geneid | 55749 |
---|---|
ensemblid | ENSG00000060339.14 |
hgncid | 24236 |
symbol | CCAR1 |
name | cell division cycle and apoptosis regulator 1 |
refseq_nuc | NM_018237.4 |
refseq_prot | NP_060707.2 |
ensembl_nuc | ENST00000265872.11 |
ensembl_prot | ENSP00000265872.6 |
mane_status | MANE Select |
chr | chr10 |
start | 68721239 |
end | 68792377 |
strand | + |
ver | v1.2 |
region | chr10:68721239-68792377 |
region5000 | chr10:68716239-68797377 |
regionname0 | CCAR1_chr10_68721239_68792377 |
regionname5000 | CCAR1_chr10_68716239_68797377 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1150 | 357 | 82 | 60 | 162 | 14 | 37 | 128 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0002 | 0/0 | 1150 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0003 | 0/0 | 1150 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3453 | 238 | 50 | 49 | 102 | 9 | 27 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0002 | 1/0 | 3453 | 70 | 10 | 3 | 48 | 2 | 6 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0003 | 0/0 | 3453 | 37 | 21 | 5 | 10 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0004 | 0/0 | 3453 | 8 | 0 | 2 | 0 | 3 | 3 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0005 | 0/0 | 3453 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0006 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0007 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0008 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0009 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
c0010 | 0/0 | 3453 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1206 | 300 | 60 | 48 | 142 | 12 | 36 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0002 | 0/0 | 1206 | 27 | 12 | 5 | 9 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0003 | 0/0 | 1206 | 8 | 0 | 0 | 8 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0004 | 0/0 | 1204 | 5 | 5 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0005 | 0/0 | 1206 | 3 | 0 | 2 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0006 | 0/0 | 1206 | 2 | 0 | 2 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0007 | 0/0 | 1206 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0008 | 0/0 | 1206 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0009 | 0/0 | 1206 | 2 | 0 | 1 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0010 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0011 | 0/0 | 1206 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0012 | 0/0 | 1206 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0013 | 0/0 | 1206 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0014 | 0/0 | 1204 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0015 | 0/0 | 1206 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0016 | 0/0 | 1206 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0017 | 0/0 | 1206 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
t0018 | 0/0 | 1206 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3453 | 238 | 50 | 49 | 102 | 9 | 27 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0002 | 1/0 | 3453 | 70 | 10 | 3 | 48 | 2 | 6 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0003 | 0/0 | 3453 | 37 | 21 | 5 | 10 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0004 | 0/0 | 3453 | 8 | 0 | 2 | 0 | 3 | 3 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0007 | 0/0 | 3453 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0008 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0009 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0010 | 0/0 | 3453 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0002c0005 | 0/0 | 3453 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0003c0006 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4658 | 219 | 46 | 45 | 93 | 8 | 26 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0003 | 0/0 | 4658 | 8 | 0 | 0 | 8 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0005 | 0/0 | 4658 | 3 | 0 | 2 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0007 | 0/0 | 4658 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0009 | 0/0 | 4658 | 2 | 0 | 1 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0010 | 0/0 | 4658 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0015 | 0/0 | 4658 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0016 | 0/0 | 4658 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0001t0018 | 0/0 | 4658 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0002t0001 | 1/0 | 4658 | 69 | 10 | 3 | 47 | 2 | 6 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0002t0011 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0003t0001 | 0/0 | 4658 | 3 | 3 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0003t0002 | 0/0 | 4658 | 27 | 12 | 5 | 9 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0003t0004 | 0/0 | 4656 | 5 | 5 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0003t0014 | 0/0 | 4656 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0003t0017 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0004t0001 | 0/0 | 4658 | 5 | 0 | 0 | 0 | 2 | 3 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0004t0006 | 0/0 | 4658 | 2 | 0 | 2 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0004t0012 | 0/0 | 4658 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0007t0001 | 0/0 | 4658 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0008t0001 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0009t0001 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0001c0010t0013 | 0/0 | 4658 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0002c0005t0008 | 0/0 | 4658 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
a0003c0006t0001 | 0/0 | 4658 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | copy fasta | chr10 | 68716239 | 68797377 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0007g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0010g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0015g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0016g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0001t0018g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0002t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0003t0017g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0006g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0004t0012g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0007t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0008t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0009t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0001c0010t0013g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0002c0005t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0002c0005t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
