr9 | 26841143 | |||||
chr9:26841230
|
A | G | 1 | a0005c0005t0009 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 1071 | chr9 | 26841230 | |||||
chr9:26841431
|
T | C | 1 | a0001c0002t0012 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 870 | chr9 | 26841431 | |||||
chr9:26841550
|
G | C | 1 | a0001c0001t0013 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*751C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 751 | chr9 | 26841550 | |||||
chr9:26841704
|
G | A | 1 | a0001c0001t0004 | 2 | HG03041.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*597C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 597 | chr9 | 26841704 | |||||
chr9:26841720
|
A | G | 1 | a0001c0001t0008 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 581 | chr9 | 26841720 | |||||
chr9:26841784
|
G | C | 1 | a0001c0001t0003 | 3 | HG01167.hp1 HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*517C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 517 | chr9 | 26841784 | |||||
chr9:26841798
|
G | A | 2 | a0001c0001t0002a0001c0001t0003 | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*503C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 503 | chr9 | 26841798 | |||||
chr9:26841809
|
G | A | 1 | a0001c0001t0005 | 2 | HG00423.hp2 HG02080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 492 | chr9 | 26841809 | |||||
chr9:26841931
|
A | T | 1 | a0001c0001t0007 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 370 | chr9 | 26841931 | |||||
chr9:26841970
|
G | A | 1 | a0001c0001t0014 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*331C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 331 | chr9 | 26841970 | |||||
chr9:26842046
|
T | C | 1 | a0004c0010t0015 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 255 | chr9 | 26842046 | |||||
chr9:26842151
|
G | C | 1 | a0001c0001t0016 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 6/6 | 150 | chr9 | 26842151 | |||||
chr9:26892789
|
G | A | 1 | a0001c0001t0006 | 2 | HG02559.hp2 HG02717.hp2 |
5_prime_UTR_variant | MODIFIER | c.-74C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/6 | 74 | chr9 | 26892789 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:26842672
|
C | A | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-25G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26842672 | ||||||
chr9:26842794
|
T | C | 7 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-147A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26842794 | ||||||
chr9:26843195
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.740-548C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843195 | ||||||
chr9:26843204
|
C | T | 1 | a0001c0002t0001g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.740-557G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843204 | ||||||
chr9:26843234
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.740-587G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843234 | ||||||
chr9:26843285
|
T | C | 1 | a0003c0004t0001g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.740-638A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843285 | ||||||
chr9:26843290
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.740-643A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843290 | ||||||
chr9:26843344
|
G | A | 14 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(11): Show | 14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.740-697C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843344 | ||||||
chr9:26843431
|
T | C | 3 | a0002c0003t0001g0029a0002c0003t0001g0030a0002c0003t0001g0031 | 3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.740-784A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843431 | ||||||
chr9:26843457
|
G | T | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-810C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843457 | ||||||
chr9:26843486
|
C | A | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-839G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843486 | ||||||
chr9:26843594
|
GT | G | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-948delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843594 | ||||||
chr9:26843598
|
T | TC | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-952_740-951ins others(1): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843598 | ||||||
chr9:26843730
|
G | C | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-1083C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843730 | ||||||
chr9:26843837
|
C | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(121): Show | 132 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.740-1190G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843837 | ||||||
chr9:26843910
|
A | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.740-1263T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26843910 | ||||||
chr9:26844078
|
C | A | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-1431G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844078 | ||||||
chr9:26844133
|
A | G | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-1486T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844133 | ||||||
chr9:26844175
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0156a0001c0001t0001g0175 | 4 | HG01243.hp2 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-1528A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844175 | ||||||
chr9:26844187
|
A | G | 1 | a0001c0002t0001g0276 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.740-1540T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844187 | ||||||
chr9:26844289
|
G | A | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-1642C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844289 | ||||||
chr9:26844318
|
T | C | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-1671A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844318 | ||||||
chr9:26844325
|
C | A | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-1678G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844325 | ||||||
chr9:26844353
|
G | A | 3 | a0002c0003t0001g0029a0002c0003t0001g0030a0002c0003t0001g0031 | 3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.740-1706C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844353 | ||||||
chr9:26844357
|
C | CA | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0099others(9): Show | 12 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.740-1711dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844357 | ||||||
chr9:26844642
|
T | A | 1 | a0001c0002t0001g0303 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.740-1995A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844642 | ||||||
chr9:26844793
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-2146A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844793 | ||||||
chr9:26844844
|
A | C | 1 | a0002c0003t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.740-2197T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844844 | ||||||
chr9:26844845
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(175): Show | 187 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.740-2198G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26844845 | ||||||
chr9:26845128
|
A | T | 18 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(15): Show | 18 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-2481T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845128 | ||||||
chr9:26845206
|
GT | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122 | 3 | HG00733.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.740-2560delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845206 | ||||||
chr9:26845229
|
G | A | 1 | a0001c0002t0001g0301 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.740-2582C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845229 | ||||||
chr9:26845282
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.740-2635C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845282 | ||||||
chr9:26845305
|
C | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(119): Show | 130 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.740-2658G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845305 | ||||||
chr9:26845470
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.740-2823C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845470 | ||||||
chr9:26845485
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.740-2838G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845485 | ||||||
chr9:26845601
|
C | T | 7 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-2954G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845601 | ||||||
chr9:26845602
|
C | G | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-2955G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845602 | ||||||
chr9:26845618
|
C | T | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-2971G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845618 | ||||||
chr9:26845734
|
G | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-3087C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845734 | ||||||
chr9:26845841
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG00140.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.740-3194G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845841 | ||||||
chr9:26845849
|
G | A | 3 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0032 | 3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-3202C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845849 | ||||||
chr9:26845980
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-3333C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845980 | ||||||
chr9:26845980
|
G | GT | 23 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-3334dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26845980 | ||||||
chr9:26846074
|
T | C | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-3427A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846074 | ||||||
chr9:26846107
|
T | A | 1 | a0005c0005t0009g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.740-3460A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846107 | ||||||
chr9:26846113
|
A | AC | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-3467dupG | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846113 | ||||||
chr9:26846116
|
C | G | 1 | a0005c0005t0009g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.740-3469G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846116 | ||||||
chr9:26846184
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.740-3537G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846184 | ||||||
chr9:26846185
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(177): Show | 189 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.740-3538T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846185 | ||||||
chr9:26846247
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-3600G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846247 | ||||||
chr9:26846355
|
G | T | 1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.740-3708C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846355 | ||||||
chr9:26846403
|
G | A | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-3756C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846403 | ||||||
chr9:26846415
|
C | CA | 23 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(20): Show | 23 | HG00642.hp2 HG00735.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-3769dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | ||||||
chr9:26846415
|
C | CAA | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0066others(68): Show | 75 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.740-3770_740-3769d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | ||||||
chr9:26846415
|
C | CAAA | 39 | a0001c0001t0001g0037a0001c0001t0001g0071a0001c0001t0001g0082others(36): Show | 43 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.740-3771_740-3769d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | ||||||
chr9:26846415
|
C | CAAAA | 6 | a0001c0002t0001g0257a0001c0002t0001g0284a0001c0002t0001g0285others(3): Show | 6 | HG00621.hp2 HG02027.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-3772_740-3769d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | ||||||
chr9:26846415
|
CA | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(27): Show | 35 | HG00609.hp2 HG00733.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.740-3769delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | ||||||
chr9:26846415
|
CAAAAAAA others(4): Show |
C | 22 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0134others(19): Show | 23 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-3779_740-3769d others(13): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | ||||||
chr9:26846415
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0001g0307 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.740-3781_740-3769d others(15): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846415 | ||||||
chr9:26846437
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18747.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.740-3790T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846437 | ||||||
chr9:26846438
|
A | AG | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.740-3792_740-3791i others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846438 | ||||||
chr9:26846438
|
A | G | 2 | a0002c0003t0001g0020a0002c0003t0001g0021 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.740-3791T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846438 | ||||||
chr9:26846439
|
AG | A | 13 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(10): Show | 13 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.740-3793delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846439 | ||||||
chr9:26846440
|
G | A | 13 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(10): Show | 13 | HG00733.hp1 HG01891.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.740-3793C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846440 | ||||||
chr9:26846441
|
A | AG | 3 | a0002c0003t0001g0024a0002c0003t0001g0033a0002c0003t0001g0036 | 3 | HG02257.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.740-3795_740-3794i others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846441 | ||||||
chr9:26846441
|
A | G | 3 | a0002c0003t0001g0034a0002c0003t0001g0035a0002c0007t0011g0026 | 3 | HG01891.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.740-3794T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846441 | ||||||
chr9:26846442
|
AG | A | 11 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(8): Show | 12 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.740-3796delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846442 | ||||||
chr9:26846443
|
G | A | 3 | a0002c0003t0001g0024a0002c0003t0001g0033a0002c0003t0001g0036 | 3 | HG02257.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.740-3796C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846443 | ||||||
chr9:26846443
|
G | GAA | 3 | a0002c0003t0001g0034a0002c0003t0001g0035a0002c0007t0011g0026 | 3 | HG01891.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.740-3798_740-3797d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846443 | ||||||
chr9:26846448
|
A | G | 3 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0032 | 3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-3801T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846448 | ||||||
chr9:26846453
|
A | G | 3 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0032 | 3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.740-3806T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846453 | ||||||
chr9:26846751
|
G | A | 3 | a0001c0002t0001g0351a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG02451.hp1 NA19030.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.740-4104C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846751 | ||||||
chr9:26846782
|
G | A | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-4135C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846782 | ||||||
chr9:26846810
|
C | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02615.hp2 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-4163G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846810 | ||||||
chr9:26846862
|
T | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-4215A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846862 | ||||||
chr9:26846928
|
C | G | 7 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-4281G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26846928 | ||||||
chr9:26847021
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.740-4374C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847021 | ||||||
chr9:26847117
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.740-4470A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847117 | ||||||
chr9:26847135
|
A | G | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.740-4488T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847135 | ||||||
chr9:26847198
|
A | AT | 13 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(10): Show | 13 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.740-4552dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTT | 18 | a0001c0001t0001g0041a0001c0001t0001g0093a0001c0001t0001g0153others(15): Show | 18 | HG00140.hp1 HG00738.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.740-4554_740-4552d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTT | 29 | a0001c0001t0001g0136a0001c0001t0001g0156a0001c0001t0001g0157others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.740-4555_740-4552d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTT | 21 | a0001c0001t0001g0004a0001c0001t0001g0134a0001c0001t0001g0147others(18): Show | 23 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-4556_740-4552d others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTT | 11 | a0001c0001t0001g0009a0001c0001t0001g0133a0001c0001t0001g0138others(8): Show | 12 | HG01123.hp2 HG01515.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.740-4557_740-4552d others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0179 | 2 | HG00735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.740-4561_740-4552d others(12): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0079a0001c0001t0001g0146a0001c0001t0001g0178others(1): Show | 4 | HG01258.hp1 HG03130.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-4562_740-4552d others(13): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0193 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.740-4563_740-4552d others(14): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0192 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.740-4564_740-4552d others(15): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.740-4565_740-4552d others(16): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0092 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.740-4566_740-4552d others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0177a0001c0001t0001g0221 | 2 | HG01975.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.740-4567_740-4552d others(18): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0094 | 2 | HG00408.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.740-4570_740-4552d others(21): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0095 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.740-4573_740-4552d others(24): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
A | T | 1 | a0001c0001t0002g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.740-4551T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTT | A | 11 | a0001c0001t0001g0107a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG00609.hp1 HG01099.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-4554_740-4552d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTT | A | 45 | a0001c0001t0001g0070a0001c0001t0001g0082a0001c0001t0001g0086others(42): Show | 46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.740-4555_740-4552d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTT | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(81): Show | 91 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.740-4556_740-4552d others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTT | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0101others(12): Show | 15 | HG00323.hp1 HG01109.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.740-4557_740-4552d others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0158a0001c0001t0001g0164others(5): Show | 9 | HG00733.hp2 HG01981.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-4558_740-4552d others(9): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT others(1): Show |
A | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(30): Show | 37 | HG00423.hp1 HG00609.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.740-4559_740-4552d others(10): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0132a0002c0007t0011g0026 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.740-4561_740-4552d others(12): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0150a0001c0001t0002g0227 | 2 | HG01123.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.740-4562_740-4552d others(13): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.740-4563_740-4552d others(14): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0090 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.740-4565_740-4552d others(16): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0001g0046a0001c0001t0001g0073 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.740-4567_740-4552d others(18): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847198
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0002t0001g0340 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.740-4571_740-4552d others(22): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847198 | ||||||
chr9:26847235
|
C | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-4588G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847235 | ||||||
chr9:26847238
|
G | A | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.740-4591C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847238 | ||||||
chr9:26847304
|
T | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0066others(10): Show | 14 | HG00438.hp1 HG00673.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.740-4657A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847304 | ||||||
chr9:26847444
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.740-4797C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847444 | ||||||
chr9:26847461
|
G | A | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-4814C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847461 | ||||||
chr9:26847503
|
C | T | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.740-4856G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847503 | ||||||
chr9:26847509
|
C | T | 10 | a0001c0001t0002g0246a0002c0003t0001g0001a0002c0003t0001g0018others(7): Show | 11 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-4862G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847509 | ||||||
chr9:26847512
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0008g0206 | 2 | NA18975.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.740-4865G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847512 | ||||||
chr9:26847530
|
T | A | 5 | a0001c0001t0002g0236a0001c0001t0002g0240a0001c0001t0002g0245others(2): Show | 5 | HG00642.hp1 HG01069.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-4883A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847530 | ||||||
chr9:26847545
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.740-4898A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847545 | ||||||
chr9:26847649
|
G | A | 2 | a0004c0008t0001g0089a0004c0010t0015g0331 | 2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.740-5002C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847649 | ||||||
chr9:26847717
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(28): Show | 33 | HG00408.hp1 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.740-5070A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847717 | ||||||
chr9:26847729
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.740-5082A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847729 | ||||||
chr9:26847757
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.740-5110G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847757 | ||||||
chr9:26847979
|
T | C | 23 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.740-5332A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26847979 | ||||||
chr9:26848007
|
T | C | 1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.740-5360A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848007 | ||||||
chr9:26848071
|
A | C | 1 | a0001c0001t0001g0172 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.740-5424T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848071 | ||||||
chr9:26848108
|
T | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-5461A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848108 | ||||||
chr9:26848115
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5468A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848115 | ||||||
chr9:26848357
|
A | C | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5710T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848357 | ||||||
chr9:26848358
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5711G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848358 | ||||||
chr9:26848409
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(173): Show | 185 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.740-5762T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848409 | ||||||
chr9:26848440
|
C | T | 1 | a0001c0002t0001g0300 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.740-5793G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848440 | ||||||
chr9:26848446
|
G | C | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5799C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848446 | ||||||
chr9:26848470
|
T | G | 1 | a0001c0002t0001g0282 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.740-5823A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848470 | ||||||
chr9:26848515
|
C | CA | 10 | a0001c0001t0001g0109a0001c0002t0001g0272a0001c0002t0001g0273others(7): Show | 11 | HG01192.hp2 HG02027.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.740-5869dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848515 | ||||||
chr9:26848523
|
G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(176): Show | 188 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.740-5876C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848523 | ||||||
chr9:26848568
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5921T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848568 | ||||||
chr9:26848569
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-5922A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848569 | ||||||
chr9:26848632
|
A | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-5985T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848632 | ||||||
chr9:26848647
|
C | T | 1 | a0001c0002t0001g0324 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.740-6000G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848647 | ||||||
chr9:26848652
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6005A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848652 | ||||||
chr9:26848711
|
T | C | 3 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019 | 4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-6064A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848711 | ||||||
chr9:26848838
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6191T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848838 | ||||||
chr9:26848839
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6192A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848839 | ||||||
chr9:26848907
|
T | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(113): Show | 124 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.740-6260A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848907 | ||||||
chr9:26848928
|
A | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0214 | 3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.740-6281T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848928 | ||||||
chr9:26848944
|
T | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.740-6297A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26848944 | ||||||
chr9:26849116
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.740-6469A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849116 | ||||||
chr9:26849372
|
C | T | 1 | a0001c0002t0001g0260 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.740-6725G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849372 | ||||||
chr9:26849415
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.740-6768A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849415 | ||||||
chr9:26849442
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6795T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849442 | ||||||
chr9:26849446
|
T | C | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-6799A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849446 | ||||||
chr9:26849498
|
T | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02615.hp2 HG02683.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-6851A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849498 | ||||||
chr9:26849572
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.740-6925A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849572 | ||||||
chr9:26849597
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-6950G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849597 | ||||||
chr9:26849608
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.740-6961T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849608 | ||||||
chr9:26849619
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.740-6972A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849619 | ||||||
chr9:26849684
|
CCTTTTTT others(1): Show |
C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-7045_740-7038d others(10): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849684 | ||||||
chr9:26849744
|
G | A | 10 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(7): Show | 10 | HG00597.hp2 HG02135.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-7097C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849744 | ||||||
chr9:26849812
|
G | C | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.740-7165C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849812 | ||||||
chr9:26849841
|
A | AT | 6 | a0001c0001t0001g0154a0001c0001t0004g0080a0001c0001t0004g0081others(3): Show | 6 | HG01978.hp1 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-7195dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849841 | ||||||
chr9:26849841
|
AT | A | 9 | a0001c0001t0001g0156a0001c0002t0001g0258a0001c0002t0001g0292others(6): Show | 9 | HG00438.hp1 HG00673.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.740-7195delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849841 | ||||||
chr9:26849950
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-7303A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849950 | ||||||
chr9:26849963
|
C | T | 2 | a0001c0001t0001g0138a0001c0002t0001g0322 | 2 | HG00597.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.740-7316G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26849963 | ||||||
chr9:26850039
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.740-7392G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850039 | ||||||
chr9:26850058
|
TTGATCTG others(8): Show |
T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-7426_740-7412d others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850058 | ||||||
chr9:26850144
|
A | C | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-7497T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850144 | ||||||
chr9:26850196
|
G | T | 4 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-7549C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850196 | ||||||
chr9:26850208
|
C | T | 2 | a0002c0003t0001g0027a0002c0003t0001g0028 | 2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.740-7561G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850208 | ||||||
chr9:26850316
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.740-7669G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850316 | ||||||
chr9:26850495
|
G | A | 14 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(11): Show | 14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.740-7848C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850495 | ||||||
chr9:26850595
|
C | T | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.740-7948G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850595 | ||||||
chr9:26850611
|
C | T | 45 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(42): Show | 46 | HG00733.hp1 HG01192.hp2 HG01256.hp2 others(43): Show |
intron_variant | MODIFIER | c.740-7964G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850611 | ||||||
chr9:26850719
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 7 | HG01515.hp2 HG01517.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.740-8072A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850719 | ||||||
chr9:26850768
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.740-8121T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850768 | ||||||
chr9:26850994
|
G | A | 2 | a0001c0002t0001g0011a0001c0002t0001g0257 | 3 | HG02015.hp2 NA18945.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.740-8347C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26850994 | ||||||
chr9:26851098
|
T | TAGAAGTA others(343): Show |
1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.740-8452_740-8451i others(352): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851098 | ||||||
chr9:26851197
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(115): Show | 126 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.740-8550G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851197 | ||||||
chr9:26851223
|
A | C | 6 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(3): Show | 6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-8576T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851223 | ||||||
chr9:26851265
|
A | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-8618T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851265 | ||||||
chr9:26851342
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(123): Show | 134 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.740-8695A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851342 | ||||||
chr9:26851343
|
G | A | 2 | a0001c0002t0001g0341a0001c0002t0001g0342 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.740-8696C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851343 | ||||||
chr9:26851347
|
G | A | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.740-8700C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851347 | ||||||
chr9:26851403
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.740-8756C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851403 | ||||||
chr9:26851411
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-8764G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851411 | ||||||
chr9:26851482
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(115): Show | 126 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.740-8835G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851482 | ||||||
chr9:26851483
|
C | T | 9 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0015others(6): Show | 12 | HG00639.hp1 HG01081.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.740-8836G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851483 | ||||||
chr9:26851516
|
T | C | 2 | a0001c0002t0001g0347a0001c0002t0001g0348 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.740-8869A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851516 | ||||||
chr9:26851931
|
A | G | 1 | a0001c0002t0001g0282 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.739+9135T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851931 | ||||||
chr9:26851937
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.739+9129A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851937 | ||||||
chr9:26851943
|
A | G | 1 | a0001c0002t0001g0285 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.739+9123T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851943 | ||||||
chr9:26851951