a0003c0006t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0327 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00140 | hp1 | a0001 | c0004 | t0012 | g0270 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0101 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | FIN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0352 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00639 | hp2 | a0001 | c0003 | t0002 | g0047 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0065 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01168 | hp1 | a0001 | c0010 | t0013 | g0267 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01256 | hp2 | a0001 | c0004 | t0006 | g0269 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0029 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01346 | hp1 | a0001 | c0004 | t0006 | g0268 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01346 | hp2 | a0001 | c0001 | t0009 | g0013 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01433 | hp2 | a0001 | c0003 | t0002 | g0056 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0240 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0048 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01515 | hp1 | a0001 | c0004 | t0001 | g0265 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0266 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01891 | hp2 | a0002 | c0005 | t0008 | g0050 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02015 | hp2 | a0001 | c0003 | t0002 | g0052 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02074 | hp1 | a0001 | c0003 | t0002 | g0055 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02083 | hp2 | a0001 | c0003 | t0002 | g0053 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02135 | hp2 | a0001 | c0008 | t0001 | g0284 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | CDX | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0058 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0351 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02451 | hp1 | a0002 | c0005 | t0008 | g0049 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02572 | hp1 | a0001 | c0003 | t0002 | g0059 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0339 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0353 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02647 | hp1 | a0001 | c0003 | t0002 | g0075 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02647 | hp2 | a0001 | c0003 | t0004 | g0068 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02683 | hp2 | a0001 | c0003 | t0002 | g0054 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02698 | hp2 | a0003 | c0006 | t0001 | g0290 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02717 | hp1 | a0001 | c0001 | t0018 | g0088 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02809 | hp1 | a0001 | c0003 | t0002 | g0076 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02886 | hp1 | a0001 | c0003 | t0004 | g0072 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0066 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02922 | hp1 | a0001 | c0003 | t0004 | g0067 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02922 | hp2 | a0001 | c0007 | t0001 | g0280 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0073 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03098 | hp1 | a0001 | c0003 | t0014 | g0069 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0063 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0271 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0077 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04115 | hp2 | a0001 | c0001 | t0009 | g0261 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04199 | hp1 | a0001 | c0004 | t0001 | g0322 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04204 | hp1 | a0001 | c0004 | t0001 | g0272 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18947 | hp1 | a0001 | c0003 | t0002 | g0080 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18985 | hp2 | a0001 | c0003 | t0017 | g0046 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18993 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19002 | hp2 | a0001 | c0003 | t0002 | g0078 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19005 | hp2 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0338 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0062 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19043 | hp2 | a0001 | c0003 | t0004 | g0071 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19064 | hp2 | a0001 | c0009 | t0001 | g0181 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19067 | hp1 | a0001 | c0003 | t0002 | g0060 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19079 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19088 | hp1 | a0001 | c0002 | t0011 | g0146 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0337 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20129 | hp1 | a0001 | c0003 | t0002 | g0061 | AFR | ASW | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20752 | hp1 | a0001 | c0001 | t0016 | g0028 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0102 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02486 | hp2 | a0001 | c0003 | t0002 | g0074 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02559 | hp1 | a0001 | c0003 | t0004 | g0070 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0350 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0064 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0230 | REF | REF | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0090 | REF | REF | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:68737865
|
G | C | 1 | a0003 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.267G>C | p.Gln89His | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/25 | 361/4658 | 267/3453 | 89/1150 | chr10 | 68737865 | ||
chr10:68787948
|
G | A | 1 | a0002 | 2 | HG01891.hp2 HG02451.hp1 |
missense_variant | MODERATE | c.2902G>A | p.Val968Ile | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 22/25 | 2996/4658 | 2902/3453 | 968/1150 | chr10 | 68787948 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:68742435
|
A | T | 1 | a0001c0010 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.384A>T | p.Ile128Ile | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/25 | 478/4658 | 384/3453 | 128/1150 | chr10 | 68742435 | ||
chr10:68742522
|
A | G | 1 | a0001c0009 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.471A>G | p.Leu157Leu | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/25 | 565/4658 | 471/3453 | 157/1150 | chr10 | 68742522 | ||
chr10:68742531
|
G | A | 9 | a0001c0001a0001c0003a0001c0004others(6): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
synonymous_variant | LOW | c.480G>A | p.Thr160Thr | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/25 | 574/4658 | 480/3453 | 160/1150 | chr10 | 68742531 | ||
chr10:68749182
|
G | A | 1 | a0001c0007 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.873G>A | p.Pro291Pro | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 9/25 | 967/4658 | 873/3453 | 291/1150 | chr10 | 68749182 | ||
chr10:68753927
|
A | G | 2 | a0001c0003a0002c0005 | 39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
synonymous_variant | LOW | c.1194A>G | p.Gln398Gln | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/25 | 1288/4658 | 1194/3453 | 398/1150 | chr10 | 68753927 | ||
chr10:68788318
|
A | G | 1 | a0001c0008 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.3177A>G | p.Glu1059Glu | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/25 | 3271/4658 | 3177/3453 | 1059/1150 | chr10 | 68788318 | ||
chr10:68789822
|