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0066others(83): Show | 92 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.739+9115A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26851951 | ||||||
chr9:26852028
|
A | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(119): Show | 130 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.739+9038T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852028 | ||||||
chr9:26852062
|
A | T | 14 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(11): Show | 14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.739+9004T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852062 | ||||||
chr9:26852152
|
T | TG | 355 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(352): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.739+8913dupC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852152 | ||||||
chr9:26852282
|
C | T | 1 | a0002c0003t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.739+8784G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852282 | ||||||
chr9:26852327
|
C | T | 2 | a0004c0008t0001g0089a0004c0010t0015g0331 | 2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.739+8739G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852327 | ||||||
chr9:26852386
|
C | T | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.739+8680G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852386 | ||||||
chr9:26852387
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.739+8679C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852387 | ||||||
chr9:26852470
|
A | C | 1 | a0004c0008t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.739+8596T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852470 | ||||||
chr9:26852534
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.739+8532A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852534 | ||||||
chr9:26852543
|
G | C | 1 | a0001c0002t0001g0323 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.739+8523C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852543 | ||||||
chr9:26852605
|
T | C | 1 | a0004c0010t0015g0331 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.739+8461A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852605 | ||||||
chr9:26852631
|
C | G | 1 | a0001c0002t0001g0256 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.739+8435G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852631 | ||||||
chr9:26852772
|
G | C | 8 | a0001c0001t0002g0126a0001c0001t0002g0223a0001c0001t0002g0226others(5): Show | 8 | HG01123.hp1 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+8294C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26852772 | ||||||
chr9:26853203
|
T | C | 6 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(3): Show | 6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+7863A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853203 | ||||||
chr9:26853285
|
T | C | 1 | a0001c0002t0001g0256 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.739+7781A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853285 | ||||||
chr9:26853286
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+7780C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853286 | ||||||
chr9:26853421
|
T | A | 2 | a0002c0007t0011g0026a0007c0006t0001g0025 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.739+7645A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853421 | ||||||
chr9:26853487
|
A | G | 1 | a0002c0003t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.739+7579T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853487 | ||||||
chr9:26853781
|
A | T | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.739+7285T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853781 | ||||||
chr9:26853824
|
C | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+7242G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853824 | ||||||
chr9:26853847
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0106 | 3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.739+7219A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853847 | ||||||
chr9:26853895
|
A | G | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+7171T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26853895 | ||||||
chr9:26854073
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.739+6993A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854073 | ||||||
chr9:26854132
|
G | GA | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+6933dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854132 | ||||||
chr9:26854194
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.739+6872G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854194 | ||||||
chr9:26854449
|
A | G | 1 | a0001c0002t0001g0262 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.739+6617T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854449 | ||||||
chr9:26854482
|
G | GCTGAATG others(3): Show |
20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+6574_739+6583d others(12): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854482 | ||||||
chr9:26854535
|
C | T | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.739+6531G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854535 | ||||||
chr9:26854740
|
G | T | 8 | a0001c0001t0002g0126a0001c0001t0002g0223a0001c0001t0002g0226others(5): Show | 8 | HG01123.hp1 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+6326C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854740 | ||||||
chr9:26854802
|
A | G | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+6264T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854802 | ||||||
chr9:26854825
|
G | A | 7 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.739+6241C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854825 | ||||||
chr9:26854990
|
A | C | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+6076T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26854990 | ||||||
chr9:26855058
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.739+6008A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855058 | ||||||
chr9:26855078
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.739+5988A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855078 | ||||||
chr9:26855103
|
G | C | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+5963C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855103 | ||||||
chr9:26855128
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.739+5938A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855128 | ||||||
chr9:26855316
|
G | A | 1 | a0003c0004t0001g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.739+5750C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855316 | ||||||
chr9:26855322
|
G | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+5744C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855322 | ||||||
chr9:26855323
|
G | C | 1 | a0001c0001t0001g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.739+5743C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855323 | ||||||
chr9:26855635
|
C | T | 1 | a0001c0002t0001g0316 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.739+5431G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26855635 | ||||||
chr9:26856013
|
T | G | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.739+5053A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856013 | ||||||
chr9:26856128
|
A | AG | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(136): Show | 147 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.739+4937dupC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856128 | ||||||
chr9:26856131
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.739+4935C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856131 | ||||||
chr9:26856131
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.739+4935C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856131 | ||||||
chr9:26856133
|
G | GA | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+4932_739+4933i others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856133 | ||||||
chr9:26856218
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.739+4848G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856218 | ||||||
chr9:26856279
|
T | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+4787A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856279 | ||||||
chr9:26856421
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG00140.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.739+4645T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856421 | ||||||
chr9:26856441
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.739+4625C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856441 | ||||||
chr9:26856707
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.739+4359A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856707 | ||||||
chr9:26856754
|
A | C | 23 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.739+4312T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856754 | ||||||
chr9:26856866
|
A | G | 1 | a0001c0002t0001g0349 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.739+4200T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856866 | ||||||
chr9:26856986
|
T | C | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+4080A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856986 | ||||||
chr9:26856990
|
G | A | 1 | a0001c0001t0010g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.739+4076C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26856990 | ||||||
chr9:26857047
|
G | C | 1 | a0001c0001t0001g0005 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.739+4019C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857047 | ||||||
chr9:26857089
|
GT | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3976delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857089 | ||||||
chr9:26857232
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0014g0187 | 3 | NA18944.hp2 NA18970.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.739+3834G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857232 | ||||||
chr9:26857246
|
C | T | 313 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(310): Show | 328 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.739+3820G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857246 | ||||||
chr9:26857316
|
C | G | 23 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.739+3750G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857316 | ||||||
chr9:26857351
|
G | A | 9 | a0001c0002t0001g0285a0001c0002t0001g0286a0001c0002t0001g0287others(6): Show | 9 | HG00621.hp2 NA18959.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3715C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857351 | ||||||
chr9:26857359
|
T | C | 60 | a0001c0001t0001g0136a0001c0001t0001g0241a0001c0001t0002g0010others(57): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.739+3707A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857359 | ||||||
chr9:26857543
|
A | C | 1 | a0001c0002t0001g0273 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.739+3523T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857543 | ||||||
chr9:26857564
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3502C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857564 | ||||||
chr9:26857582
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.739+3484T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857582 | ||||||
chr9:26857877
|
C | CA | 130 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(127): Show | 138 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.739+3188dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857877 | ||||||
chr9:26857899
|
T | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+3167A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857899 | ||||||
chr9:26857960
|
A | G | 14 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(11): Show | 14 | HG01256.hp2 HG02056.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.739+3106T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26857960 | ||||||
chr9:26858226
|
AGAGATAT others(8): Show |
A | 21 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(18): Show | 21 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.739+2825_739+2839d others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858226 | ||||||
chr9:26858243
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.739+2823G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858243 | ||||||
chr9:26858353
|
T | C | 1 | a0001c0002t0001g0267 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.739+2713A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858353 | ||||||
chr9:26858447
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+2619G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858447 | ||||||
chr9:26858524
|
A | T | 1 | a0002c0003t0001g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.739+2542T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858524 | ||||||
chr9:26858531
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+2535C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858531 | ||||||
chr9:26858557
|
T | C | 9 | a0001c0002t0001g0285a0001c0002t0001g0286a0001c0002t0001g0287others(6): Show | 9 | HG00621.hp2 NA18959.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.739+2509A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858557 | ||||||
chr9:26858561
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+2505C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858561 | ||||||
chr9:26858608
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.739+2458C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858608 | ||||||
chr9:26858632
|
T | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(171): Show | 182 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.739+2434A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858632 | ||||||
chr9:26858679
|
C | T | 1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.739+2387G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858679 | ||||||
chr9:26858738
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0149a0001c0001t0001g0150 | 4 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+2328C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858738 | ||||||
chr9:26858813
|
G | A | 174 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(171): Show | 182 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.739+2253C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858813 | ||||||
chr9:26858822
|
C | CAA | 20 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0109others(17): Show | 20 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.739+2242_739+2243d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858822 | ||||||
chr9:26858822
|
CA | C | 15 | a0001c0001t0001g0136a0001c0001t0001g0215a0001c0001t0002g0203others(12): Show | 16 | HG01192.hp2 HG01255.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.739+2243delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858822 | ||||||
chr9:26858833
|
A | G | 2 | a0003c0004t0001g0252a0003c0004t0001g0253 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+2233T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858833 | ||||||
chr9:26858954
|
C | T | 75 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(72): Show | 80 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.739+2112G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858954 | ||||||
chr9:26858978
|
T | C | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+2088A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858978 | ||||||
chr9:26858984
|
G | C | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+2082C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858984 | ||||||
chr9:26858996
|
C | CA | 152 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0051others(149): Show | 161 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.739+2069dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858996 | ||||||
chr9:26858996
|
C | CAA | 6 | a0001c0001t0001g0053a0001c0001t0001g0110a0001c0002t0001g0269others(3): Show | 6 | HG00621.hp1 HG03098.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+2068_739+2069d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858996 | ||||||
chr9:26858996
|
CA | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0094others(7): Show | 10 | HG00408.hp2 HG01070.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.739+2069delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26858996 | ||||||
chr9:26859142
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.739+1924C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859142 | ||||||
chr9:26859145
|
C | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.739+1921G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859145 | ||||||
chr9:26859352
|
CTGAG | C | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0146others(5): Show | 8 | HG01123.hp2 HG01192.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.739+1710_739+1713d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859352 | ||||||
chr9:26859373
|
C | A | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.739+1693G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859373 | ||||||
chr9:26859476
|
C | T | 1 | a0001c0002t0001g0337 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.739+1590G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859476 | ||||||
chr9:26859503
|
G | C | 1 | a0001c0002t0001g0329 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.739+1563C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859503 | ||||||
chr9:26859509
|
G | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+1557C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859509 | ||||||
chr9:26859642
|
T | C | 3 | a0002c0003t0001g0029a0002c0003t0001g0030a0002c0003t0001g0031 | 3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.739+1424A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859642 | ||||||
chr9:26859664
|
T | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.739+1402A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859664 | ||||||
chr9:26859722
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.739+1344T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26859722 | ||||||
chr9:26860123
|
A | G | 1 | a0005c0005t0009g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.739+943T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860123 | ||||||
chr9:26860125
|
A | C | 1 | a0005c0005t0009g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.739+941T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860125 | ||||||
chr9:26860230
|
A | G | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+836T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860230 | ||||||
chr9:26860357
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.739+709A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860357 | ||||||
chr9:26860360
|
T | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(170): Show | 181 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.739+706A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860360 | ||||||
chr9:26860361
|
G | A | 4 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0296others(1): Show | 4 | HG00438.hp1 HG00673.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+705C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860361 | ||||||
chr9:26860558
|
C | T | 1 | a0001c0002t0001g0305 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.739+508G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860558 | ||||||
chr9:26860568
|
G | A | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+498C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860568 | ||||||
chr9:26860578
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.739+488C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860578 | ||||||
chr9:26860611
|
T | C | 1 | a0001c0002t0001g0321 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.739+455A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860611 | ||||||
chr9:26860652
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.739+414G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860652 | ||||||
chr9:26860706
|
G | A | 2 | a0001c0002t0001g0278a0001c0002t0001g0294 | 2 | NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.739+360C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860706 | ||||||
chr9:26860713
|
A | AC | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+352dupG | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860713 | ||||||
chr9:26860715
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0194a0001c0001t0001g0198 | 3 | NA18612.hp1 NA18982.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.739+351G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860715 | ||||||
chr9:26860723
|
T | G | 47 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(44): Show | 48 | HG00733.hp1 HG01192.hp2 HG01256.hp2 others(45): Show |
intron_variant | MODIFIER | c.739+343A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860723 | ||||||
chr9:26860733
|
G | C | 2 | a0002c0003t0001g0001a0002c0003t0001g0019 | 3 | HG01192.hp2 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.739+333C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860733 | ||||||
chr9:26860740
|
A | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+326T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860740 | ||||||
chr9:26860748
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+318C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860748 | ||||||
chr9:26860780
|
G | C | 1 | a0004c0008t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.739+286C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860780 | ||||||
chr9:26860891
|
A | G | 1 | a0001c0002t0001g0323 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.739+175T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26860891 | ||||||
chr9:26861032
|
A | C | 4 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+34T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 5/5 | chr9 | 26861032 | ||||||
chr9:26861154
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.666-15A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861154 | ||||||
chr9:26861300
|
A | G | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-161T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861300 | ||||||
chr9:26861435
|
T | C | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-296A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861435 | ||||||
chr9:26861605
|
G | A | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-466C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861605 | ||||||
chr9:26861675
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.666-536C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861675 | ||||||
chr9:26861757
|
T | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA19077.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.666-618A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26861757 | ||||||
chr9:26862002
|
G | GTT | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-864_666-863ins others(2): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862002 | ||||||
chr9:26862021
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-882G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862021 | ||||||
chr9:26862170
|
C | T | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-1031G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862170 | ||||||
chr9:26862350
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.666-1211G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862350 | ||||||
chr9:26862379
|
T | C | 23 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 23 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.666-1240A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862379 | ||||||
chr9:26862415
|
C | CA | 27 | a0001c0001t0001g0061a0001c0001t0001g0216a0001c0001t0001g0219others(24): Show | 28 | HG00408.hp1 HG01192.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-1277dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862415 | ||||||
chr9:26862518
|
T | C | 2 | a0002c0003t0001g0027a0002c0003t0001g0028 | 2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.666-1379A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862518 | ||||||
chr9:26862704
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0156a0001c0001t0001g0175others(3): Show | 7 | HG01243.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-1565C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862704 | ||||||
chr9:26862806
|
C | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-1667G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862806 | ||||||
chr9:26862961
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01516.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.666-1822C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26862961 | ||||||
chr9:26863119
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-1980G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863119 | ||||||
chr9:26863181
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.666-2042A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863181 | ||||||
chr9:26863245
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(111): Show | 121 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.666-2106G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863245 | ||||||
chr9:26863249
|
A | G | 1 | a0001c0002t0001g0284 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.666-2110T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863249 | ||||||
chr9:26863356
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.666-2217C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863356 | ||||||
chr9:26863532
|
C | T | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-2393G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863532 | ||||||
chr9:26863671
|
C | A | 2 | a0001c0002t0001g0343a0001c0002t0001g0346 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.666-2532G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863671 | ||||||
chr9:26863772
|
T | TA | 14 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0076others(11): Show | 14 | HG00558.hp2 HG00741.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.666-2634dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863772 | ||||||
chr9:26863772
|
TA | T | 147 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.666-2634delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863772 | ||||||
chr9:26863772
|
TAA | T | 26 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(23): Show | 27 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.666-2635_666-2634d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863772 | ||||||
chr9:26863773
|
A | T | 2 | a0002c0003t0001g0020a0002c0003t0001g0023 | 2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.666-2634T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863773 | ||||||
chr9:26863774
|
A | T | 5 | a0002c0003t0001g0018a0002c0003t0001g0021a0002c0003t0001g0022others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-2635T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863774 | ||||||
chr9:26863775
|
A | T | 11 | a0002c0003t0001g0001a0002c0003t0001g0019a0002c0003t0001g0024others(8): Show | 12 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.666-2636T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863775 | ||||||
chr9:26863896
|
A | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-2757T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863896 | ||||||
chr9:26863978
|
T | C | 7 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-2839A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863978 | ||||||
chr9:26863997
|
A | C | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-2858T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26863997 | ||||||
chr9:26864041
|
G | C | 9 | a0001c0002t0001g0285a0001c0002t0001g0286a0001c0002t0001g0287others(6): Show | 9 | HG00621.hp2 NA18959.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-2902C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864041 | ||||||
chr9:26864121
|
A | C | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-2982T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864121 | ||||||
chr9:26864251
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3112A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864251 | ||||||
chr9:26864490
|
A | AC | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3352dupG | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864490 | ||||||
chr9:26864530
|
C | T | 3 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0032 | 3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.666-3391G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864530 | ||||||
chr9:26864565
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3426A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864565 | ||||||
chr9:26864566
|
G | A | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-3427C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864566 | ||||||
chr9:26864604
|
C | A | 3 | a0002c0003t0001g0029a0002c0003t0001g0030a0002c0003t0001g0031 | 3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.666-3465G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864604 | ||||||
chr9:26864614
|
C | T | 1 | a0004c0008t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.666-3475G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864614 | ||||||
chr9:26864681
|
G | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(121): Show | 132 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.666-3542C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864681 | ||||||
chr9:26864709
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3570A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864709 | ||||||
chr9:26864726
|
A | G | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-3587T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864726 | ||||||
chr9:26864731
|
A | G | 4 | a0001c0001t0001g0166a0001c0001t0001g0195a0001c0001t0001g0197others(1): Show | 4 | HG02129.hp2 HG02132.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-3592T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864731 | ||||||
chr9:26864780
|
G | T | 35 | a0001c0001t0002g0010a0001c0001t0002g0126a0001c0001t0002g0204others(32): Show | 36 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.666-3641C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864780 | ||||||
chr9:26864835
|
C | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3696G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864835 | ||||||
chr9:26864856
|
C | T | 1 | a0001c0002t0001g0299 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.666-3717G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864856 | ||||||
chr9:26864930
|
G | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-3791C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26864930 | ||||||
chr9:26865003
|
C | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-3864G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865003 | ||||||
chr9:26865040
|
T | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-3901A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865040 | ||||||
chr9:26865049
|
T | A | 1 | a0001c0002t0001g0303 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.666-3910A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865049 | ||||||
chr9:26865449
|
G | A | 21 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(18): Show | 21 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.666-4310C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865449 | ||||||
chr9:26865460
|
GT | G | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4322delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865460 | ||||||
chr9:26865481
|
G | T | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4342C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865481 | ||||||
chr9:26865501
|
G | T | 1 | a0001c0001t0002g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.666-4362C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865501 | ||||||
chr9:26865516
|
CTA | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4379_666-4378d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865516 | ||||||
chr9:26865524
|
C | CA | 15 | a0001c0001t0001g0075a0001c0001t0001g0099a0001c0001t0001g0100others(12): Show | 15 | HG00323.hp1 HG01074.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.666-4386dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865524 | ||||||
chr9:26865524
|
CA | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(117): Show | 127 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.666-4386delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865524 | ||||||
chr9:26865538
|
A | T | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-4399T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865538 | ||||||
chr9:26865579
|
AG | A | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4441delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865579 | ||||||
chr9:26865698
|
A | G | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4559T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865698 | ||||||
chr9:26865820
|
G | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4681C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865820 | ||||||
chr9:26865891
|
A | T | 38 | a0001c0001t0002g0010a0001c0001t0002g0124a0001c0001t0002g0125others(35): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.666-4752T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865891 | ||||||
chr9:26865897
|
A | G | 1 | a0003c0004t0001g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.666-4758T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865897 | ||||||
chr9:26865904
|
T | C | 5 | a0001c0001t0004g0080a0001c0001t0004g0081a0003c0004t0001g0097others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-4765A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865904 | ||||||
chr9:26865990
|
A | G | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4851T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26865990 | ||||||
chr9:26866001
|
T | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4862A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866001 | ||||||
chr9:26866003
|
T | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4864A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866003 | ||||||
chr9:26866008
|
G | A | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4869C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866008 | ||||||
chr9:26866018
|
T | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4879A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866018 | ||||||
chr9:26866135
|
CCA | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-4998_666-4997d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866135 | ||||||
chr9:26866168
|
A | G | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-5029T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866168 | ||||||
chr9:26866171
|
C | T | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-5032G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866171 | ||||||
chr9:26866222
|
C | T | 1 | a0001c0002t0001g0273 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.666-5083G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866222 | ||||||
chr9:26866232
|
T | A | 174 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(171): Show | 182 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.666-5093A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866232 | ||||||
chr9:26866264
|
T | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-5125A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866264 | ||||||
chr9:26866331
|
T | C | 1 | a0001c0002t0001g0296 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.666-5192A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866331 | ||||||
chr9:26866486
|
T | G | 1 | a0002c0003t0001g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.666-5347A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866486 | ||||||
chr9:26866644
|
T | C | 25 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(22): Show | 25 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.666-5505A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866644 | ||||||
chr9:26866648
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.666-5509T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866648 | ||||||
chr9:26866736
|
A | T | 1 | a0001c0001t0001g0006 | 2 | HG01081.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.666-5597T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866736 | ||||||
chr9:26866778
|
T | C | 1 | a0001c0002t0001g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.666-5639A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866778 | ||||||