G | A | 2 | a0001c0004a0001c0010 | 9 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(6): Show |
synonymous_variant | LOW | c.3300G>A | p.Ser1100Ser | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/25 | 3394/4658 | 3300/3453 | 1100/1150 | chr10 | 68789822 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:68721263
|
T | G | 1 | a0001c0001t0010 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/25 | 1242 | chr10 | 68721263 | |||||
chr10:68721266
|
G | C | 1 | a0001c0002t0011 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/25 | 1239 | chr10 | 68721266 | |||||
chr10:68721278
|
C | T | 1 | a0001c0001t0018 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/25 | 1227 | chr10 | 68721278 | |||||
chr10:68722481
|
G | A | 3 | a0001c0004t0006a0001c0004t0012a0001c0010t0013 | 4 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-24G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/25 | 24 | chr10 | 68722481 | |||||
chr10:68791291
|
T | C | 1 | a0001c0001t0007 | 2 | HG02280.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 25 | chr10 | 68791291 | |||||
chr10:68791475
|
T | C | 1 | a0002c0005t0008 | 2 | HG01891.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*209T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 209 | chr10 | 68791475 | |||||
chr10:68791520
|
T | C | 1 | a0001c0003t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 254 | chr10 | 68791520 | |||||
chr10:68791596
|
C | G | 5 | a0001c0003t0002a0001c0003t0004a0001c0003t0014others(2): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*330C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 330 | chr10 | 68791596 | |||||
chr10:68791663
|
CAA | C | 2 | a0001c0003t0004a0001c0003t0014 | 6 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*400_*401delAA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 400 | INFO_REALIGN_3_PRIME | chr10 | 68791663 | ||||
chr10:68791836
|
C | T | 1 | a0001c0001t0016 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*570C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 570 | chr10 | 68791836 | |||||
chr10:68791898
|
C | T | 5 | a0001c0003t0002a0001c0003t0004a0001c0003t0014others(2): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*632C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 632 | chr10 | 68791898 | |||||
chr10:68791985
|
C | T | 1 | a0001c0001t0009 | 2 | HG01346.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 719 | chr10 | 68791985 | |||||
chr10:68791986
|
G | A | 1 | a0001c0001t0003 | 8 | NA18939.hp2 NA18941.hp1 NA18954.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*720G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 720 | chr10 | 68791986 | |||||
chr10:68792017
|
C | T | 1 | a0001c0001t0015 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 751 | chr10 | 68792017 | |||||
chr10:68792133
|
A | G | 1 | a0001c0001t0005 | 3 | HG01069.hp2 HG01496.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*867A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 867 | chr10 | 68792133 | |||||
chr10:68792144
|
G | A | 2 | a0001c0004t0012a0001c0010t0013 | 2 | HG00140.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*878G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 878 | chr10 | 68792144 | |||||
chr10:68792196
|
A | C | 1 | a0001c0003t0017 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*930A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 930 | chr10 | 68792196 | |||||
chr10:68792281
|
G | A | 1 | a0001c0004t0012 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 1015 | chr10 | 68792281 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:68721328
|
G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51+46G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721328 | ||||||
chr10:68721379
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-51+97G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721379 | ||||||
chr10:68721415
|
C | T | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-51+133C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721415 | ||||||
chr10:68721431
|
G | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG01257.hp2 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+149G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721431 | ||||||
chr10:68721457
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-51+175G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721457 | ||||||
chr10:68721497
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-51+215C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721497 | ||||||
chr10:68721632
|
G | A | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-51+350G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721632 | ||||||
chr10:68721680
|
C | T | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-51+398C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721680 | ||||||
chr10:68721681
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-51+399C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721681 | ||||||
chr10:68721696
|
G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51+414G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721696 | ||||||
chr10:68721790
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-51+508C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721790 | ||||||
chr10:68721923
|
C | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-50-532C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721923 | ||||||
chr10:68722036
|
T | A | 33 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-50-419T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722036 | ||||||
chr10:68722039
|
C | A | 33 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-50-416C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722039 | ||||||
chr10:68722094
|
A | T | 1 | a0001c0002t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-50-361A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722094 | ||||||
chr10:68722396
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-50-59T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722396 | ||||||
chr10:68722612
|
G | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+35G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722612 | ||||||
chr10:68722619
|
A | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+42A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722619 | ||||||
chr10:68722647
|
G | C | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+70G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722647 | ||||||
chr10:68722661
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+84A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722661 | ||||||
chr10:68722772
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+195A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722772 | ||||||
chr10:68722936
|
A | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.73+359A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722936 | ||||||
chr10:68722980
|
T | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(40): Show | 44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.73+403T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722980 | ||||||
chr10:68723043
|