chr9:26866912
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.666-5773G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866912 | ||||||
chr9:26866913
|
G | T | 5 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0114others(2): Show | 5 | HG01256.hp2 HG02735.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-5774C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866913 | ||||||
chr9:26866925
|
G | T | 10 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(7): Show | 10 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-5786C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26866925 | ||||||
chr9:26867088
|
T | C | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.666-5949A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867088 | ||||||
chr9:26867123
|
G | A | 1 | a0004c0008t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.666-5984C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867123 | ||||||
chr9:26867129
|
G | C | 1 | a0001c0002t0001g0289 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.666-5990C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867129 | ||||||
chr9:26867211
|
C | G | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6072G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867211 | ||||||
chr9:26867213
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0122others(1): Show | 4 | HG00733.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-6074A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867213 | ||||||
chr9:26867335
|
C | T | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6196G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867335 | ||||||
chr9:26867496
|
C | G | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6357G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867496 | ||||||
chr9:26867565
|
A | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6426T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867565 | ||||||
chr9:26867682
|
A | G | 1 | a0001c0002t0001g0349 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666-6543T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867682 | ||||||
chr9:26867708
|
T | C | 11 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0024others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-6569A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867708 | ||||||
chr9:26867740
|
G | C | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-6601C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867740 | ||||||
chr9:26867768
|
T | C | 1 | a0001c0002t0001g0303 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.666-6629A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867768 | ||||||
chr9:26867773
|
T | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | NA18964.hp1 NA18967.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-6634A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867773 | ||||||
chr9:26867839
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.666-6700A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26867839 | ||||||
chr9:26868024
|
TA | T | 7 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-6886delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868024 | ||||||
chr9:26868087
|
T | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-6948A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868087 | ||||||
chr9:26868211
|
C | T | 173 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(170): Show | 181 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.666-7072G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868211 | ||||||
chr9:26868222
|
TTTGTGA | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.666-7089_666-7084d others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868222 | ||||||
chr9:26868284
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.666-7145T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868284 | ||||||
chr9:26868371
|
T | C | 10 | a0001c0001t0001g0130a0001c0001t0001g0167a0001c0001t0001g0181others(7): Show | 10 | HG00423.hp2 HG02165.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-7232A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868371 | ||||||
chr9:26868402
|
C | A | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.666-7263G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868402 | ||||||
chr9:26868697
|
A | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-7558T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868697 | ||||||
chr9:26868701
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.666-7562G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868701 | ||||||
chr9:26868791
|
CAA | C | 7 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-7654_666-7653d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26868791 | ||||||
chr9:26869203
|
T | A | 27 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(24): Show | 27 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-8064A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869203 | ||||||
chr9:26869374
|
T | C | 1 | a0005c0005t0009g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.666-8235A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869374 | ||||||
chr9:26869513
|
G | GA | 5 | a0001c0001t0001g0140a0001c0001t0002g0203a0001c0002t0001g0257others(2): Show | 5 | HG01255.hp1 HG03942.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-8375dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869513 | ||||||
chr9:26869534
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(122): Show | 133 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.666-8395A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869534 | ||||||
chr9:26869599
|
G | A | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-8460C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869599 | ||||||
chr9:26869602
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-8463G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869602 | ||||||
chr9:26869621
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.666-8482T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869621 | ||||||
chr9:26869657
|
G | A | 1 | a0002c0003t0001g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.666-8518C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869657 | ||||||
chr9:26869753
|
A | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-8614T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869753 | ||||||
chr9:26869827
|
T | C | 5 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-8688A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26869827 | ||||||
chr9:26870039
|
C | CT | 16 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0121others(13): Show | 16 | HG00099.hp2 HG00735.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.666-8901dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | ||||||
chr9:26870039
|
C | CTT | 26 | a0001c0001t0001g0077a0001c0001t0001g0107a0001c0001t0001g0108others(23): Show | 26 | HG00733.hp1 HG02055.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.666-8902_666-8901d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | ||||||
chr9:26870039
|
CT | C | 30 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0071others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.666-8901delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | ||||||
chr9:26870039
|
CTT | C | 17 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(14): Show | 18 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.666-8902_666-8901d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870039 | ||||||
chr9:26870059
|
T | A | 1 | a0001c0002t0001g0341 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.666-8920A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870059 | ||||||
chr9:26870169
|
C | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0106 | 3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.666-9030G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870169 | ||||||
chr9:26870218
|
T | C | 3 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019 | 4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-9079A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870218 | ||||||
chr9:26870227
|
G | A | 4 | a0001c0002t0001g0343a0001c0002t0001g0344a0001c0002t0001g0345others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-9088C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870227 | ||||||
chr9:26870257
|
G | C | 3 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019 | 4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-9118C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870257 | ||||||
chr9:26870273
|
T | C | 1 | a0002c0003t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.666-9134A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870273 | ||||||
chr9:26870481
|
C | A | 1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666-9342G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870481 | ||||||
chr9:26870488
|
A | G | 1 | a0001c0001t0005g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.666-9349T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870488 | ||||||
chr9:26870523
|
C | T | 139 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(136): Show | 146 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.666-9384G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870523 | ||||||
chr9:26870547
|
T | TAC | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(125): Show | 136 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.666-9410_666-9409d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870547 | ||||||
chr9:26870566
|
G | A | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-9427C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870566 | ||||||
chr9:26870587
|
C | CGT | 21 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(18): Show | 21 | HG00639.hp2 HG01074.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-9450_666-9449d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | ||||||
chr9:26870587
|
C | CGTGT | 5 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.666-9452_666-9449d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | ||||||
chr9:26870587
|
CGT | C | 16 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG00323.hp1 HG01258.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.666-9450_666-9449d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | ||||||
chr9:26870587
|
CGTGT | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(146): Show | 157 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.666-9452_666-9449d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870587 | ||||||
chr9:26870677
|
C | T | 105 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(102): Show | 111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.666-9538G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870677 | ||||||
chr9:26870749
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.666-9610G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870749 | ||||||
chr9:26870766
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.666-9627C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870766 | ||||||
chr9:26870855
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.666-9716C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26870855 | ||||||
chr9:26871270
|
G | GT | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-10132dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871270 | ||||||
chr9:26871326
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | NA19009.hp2 NA19055.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-10187G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871326 | ||||||
chr9:26871480
|
G | C | 6 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(3): Show | 6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-10341C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871480 | ||||||
chr9:26871500
|
G | C | 29 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(26): Show | 30 | HG00323.hp1 HG01192.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.666-10361C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871500 | ||||||
chr9:26871501
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-10362A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871501 | ||||||
chr9:26871560
|
C | T | 106 | a0001c0001t0002g0126a0001c0002t0001g0011a0001c0002t0001g0012others(103): Show | 112 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.666-10421G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871560 | ||||||
chr9:26871577
|
T | TAA | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-10440_666-1043 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871577 | ||||||
chr9:26871577
|
TA | T | 7 | a0001c0001t0001g0087a0001c0001t0002g0203a0001c0001t0002g0228others(4): Show | 7 | HG01070.hp2 HG01255.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-10439delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871577 | ||||||
chr9:26871661
|
C | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.666-10522G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871661 | ||||||
chr9:26871662
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.666-10523C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871662 | ||||||
chr9:26871788
|
C | T | 1 | a0001c0002t0001g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.666-10649G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871788 | ||||||
chr9:26871837
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(180): Show | 192 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.666-10698A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871837 | ||||||
chr9:26871901
|
C | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-10762G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871901 | ||||||
chr9:26871914
|
A | AAAAT | 5 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0002t0001g0347others(2): Show | 6 | HG01496.hp1 HG02015.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-10779_666-1077 others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | ||||||
chr9:26871914
|
A | AAAATAAA others(5): Show |
5 | a0002c0003t0001g0027a0002c0003t0001g0028a0002c0003t0001g0029others(2): Show | 5 | HG01496.hp2 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-10787_666-1077 others(16): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | ||||||
chr9:26871914
|
A | AAAATAAA others(9): Show |
6 | a0002c0003t0001g0001a0002c0003t0001g0019a0002c0003t0001g0033others(3): Show | 7 | HG01192.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-10791_666-1077 others(20): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | ||||||
chr9:26871914
|
A | AAAATAAA others(13): Show |
5 | a0002c0003t0001g0020a0002c0003t0001g0021a0002c0003t0001g0023others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-10795_666-1077 others(24): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | ||||||
chr9:26871914
|
A | AAAATAAA others(17): Show |
1 | a0002c0003t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.666-10799_666-1077 others(28): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871914 | ||||||
chr9:26871942
|
T | TAAATAAA others(9): Show |
1 | a0002c0003t0001g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666-10804_666-1080 others(20): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871942 | ||||||
chr9:26871992
|
T | A | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(182): Show | 194 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.666-10853A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26871992 | ||||||
chr9:26872053
|
G | A | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-10914C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872053 | ||||||
chr9:26872472
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-11333G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872472 | ||||||
chr9:26872540
|
T | C | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-11401A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872540 | ||||||
chr9:26872553
|
A | AAT | 24 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(21): Show | 25 | HG01069.hp2 HG01070.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.666-11416_666-1141 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATAT | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.666-11418_666-1141 others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(9): Show |
1 | a0002c0003t0001g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.666-11430_666-1141 others(20): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(13): Show |
3 | a0002c0003t0001g0018a0002c0003t0001g0029a0002c0003t0001g0031 | 3 | HG03041.hp2 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.666-11434_666-1141 others(24): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(15): Show |
1 | a0002c0003t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(26): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(19): Show |
3 | a0002c0003t0001g0001a0002c0003t0001g0019a0002c0003t0001g0027 | 4 | HG01192.hp2 HG01496.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-11415_666-1141 others(30): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(23): Show |
1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666-11415_666-1141 others(34): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(25): Show |
1 | a0002c0003t0001g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(36): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(29): Show |
2 | a0002c0003t0001g0020a0002c0003t0001g0034 | 2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.666-11415_666-1141 others(40): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(35): Show |
1 | a0002c0003t0001g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(46): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | AATATATA others(39): Show |
1 | a0002c0003t0001g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(50): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
A | ATATATAT others(18): Show |
1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-11415_666-1141 others(29): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872553
|
AATAT | A | 3 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0032 | 3 | HG02451.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.666-11418_666-1141 others(8): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872553 | ||||||
chr9:26872573
|
T | TATATATA others(10): Show |
1 | a0002c0003t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-11435_666-1143 others(21): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872573 | ||||||
chr9:26872573
|
T | TATATATA others(36): Show |
1 | a0002c0003t0001g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.666-11435_666-1143 others(47): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872573 | ||||||
chr9:26872759
|
T | C | 13 | a0001c0001t0002g0222a0001c0001t0002g0225a0001c0001t0002g0228others(10): Show | 13 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.666-11620A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872759 | ||||||
chr9:26872767
|
A | G | 27 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(24): Show | 27 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-11628T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872767 | ||||||
chr9:26872856
|
CTTT | C | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.666-11720_666-1171 others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872856 | ||||||
chr9:26872915
|
C | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.666-11776G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872915 | ||||||
chr9:26872946
|
A | G | 1 | a0001c0002t0001g0259 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.666-11807T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872946 | ||||||
chr9:26872978
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.665+11832A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26872978 | ||||||
chr9:26873012
|
G | C | 1 | a0001c0001t0010g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.665+11798C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873012 | ||||||
chr9:26873027
|
G | A | 1 | a0005c0005t0009g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.665+11783C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873027 | ||||||
chr9:26873109
|
T | G | 17 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0257others(14): Show | 19 | HG00621.hp2 HG02015.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.665+11701A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873109 | ||||||
chr9:26873152
|
C | G | 1 | a0001c0002t0001g0299 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.665+11658G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873152 | ||||||
chr9:26873195
|
T | C | 1 | a0004c0008t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.665+11615A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873195 | ||||||
chr9:26873379
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+11431C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873379 | ||||||
chr9:26873410
|
C | A | 1 | a0001c0002t0001g0348 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.665+11400G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873410 | ||||||
chr9:26873472
|
T | C | 2 | a0001c0002t0001g0347a0001c0002t0001g0348 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665+11338A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873472 | ||||||
chr9:26873502
|
A | C | 3 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019 | 4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+11308T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873502 | ||||||
chr9:26873663
|
G | A | 3 | a0002c0003t0001g0029a0002c0003t0001g0030a0002c0003t0001g0031 | 3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.665+11147C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873663 | ||||||
chr9:26873739
|
A | G | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.665+11071T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873739 | ||||||
chr9:26873809
|
T | C | 1 | a0001c0002t0001g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.665+11001A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873809 | ||||||
chr9:26873858
|
C | T | 13 | a0001c0001t0002g0222a0001c0001t0002g0225a0001c0001t0002g0228others(10): Show | 13 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.665+10952G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873858 | ||||||
chr9:26873946
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+10864C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873946 | ||||||
chr9:26873979
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.665+10831C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26873979 | ||||||
chr9:26874076
|
A | G | 1 | a0002c0003t0001g0029 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.665+10734T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874076 | ||||||
chr9:26874100
|
G | A | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.665+10710C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874100 | ||||||
chr9:26874137
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.665+10673C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874137 | ||||||
chr9:26874206
|
C | CA | 58 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0059others(55): Show | 58 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.665+10603dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | ||||||
chr9:26874206
|
C | CAA | 9 | a0001c0001t0001g0167a0001c0001t0001g0190a0001c0001t0001g0191others(6): Show | 9 | HG00423.hp2 HG02886.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+10602_665+1060 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | ||||||
chr9:26874206
|
CA | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0048others(43): Show | 49 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.665+10603delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | ||||||
chr9:26874206
|
CAA | C | 86 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(83): Show | 90 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.665+10602_665+1060 others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | ||||||
chr9:26874206
|
CAAA | C | 8 | a0001c0001t0010g0120a0001c0002t0001g0263a0001c0002t0001g0271others(5): Show | 8 | HG01167.hp2 HG02273.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+10601_665+1060 others(7): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874206 | ||||||
chr9:26874233
|
A | T | 1 | a0001c0002t0001g0270 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.665+10577T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874233 | ||||||
chr9:26874234
|
T | A | 1 | a0001c0001t0002g0244 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.665+10576A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874234 | ||||||
chr9:26874273
|
A | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+10537T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874273 | ||||||
chr9:26874336
|
T | C | 1 | a0002c0003t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.665+10474A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874336 | ||||||
chr9:26874345
|
T | C | 29 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(26): Show | 30 | HG00323.hp1 HG01192.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.665+10465A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874345 | ||||||
chr9:26874434
|
A | G | 10 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(7): Show | 10 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+10376T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874434 | ||||||
chr9:26874484
|
C | T | 103 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(100): Show | 108 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.665+10326G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874484 | ||||||
chr9:26874559
|
C | A | 11 | a0001c0002t0001g0341a0001c0002t0001g0342a0002c0003t0001g0001others(8): Show | 12 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+10251G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874559 | ||||||
chr9:26874636
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0105 | 2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.665+10174A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874636 | ||||||
chr9:26874761
|
AAAGGAGC others(6): Show |
A | 2 | a0001c0002t0001g0304a0001c0002t0001g0332 | 2 | NA18951.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.665+10036_665+1004 others(17): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874761 | ||||||
chr9:26874812
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.665+9998C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26874812 | ||||||
chr9:26875042
|
A | G | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+9768T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875042 | ||||||
chr9:26875126
|
A | G | 2 | a0001c0002t0001g0347a0001c0002t0001g0348 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665+9684T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875126 | ||||||
chr9:26875161
|
G | T | 1 | a0001c0002t0001g0324 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.665+9649C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875161 | ||||||
chr9:26875382
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.665+9428A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875382 | ||||||
chr9:26875557
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.665+9253C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875557 | ||||||
chr9:26875646
|
CAG | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+9162_665+9163d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875646 | ||||||
chr9:26875665
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.665+9145G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875665 | ||||||
chr9:26875674
|
T | C | 1 | a0001c0002t0001g0316 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.665+9136A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875674 | ||||||
chr9:26875676
|
T | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 27 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.665+9134A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875676 | ||||||
chr9:26875788
|
G | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 27 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.665+9022C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875788 | ||||||
chr9:26875789
|
A | T | 13 | a0001c0001t0001g0072a0001c0002t0001g0314a0001c0002t0001g0316others(10): Show | 13 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.665+9021T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875789 | ||||||
chr9:26875834
|
C | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+8976G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26875834 | ||||||
chr9:26876250
|
C | T | 1 | a0001c0002t0001g0349 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665+8560G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876250 | ||||||
chr9:26876253
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0073 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.665+8557G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876253 | ||||||
chr9:26876314
|
G | A | 2 | a0001c0002t0001g0341a0001c0002t0001g0342 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.665+8496C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876314 | ||||||
chr9:26876422
|
G | C | 19 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(16): Show | 20 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.665+8388C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876422 | ||||||
chr9:26876470
|
A | AG | 32 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(29): Show | 33 | HG01069.hp2 HG01256.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.665+8339dupC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876470 | ||||||
chr9:26876472
|
G | GGT | 121 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0066others(118): Show | 128 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.665+8337_665+8338i others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | ||||||
chr9:26876472
|
G | GGTT | 3 | a0001c0002t0001g0316a0001c0002t0001g0334a0001c0002t0001g0347 | 3 | HG00438.hp2 HG02055.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.665+8337_665+8338i others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | ||||||
chr9:26876472
|
G | GT | 11 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0060others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.665+8337dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | ||||||
chr9:26876472
|
GTTT | G | 7 | a0002c0003t0001g0018a0002c0003t0001g0022a0002c0003t0001g0032others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+8335_665+8337d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | ||||||
chr9:26876472
|
GTTTT | G | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+8334_665+8337d others(6): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876472 | ||||||
chr9:26876473
|
T | G | 8 | a0001c0001t0001g0087a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+8337A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876473 | ||||||
chr9:26876475
|
T | G | 4 | a0002c0003t0001g0001a0002c0003t0001g0019a0002c0003t0001g0020others(1): Show | 5 | HG01192.hp2 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+8335A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876475 | ||||||
chr9:26876476
|
T | G | 7 | a0002c0003t0001g0018a0002c0003t0001g0022a0002c0003t0001g0032others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+8334A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876476 | ||||||
chr9:26876477
|
T | G | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+8333A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876477 | ||||||
chr9:26876481
|
T | G | 3 | a0001c0002t0001g0268a0001c0002t0001g0305a0001c0002t0001g0306 | 3 | NA18974.hp2 NA19009.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.665+8329A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876481 | ||||||
chr9:26876580
|
A | C | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+8230T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876580 | ||||||
chr9:26876592
|
T | C | 6 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(3): Show | 6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+8218A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876592 | ||||||
chr9:26876658
|
T | G | 6 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(3): Show | 6 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+8152A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26876658 | ||||||
chr9:26877008
|
G | A | 2 | a0001c0002t0001g0347a0001c0002t0001g0348 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665+7802C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877008 | ||||||
chr9:26877022
|
C | G | 2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.665+7788G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877022 | ||||||
chr9:26877184
|
C | G | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+7626G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877184 | ||||||
chr9:26877261
|
T | C | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+7549A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877261 | ||||||
chr9:26877403
|
C | T | 1 | a0001c0002t0001g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.665+7407G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877403 | ||||||
chr9:26877750
|
C | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02615.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.665+7060G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877750 | ||||||
chr9:26877885
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.665+6925T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877885 | ||||||
chr9:26877888
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+6922A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877888 | ||||||
chr9:26877894
|
AATT | A | 21 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(18): Show | 21 | HG00733.hp1 HG01256.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.665+6913_665+6915d others(5): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877894 | ||||||
chr9:26877993
|
G | A | 1 | a0001c0002t0001g0307 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.665+6817C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26877993 | ||||||
chr9:26878045
|
A | C | 1 | a0001c0001t0002g0010 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.665+6765T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878045 | ||||||
chr9:26878103
|
A | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+6707T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878103 | ||||||
chr9:26878105
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+6705A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878105 | ||||||
chr9:26878147
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.665+6663T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878147 | ||||||
chr9:26878297
|
A | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 27 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.665+6513T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878297 | ||||||
chr9:26878376
|
G | C | 35 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(32): Show | 35 | HG00408.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.665+6434C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878376 | ||||||
chr9:26878471
|
T | C | 1 | a0001c0002t0001g0323 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.665+6339A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878471 | ||||||
chr9:26878678
|
T | A | 1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.665+6132A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878678 | ||||||
chr9:26878813
|
TA | T | 11 | a0001c0001t0001g0168a0002c0003t0001g0022a0002c0003t0001g0023others(8): Show | 11 | HG01496.hp2 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+5996delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878813 | ||||||
chr9:26878813
|
TAA | T | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+5995_665+5996d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878813 | ||||||
chr9:26878979
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.665+5831G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26878979 | ||||||
chr9:26879208
|
T | C | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665+5602A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879208 | ||||||
chr9:26879230
|
T | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+5580A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879230 | ||||||
chr9:26879375
|
C | G | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | HG00423.hp1 HG02080.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+5435G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879375 | ||||||