C | G | 54 | a0001c0002t0001g0006a0001c0002t0001g0109a0001c0002t0001g0110others(51): Show | 54 | HG00544.hp1 HG02040.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.73+466C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723043 | ||||||
chr10:68723057
|
T | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+480T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723057 | ||||||
chr10:68723078
|
T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+501T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723078 | ||||||
chr10:68723118
|
A | G | 1 | a0001c0001t0001g0349 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.73+541A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723118 | ||||||
chr10:68723185
|
A | G | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+608A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723185 | ||||||
chr10:68723223
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.73+646G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723223 | ||||||
chr10:68723288
|
A | AT | 9 | a0001c0001t0001g0087a0001c0001t0001g0342a0001c0001t0001g0343others(6): Show | 9 | HG01109.hp2 HG01175.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.73+725dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723288 | |||||
chr10:68723288
|
A | ATT | 71 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(68): Show | 71 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.73+724_73+725dupTT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723288 | |||||
chr10:68723317
|
G | A | 60 | a0001c0002t0001g0006a0001c0002t0001g0091a0001c0002t0001g0092others(57): Show | 60 | HG00544.hp1 HG02040.hp1 HG02055.hp2 others(57): Show |
intron_variant | MODIFIER | c.73+740G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723317 | ||||||
chr10:68723380
|
C | T | 3 | a0001c0003t0002g0075a0001c0003t0002g0076a0001c0003t0002g0077 | 3 | HG02647.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.73+803C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723380 | ||||||
chr10:68723389
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.73+812G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723389 | ||||||
chr10:68723413
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.73+836G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723413 | ||||||
chr10:68723425
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.73+848G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723425 | ||||||
chr10:68723571
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+994G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723571 | ||||||
chr10:68723581
|
A | G | 2 | a0001c0001t0001g0341a0001c0001t0001g0348 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.73+1004A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723581 | ||||||
chr10:68723584
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.73+1007C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723584 | ||||||
chr10:68723586
|
T | C | 2 | a0001c0001t0001g0341a0001c0001t0001g0348 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.73+1009T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723586 | ||||||
chr10:68723624
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.73+1047A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723624 | ||||||
chr10:68723658
|
C | T | 3 | a0001c0003t0001g0337a0001c0003t0001g0338a0001c0003t0001g0339 | 3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73+1081C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723658 | ||||||
chr10:68723683
|
C | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.73+1106C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723683 | ||||||
chr10:68723704
|
C | T | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(306): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.73+1127C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723704 | ||||||
chr10:68723758
|
G | T | 1 | a0001c0001t0001g0336 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.73+1181G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723758 | ||||||
chr10:68723853
|
GA | G | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(318): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.73+1289delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723853 | |||||
chr10:68723867
|
G | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+1290G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723867 | ||||||
chr10:68723988
|
GTC | G | 4 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(1): Show | 4 | HG02165.hp1 NA18940.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.73+1415_73+1416del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723988 | |||||
chr10:68723990
|
C | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+1413C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723990 | ||||||
chr10:68724049
|
T | C | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.73+1472T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724049 | ||||||
chr10:68724061
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.73+1484A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724061 | ||||||
chr10:68724081
|
G | C | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.73+1504G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724081 | ||||||
chr10:68724151
|
T | C | 68 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(65): Show | 68 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(65): Show |
intron_variant | MODIFIER | c.73+1574T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724151 | ||||||
chr10:68724160
|
GA | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.73+1595delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68724160 | |||||
chr10:68724435
|
A | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.73+1858A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724435 | ||||||
chr10:68724609
|
T | C | 68 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(65): Show | 68 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(65): Show |
intron_variant | MODIFIER | c.73+2032T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724609 | ||||||
chr10:68724755
|
A | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.73+2178A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724755 | ||||||
chr10:68724832
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+2255A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724832 | ||||||
chr10:68724855
|
G | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.73+2278G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724855 | ||||||
chr10:68724988
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.73+2411G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724988 | ||||||
chr10:68724989
|
G | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.73+2412G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724989 | ||||||
chr10:68725099
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.73+2522G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725099 | ||||||
chr10:68725269
|
G | C | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.73+2692G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725269 | ||||||
chr10:68725292