chr9:26879421
|
T | C | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665+5389A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879421 | ||||||
chr9:26879536
|
T | C | 1 | a0002c0003t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.665+5274A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879536 | ||||||
chr9:26879855
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4955G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879855 | ||||||
chr9:26879860
|
G | T | 1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.665+4950C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879860 | ||||||
chr9:26879900
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4910A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879900 | ||||||
chr9:26879938
|
G | C | 1 | a0001c0001t0001g0058 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.665+4872C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26879938 | ||||||
chr9:26880074
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+4736G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880074 | ||||||
chr9:26880092
|
T | A | 1 | a0001c0002t0001g0308 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.665+4718A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880092 | ||||||
chr9:26880093
|
C | T | 1 | a0001c0002t0001g0308 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.665+4717G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880093 | ||||||
chr9:26880093
|
CCG | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0106 | 3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.665+4715_665+4716d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880093 | ||||||
chr9:26880094
|
CG | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0077others(116): Show | 126 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.665+4715delC | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880094 | ||||||
chr9:26880094
|
CGG | C | 161 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.665+4714_665+4715d others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880094 | ||||||
chr9:26880095
|
G | C | 1 | a0001c0002t0001g0308 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.665+4715C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880095 | ||||||
chr9:26880095
|
G | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.665+4715C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880095 | ||||||
chr9:26880096
|
G | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0106 | 3 | NA18960.hp1 NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.665+4714C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880096 | ||||||
chr9:26880101
|
G | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+4709C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880101 | ||||||
chr9:26880107
|
T | G | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+4703A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880107 | ||||||
chr9:26880173
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4637C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880173 | ||||||
chr9:26880224
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4586G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880224 | ||||||
chr9:26880242
|
A | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4568T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880242 | ||||||
chr9:26880337
|
C | T | 1 | a0002c0003t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.665+4473G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880337 | ||||||
chr9:26880343
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+4467C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880343 | ||||||
chr9:26880419
|
G | A | 1 | a0006c0009t0001g0139 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.665+4391C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880419 | ||||||
chr9:26880459
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+4351C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880459 | ||||||
chr9:26880554
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0066others(111): Show | 121 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.665+4256A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880554 | ||||||
chr9:26880770
|
G | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG02630.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.665+4040C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880770 | ||||||
chr9:26880886
|
C | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(181): Show | 193 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.665+3924G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880886 | ||||||
chr9:26880920
|
A | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+3890T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26880920 | ||||||
chr9:26881101
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(169): Show | 181 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.665+3709T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881101 | ||||||
chr9:26881188
|
G | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0166a0001c0001t0001g0194others(5): Show | 8 | HG02129.hp2 HG02132.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+3622C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881188 | ||||||
chr9:26881273
|
C | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(7): Show | 11 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.665+3537G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881273 | ||||||
chr9:26881301
|
A | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+3509T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881301 | ||||||
chr9:26881362
|
A | G | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+3448T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881362 | ||||||
chr9:26881365
|
T | G | 1 | a0001c0002t0001g0309 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.665+3445A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881365 | ||||||
chr9:26881537
|
C | T | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+3273G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881537 | ||||||
chr9:26881595
|
T | C | 1 | a0001c0002t0001g0310 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.665+3215A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881595 | ||||||
chr9:26881729
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.665+3081G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881729 | ||||||
chr9:26881838
|
G | T | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+2972C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881838 | ||||||
chr9:26881864
|
T | A | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.665+2946A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881864 | ||||||
chr9:26881901
|
C | T | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(344): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.665+2909G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26881901 | ||||||
chr9:26882245
|
G | A | 1 | a0001c0002t0001g0011 | 2 | HG02015.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.665+2565C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882245 | ||||||
chr9:26882438
|
T | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+2372A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882438 | ||||||
chr9:26882459
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.665+2351A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882459 | ||||||
chr9:26882536
|
T | C | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+2274A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882536 | ||||||
chr9:26882541
|
T | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.665+2269A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882541 | ||||||
chr9:26882586
|
G | A | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.665+2224C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882586 | ||||||
chr9:26882600
|
G | A | 1 | a0001c0001t0007g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.665+2210C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882600 | ||||||
chr9:26882614
|
C | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.665+2196G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882614 | ||||||
chr9:26882631
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.665+2179G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882631 | ||||||
chr9:26882672
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+2138G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882672 | ||||||
chr9:26882814
|
T | C | 1 | a0003c0004t0001g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.665+1996A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882814 | ||||||
chr9:26882994
|
C | A | 1 | a0002c0003t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.665+1816G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26882994 | ||||||
chr9:26883001
|
A | G | 2 | a0001c0002t0001g0343a0001c0002t0001g0346 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.665+1809T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883001 | ||||||
chr9:26883048
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0158others(7): Show | 12 | HG00733.hp2 HG01081.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.665+1762G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883048 | ||||||
chr9:26883049
|
G | A | 2 | a0001c0001t0001g0201a0001c0002t0001g0311 | 2 | HG02698.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.665+1761C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883049 | ||||||
chr9:26883096
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(156): Show | 167 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.665+1714A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883096 | ||||||
chr9:26883151
|
C | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(165): Show | 177 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.665+1659G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883151 | ||||||
chr9:26883158
|
C | T | 1 | a0002c0007t0011g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665+1652G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883158 | ||||||
chr9:26883204
|
C | T | 3 | a0001c0001t0001g0045a0001c0002t0001g0341a0001c0002t0001g0342 | 3 | HG01167.hp2 HG01169.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.665+1606G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883204 | ||||||
chr9:26883361
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.665+1449C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883361 | ||||||
chr9:26883686
|
A | T | 1 | a0001c0001t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.665+1124T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883686 | ||||||
chr9:26883701
|
C | T | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+1109G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883701 | ||||||
chr9:26883704
|
C | T | 1 | a0002c0003t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.665+1106G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883704 | ||||||
chr9:26883846
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0200 | 3 | NA18998.hp1 NA19002.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.665+964A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26883846 | ||||||
chr9:26884047
|
T | C | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+763A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884047 | ||||||
chr9:26884100
|
C | A | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+710G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884100 | ||||||
chr9:26884268
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.665+542A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884268 | ||||||
chr9:26884307
|
A | T | 2 | a0001c0002t0001g0261a0001c0002t0001g0263 | 2 | NA18747.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.665+503T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884307 | ||||||
chr9:26884364
|
C | T | 2 | a0001c0002t0001g0261a0001c0002t0001g0263 | 2 | NA18747.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.665+446G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884364 | ||||||
chr9:26884410
|
C | A | 1 | a0001c0001t0010g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.665+400G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884410 | ||||||
chr9:26884459
|
T | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+351A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884459 | ||||||
chr9:26884477
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.665+333G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884477 | ||||||
chr9:26884506
|
A | G | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665+304T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884506 | ||||||
chr9:26884543
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.665+267C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884543 | ||||||
chr9:26884546
|
G | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+264C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884546 | ||||||
chr9:26884594
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.665+216C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884594 | ||||||
chr9:26884706
|
T | C | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+104A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884706 | ||||||
chr9:26884739
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.665+71G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 4/5 | chr9 | 26884739 | ||||||
chr9:26885013
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.590-128T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885013 | ||||||
chr9:26885041
|
T | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.590-156A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885041 | ||||||
chr9:26885074
|
C | CT | 19 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0059others(16): Show | 20 | HG01243.hp2 HG01928.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.590-190dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885074 | ||||||
chr9:26885074
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.590-189G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885074 | ||||||
chr9:26885074
|
CT | C | 23 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0001g0153others(20): Show | 24 | HG01192.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.590-190delA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885074 | ||||||
chr9:26885075
|
T | C | 1 | a0001c0001t0004g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.590-190A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885075 | ||||||
chr9:26885076
|
T | C | 1 | a0001c0001t0004g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.590-191A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885076 | ||||||
chr9:26885095
|
T | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA19077.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.590-210A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885095 | ||||||
chr9:26885099
|
C | G | 1 | a0007c0006t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.590-214G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885099 | ||||||
chr9:26885099
|
C | T | 1 | a0002c0003t0001g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.590-214G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885099 | ||||||
chr9:26885121
|
G | A | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.590-236C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885121 | ||||||
chr9:26885169
|
C | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0134others(128): Show | 138 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.590-284G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885169 | ||||||
chr9:26885203
|
A | C | 1 | a0001c0001t0002g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.590-318T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885203 | ||||||
chr9:26885212
|
G | A | 2 | a0002c0003t0001g0027a0002c0003t0001g0028 | 2 | HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.590-327C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885212 | ||||||
chr9:26885261
|
G | C | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.590-376C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885261 | ||||||
chr9:26885292
|
G | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.590-407C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885292 | ||||||
chr9:26885297
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.590-412C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885297 | ||||||
chr9:26885354
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0136 | 2 | HG01192.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.590-469G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885354 | ||||||
chr9:26885370
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.590-485G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885370 | ||||||
chr9:26885371
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.590-486C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885371 | ||||||
chr9:26885406
|
G | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(7): Show | 11 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.590-521C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885406 | ||||||
chr9:26885661
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.589+443C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885661 | ||||||
chr9:26885681
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.589+423A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885681 | ||||||
chr9:26885775
|
C | T | 22 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(19): Show | 22 | HG00733.hp1 HG01256.hp2 HG02615.hp2 others(19): Show |
intron_variant | MODIFIER | c.589+329G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885775 | ||||||
chr9:26885822
|
T | C | 17 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(14): Show | 17 | HG00733.hp1 HG01256.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+282A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885822 | ||||||
chr9:26885824
|
A | AT | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.589+279dupA | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885824 | ||||||
chr9:26885935
|
T | C | 1 | a0001c0002t0001g0256 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.589+169A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885935 | ||||||
chr9:26885941
|
T | C | 1 | a0003c0004t0001g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.589+163A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885941 | ||||||
chr9:26885992
|
A | C | 12 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(9): Show | 12 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+112T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 3/5 | chr9 | 26885992 | ||||||
chr9:26886230
|
C | T | 1 | a0001c0002t0001g0314 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.505-42G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886230 | ||||||
chr9:26886395
|
C | T | 94 | a0001c0001t0002g0126a0001c0002t0001g0011a0001c0002t0001g0012others(91): Show | 100 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.505-207G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886395 | ||||||
chr9:26886546
|
T | G | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.505-358A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886546 | ||||||
chr9:26886551
|
A | T | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(344): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.505-363T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886551 | ||||||
chr9:26886587
|
A | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(7): Show | 11 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.505-399T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886587 | ||||||
chr9:26886780
|
C | T | 1 | a0001c0002t0001g0260 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.504+533G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886780 | ||||||
chr9:26886793
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0066others(105): Show | 115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.504+520A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886793 | ||||||
chr9:26886822
|
A | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.504+491T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886822 | ||||||
chr9:26886934
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.504+379G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886934 | ||||||
chr9:26886939
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.504+374C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886939 | ||||||
chr9:26886997
|
C | A | 1 | a0001c0001t0001g0009 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.504+316G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26886997 | ||||||
chr9:26887069
|
G | A | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.504+244C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26887069 | ||||||
chr9:26887113
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.504+200C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26887113 | ||||||
chr9:26887300
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.504+13A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 2/5 | chr9 | 26887300 | ||||||
chr9:26887537
|
C | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.304-24G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887537 | ||||||
chr9:26887585
|
A | G | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.304-72T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887585 | ||||||
chr9:26887738
|
T | C | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.304-225A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887738 | ||||||
chr9:26887758
|
A | C | 1 | a0002c0003t0001g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.304-245T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887758 | ||||||
chr9:26887898
|
G | C | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.304-385C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887898 | ||||||
chr9:26887978
|
T | C | 39 | a0001c0001t0001g0241a0001c0001t0002g0010a0001c0001t0002g0124others(36): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.304-465A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26887978 | ||||||
chr9:26888070
|
C | T | 1 | a0002c0003t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.304-557G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888070 | ||||||
chr9:26888176
|
CTGTTAGC others(4): Show |
C | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.304-674_304-664del others(11): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888176 | ||||||
chr9:26888209
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-696C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888209 | ||||||
chr9:26888328
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.304-815G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888328 | ||||||
chr9:26888434
|
C | A | 1 | a0001c0002t0001g0354 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.304-921G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888434 | ||||||
chr9:26888548
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-1035A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888548 | ||||||
chr9:26888741
|
G | C | 1 | a0005c0005t0009g0017 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.304-1228C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888741 | ||||||
chr9:26888747
|
T | C | 1 | a0001c0001t0008g0206 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.304-1234A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888747 | ||||||
chr9:26888789
|
T | C | 3 | a0003c0004t0001g0097a0003c0004t0001g0252a0003c0004t0001g0253 | 3 | HG01884.hp1 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.304-1276A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888789 | ||||||
chr9:26888901
|
T | C | 1 | a0001c0002t0001g0323 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.304-1388A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888901 | ||||||
chr9:26888968
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.304-1455T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26888968 | ||||||
chr9:26889031
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-1518T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889031 | ||||||
chr9:26889136
|
G | A | 24 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0108others(21): Show | 24 | HG00733.hp1 HG01256.hp2 HG02615.hp2 others(21): Show |
intron_variant | MODIFIER | c.304-1623C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889136 | ||||||
chr9:26889246
|
G | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-1733C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889246 | ||||||
chr9:26889269
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.304-1756A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889269 | ||||||
chr9:26889287
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1774C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889287 | ||||||
chr9:26889313
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.304-1800C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889313 | ||||||
chr9:26889409
|
A | G | 1 | a0002c0003t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.304-1896T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889409 | ||||||
chr9:26889420
|
AAAAAACA others(5): Show |
A | 1 | a0002c0003t0001g0019 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.304-1919_304-1908d others(14): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889420 | ||||||
chr9:26889565
|
G | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-2052C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889565 | ||||||
chr9:26889636
|
G | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-2123C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889636 | ||||||
chr9:26889697
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.304-2184G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889697 | ||||||
chr9:26889746
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.304-2233A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889746 | ||||||
chr9:26889781
|
T | C | 2 | a0001c0002t0001g0336a0001c0002t0001g0337 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.304-2268A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889781 | ||||||
chr9:26889793
|
A | G | 1 | a0001c0002t0001g0259 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.304-2280T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889793 | ||||||
chr9:26889807
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.304-2294C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889807 | ||||||
chr9:26889831
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.304-2318C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889831 | ||||||
chr9:26889855
|
G | A | 1 | a0001c0001t0002g0010 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.304-2342C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889855 | ||||||
chr9:26889866
|
T | C | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01361.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-2353A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889866 | ||||||
chr9:26889867
|
C | CA | 66 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(63): Show | 67 | HG00621.hp1 HG00733.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.304-2355dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889867 | ||||||
chr9:26889897
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 12 | HG01069.hp2 HG01070.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-2384G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889897 | ||||||
chr9:26889958
|
T | C | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.304-2445A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889958 | ||||||
chr9:26889981
|
T | C | 3 | a0002c0003t0001g0029a0002c0003t0001g0030a0002c0003t0001g0031 | 3 | HG03041.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.303+2432A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889981 | ||||||
chr9:26889995
|
A | T | 1 | a0001c0001t0001g0037 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.303+2418T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26889995 | ||||||
chr9:26890090
|
T | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+2323A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890090 | ||||||
chr9:26890126
|
T | A | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+2287A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890126 | ||||||
chr9:26890127
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02895.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.303+2286A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890127 | ||||||
chr9:26890328
|
G | A | 3 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019 | 4 | HG01192.hp2 HG02280.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+2085C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890328 | ||||||
chr9:26890360
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.303+2053C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890360 | ||||||
chr9:26890378
|
G | GA | 35 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0002g0010others(32): Show | 36 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.303+2034dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890378 | ||||||
chr9:26890378
|
GA | G | 21 | a0001c0002t0001g0258a0002c0003t0001g0001a0002c0003t0001g0018others(18): Show | 22 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.303+2034delT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890378 | ||||||
chr9:26890570
|
A | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.303+1843T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890570 | ||||||
chr9:26890576
|
C | T | 8 | a0002c0003t0001g0024a0002c0003t0001g0027a0002c0003t0001g0028others(5): Show | 8 | HG01496.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+1837G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890576 | ||||||
chr9:26890805
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0005g0131 | 2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.303+1608G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890805 | ||||||
chr9:26890837
|
C | T | 1 | a0002c0003t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.303+1576G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890837 | ||||||
chr9:26890874
|
G | A | 1 | a0001c0002t0001g0339 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.303+1539C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890874 | ||||||
chr9:26890876
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.303+1537G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890876 | ||||||
chr9:26890921
|
G | A | 1 | a0001c0002t0001g0340 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.303+1492C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890921 | ||||||
chr9:26890953
|
C | CA | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 24 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.303+1459dupT | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26890953 | ||||||
chr9:26891097
|
C | T | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+1316G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891097 | ||||||
chr9:26891237
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1176T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891237 | ||||||
chr9:26891238
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1175T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891238 | ||||||
chr9:26891241
|
G | C | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1172C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891241 | ||||||
chr9:26891242
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1171G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891242 | ||||||
chr9:26891243
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1170T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891243 | ||||||
chr9:26891245
|
A | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0082others(178): Show | 189 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.303+1168T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891245 | ||||||
chr9:26891247
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1166T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891247 | ||||||
chr9:26891248
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303+1165T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891248 | ||||||
chr9:26891301
|
C | CAA | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+1111_303+1112i others(4): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891301 | ||||||
chr9:26891335
|
T | A | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.303+1078A>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891335 | ||||||
chr9:26891566
|
CACA | C | 97 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(94): Show | 103 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.303+844_303+846del others(3): Show |
CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891566 | ||||||
chr9:26891766
|
G | C | 105 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(102): Show | 111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.303+647C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891766 | ||||||
chr9:26891789
|
G | A | 2 | a0001c0001t0002g0250a0001c0001t0002g0251 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.303+624C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891789 | ||||||
chr9:26891829
|
T | C | 2 | a0003c0004t0001g0252a0003c0004t0001g0253 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.303+584A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891829 | ||||||
chr9:26891831
|
G | C | 20 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(17): Show | 21 | HG01192.hp2 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303+582C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891831 | ||||||
chr9:26891861
|
T | C | 2 | a0002c0003t0001g0022a0002c0003t0001g0032 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.303+552A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891861 | ||||||
chr9:26891904
|
T | G | 105 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(102): Show | 111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.303+509A>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26891904 | ||||||
chr9:26892015
|
G | T | 2 | a0001c0002t0001g0011a0001c0002t0001g0257 | 3 | HG02015.hp2 NA18945.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.303+398C>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892015 | ||||||
chr9:26892049
|
C | G | 1 | a0002c0003t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.303+364G>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892049 | ||||||
chr9:26892075
|
G | A | 7 | a0001c0002t0001g0016a0001c0002t0001g0349a0001c0002t0001g0350others(4): Show | 8 | HG02300.hp2 HG03017.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+338C>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892075 | ||||||
chr9:26892097
|
G | C | 2 | a0002c0003t0001g0020a0002c0003t0001g0021 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.303+316C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892097 | ||||||
chr9:26892136
|
A | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.303+277T>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892136 | ||||||
chr9:26892139
|
G | C | 315 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(312): Show | 330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.303+274C>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892139 | ||||||
chr9:26892185
|
A | T | 9 | a0002c0003t0001g0001a0002c0003t0001g0018a0002c0003t0001g0019others(6): Show | 10 | HG01192.hp2 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+228T>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892185 | ||||||
chr9:26892221
|
T | C | 4 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+192A>G | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892221 | ||||||
chr9:26892303
|
A | G | 125 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(122): Show | 132 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.303+110T>C | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892303 | ||||||
chr9:26892325
|
C | T | 1 | a0001c0002t0001g0256 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.303+88G>A | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892325 | ||||||
chr9:26892337
|
C | A | 2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.303+76G>T | CAAP1 | ENSG00000120159.13 | transcript | ENST00000333916.8 | protein_coding | 1/5 | chr9 | 26892337 |