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.73+2715C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725292 | ||||||
chr10:68725315
|
T | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+2738T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725315 | ||||||
chr10:68725320
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.73+2743C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725320 | ||||||
chr10:68725325
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.73+2748G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725325 | ||||||
chr10:68725397
|
C | CA | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73+2828dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68725397 | |||||
chr10:68725430
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.73+2853C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725430 | ||||||
chr10:68725744
|
C | T | 23 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(20): Show | 23 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.73+3167C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725744 | ||||||
chr10:68725755
|
T | G | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.73+3178T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725755 | ||||||
chr10:68725945
|
A | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+3368A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725945 | ||||||
chr10:68725954
|
A | C | 2 | a0001c0003t0004g0071a0001c0003t0004g0072 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.73+3377A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725954 | ||||||
chr10:68726113
|
T | TA | 16 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0167others(13): Show | 16 | HG00423.hp2 HG01361.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.73+3556dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68726113 | |||||
chr10:68726129
|
A | G | 1 | a0001c0002t0001g0110 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.73+3552A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726129 | ||||||
chr10:68726130
|
A | G | 1 | a0001c0003t0004g0070 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73+3553A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726130 | ||||||
chr10:68726157
|
A | AT | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.73+3592dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68726157 | |||||
chr10:68726211
|
G | T | 1 | a0001c0002t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.73+3634G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726211 | ||||||
chr10:68726216
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.73+3639A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726216 | ||||||
chr10:68726456
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.73+3879C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726456 | ||||||
chr10:68726558
|
A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73+3981A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726558 | ||||||
chr10:68726568
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.73+3991T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726568 | ||||||
chr10:68726593
|
A | G | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.73+4016A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726593 | ||||||
chr10:68726687
|
CAT | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG02056.hp2 NA19007.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.73+4112_73+4113del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68726687 | |||||
chr10:68726786
|
A | C | 9 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(6): Show | 9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.73+4209A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726786 | ||||||
chr10:68726793
|
C | A | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.73+4216C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726793 | ||||||
chr10:68726825
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.73+4248G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726825 | ||||||
chr10:68726846
|
A | G | 1 | a0001c0001t0003g0041 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.73+4269A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726846 | ||||||
chr10:68726853
|
G | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+4276G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726853 | ||||||
chr10:68726853
|
G | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+4276G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726853 | ||||||
chr10:68727062
|
A | AT | 6 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+4496dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68727062 | |||||
chr10:68727073
|
T | G | 2 | a0001c0001t0001g0175a0001c0001t0010g0353 | 2 | HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.73+4496T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727073 | ||||||
chr10:68727074
|
G | GT | 53 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0037others(50): Show | 54 | HG00621.hp1 HG01106.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.73+4510dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68727074 | |||||
chr10:68727074
|
G | T | 2 | a0001c0001t0001g0334a0001c0001t0010g0353 | 2 | HG02074.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.73+4497G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727074 | ||||||
chr10:68727131
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.73+4554G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727131 | ||||||
chr10:68727147
|
A | G | 3 | a0001c0003t0002g0061a0001c0003t0002g0062a0001c0003t0002g0063 | 3 | HG03130.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.73+4570A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727147 | ||||||
chr10:68727231
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.73+4654C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727231 | ||||||
chr10:68727355
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.73+4778A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727355 | ||||||
chr10:68727396
|
A | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+4819A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727396 | ||||||
chr10:68727506
|
G | A | 38 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0003t0002g0047others(35): Show | 38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.73+4929G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727506 | ||||||
chr10:68727605
|
C | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.73+5028C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727605 | ||||||
chr10:68727650
|
A | G | 2 | a0001c0001t0001g0329a0001c0001t0001g0333 | 2 | HG00741.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.73+5073A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727650 | ||||||
chr10:68727754
|
A | G | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.73+5177A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727754 | ||||||
chr10:68727833
|
A | G | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+5256A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727833 | ||||||
chr10:68727997
|
C | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG00099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.73+5420C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727997 | ||||||
chr10:68728024
|
A | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+5447A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728024 | ||||||
chr10:68728042
|
G | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0241a0001c0001t0001g0242others(4): Show | 7 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+5465G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728042 | ||||||
chr10:68728184
|
A | G | 1 | a0001c0001t0005g0240 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.73+5607A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728184 | ||||||
chr10:68728214
|
T | A | 9 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(6): Show | 9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.73+5637T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728214 | ||||||
chr10:68728300
|
AT | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(36): Show | 40 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.73+5735delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68728300 | |||||
chr10:68728360
|
T | G | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+5783T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728360 | ||||||
chr10:68728471
|
G | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+5894G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728471 | ||||||
chr10:68728540
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.73+5963G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728540 | ||||||
chr10:68728603
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.73+6026A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728603 | ||||||
chr10:68728682
|
C | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.73+6105C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728682 | ||||||
chr10:68728866
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.73+6289A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728866 | ||||||
chr10:68728982
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.73+6405G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728982 | ||||||
chr10:68729057
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.73+6480A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729057 | ||||||
chr10:68729235
|
G | T | 2 | a0001c0003t0002g0061a0001c0003t0002g0063 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.73+6658G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729235 | ||||||
chr10:68729274
|
G | GT | 16 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0042others(13): Show | 16 | HG00735.hp2 HG02293.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.73+6710dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729274 | |||||
chr10:68729414
|
C | T | 6 | a0001c0003t0004g0067a0001c0003t0004g0068a0001c0003t0004g0070others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+6837C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729414 | ||||||
chr10:68729430
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.73+6853C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729430 | ||||||
chr10:68729610
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.73+7033C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729610 | ||||||
chr10:68729702
|
TA | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.73+7141delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729702 | |||||
chr10:68729702
|
TAA | T | 8 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0004t0001g0271others(5): Show | 8 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.73+7140_73+7141del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729702 | |||||
chr10:68729784
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-7092A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729784 | ||||||
chr10:68729820
|
G | A | 4 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0287others(1): Show | 4 | HG02074.hp2 HG02083.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-7056G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729820 | ||||||
chr10:68729889
|
G | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-6987G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729889 | ||||||
chr10:68729922
|
CT | C | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.74-6943delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729922 | |||||
chr10:68729925
|
T | C | 16 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(13): Show | 16 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.74-6951T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729925 | ||||||
chr10:68730047
|
G | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-6829G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730047 | ||||||
chr10:68730199
|
C | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-6677C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730199 | ||||||
chr10:68730262
|
G | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-6614G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730262 | ||||||
chr10:68730281
|
A | T | 1 | a0001c0002t0001g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.74-6595A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730281 | ||||||
chr10:68730326
|
A | AAT | 16 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0177others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.74-6531_74-6530dup others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68730326 | |||||
chr10:68730326
|
A | AATATAT | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.74-6535_74-6530dup others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68730326 | |||||
chr10:68730343
|
A | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.74-6533A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730343 | ||||||
chr10:68730347
|
T | A | 1 | a0001c0002t0001g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.74-6529T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730347 | ||||||
chr10:68730349
|
A | T | 54 | a0001c0002t0001g0006a0001c0002t0001g0109a0001c0002t0001g0110others(51): Show | 54 | HG00544.hp1 HG02040.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.74-6527A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730349 | ||||||
chr10:68730414
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.74-6462T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730414 | ||||||
chr10:68730578
|
T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-6298T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730578 | ||||||
chr10:68730594
|
C | T | 2 | a0001c0002t0001g0148a0001c0002t0001g0149 | 2 | NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.74-6282C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730594 | ||||||
chr10:68730692
|
T | G | 3 | a0001c0003t0001g0337a0001c0003t0001g0338a0001c0003t0001g0339 | 3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.74-6184T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730692 | ||||||
chr10:68730766
|
C | T | 2 | a0001c0002t0001g0148a0001c0002t0001g0149 | 2 | NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.74-6110C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730766 | ||||||
chr10:68730772
|
C | T | 54 | a0001c0002t0001g0006a0001c0002t0001g0109a0001c0002t0001g0110others(51): Show | 54 | HG00544.hp1 HG02040.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.74-6104C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730772 | ||||||
chr10:68730929
|
G | A | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.74-5947G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730929 | ||||||
chr10:68731074
|
GTATC | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-5798_74-5795del others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731074 | |||||
chr10:68731258
|
T | A | 1 | a0001c0002t0001g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.74-5618T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731258 | ||||||
chr10:68731286
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-5590C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731286 | ||||||
chr10:68731354
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-5522C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731354 | ||||||
chr10:68731425
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.74-5451C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731425 | ||||||
chr10:68731430
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.74-5446A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731430 | ||||||
chr10:68731509
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.74-5367C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731509 | ||||||
chr10:68731511
|
C | G | 3 | a0001c0003t0001g0337a0001c0003t0001g0338a0001c0003t0001g0339 | 3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.74-5365C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731511 | ||||||
chr10:68731559
|
A | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-5317A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731559 | ||||||
chr10:68731591
|
G | GT | 50 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(47): Show | 50 | HG00544.hp1 HG01123.hp2 HG01256.hp1 others(47): Show |
intron_variant | MODIFIER | c.74-5261dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | |||||
chr10:68731591
|
G | GTT | 10 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 11 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.74-5262_74-5261dup others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | |||||
chr10:68731591
|
GT | G | 59 | a0001c0001t0001g0011a0001c0001t0001g0164a0001c0001t0001g0173others(56): Show | 59 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.74-5261delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | |||||
chr10:68731591
|
GTT | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(164): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.74-5262_74-5261del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | |||||
chr10:68731602
|
T | G | 1 | a0001c0001t0001g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.74-5274T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731602 | ||||||
chr10:68731683
|
C | T | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.74-5193C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731683 | ||||||
chr10:68731731
|
C | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-5145C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731731 | ||||||
chr10:68732181
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 94 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.74-4695T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732181 | ||||||
chr10:68732190
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0237 | 2 | HG00735.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.74-4686C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732190 | ||||||
chr10:68732312
|
A | G | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-4564A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732312 | ||||||
chr10:68732336
|
T | TTTTG | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(10): Show | 13 | HG01109.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.74-4511_74-4508dup others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68732336 | |||||
chr10:68732336
|
TTTTG | T | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-4511_74-4508del others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68732336 | |||||
chr10:68732348
|
G | T | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.74-4528G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732348 | ||||||
chr10:68732470
|
C | T | 2 | a0001c0003t0002g0057a0001c0003t0017g0046 | 2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.74-4406C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732470 | ||||||
chr10:68732543
|
T | C | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4333T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732543 | ||||||
chr10:68732545
|
C | T | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4331C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732545 | ||||||
chr10:68732546
|
A | G | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4330A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732546 | ||||||
chr10:68732548
|
C | T | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4328C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732548 | ||||||
chr10:68732549
|
G | A | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4327G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732549 | ||||||
chr10:68732551
|
G | A | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4325G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732551 | ||||||
chr10:68732555
|
G | C | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4321G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732555 | ||||||
chr10:68732595
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-4281C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732595 | ||||||
chr10:68732987
|
G | T | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.74-3889G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732987 | ||||||
chr10:68733009
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.74-3867A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733009 | ||||||
chr10:68733057
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.74-3819G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733057 | ||||||
chr10:68733058
|
G | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.74-3818G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733058 | ||||||
chr10:68733125
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.74-3751A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733125 | ||||||
chr10:68733207
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.74-3669C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733207 | ||||||
chr10:68733282
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(40): Show | 44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.74-3594G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733282 | ||||||
chr10:68733286
|
C | T | 5 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.74-3590C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733286 | ||||||
chr10:68733366
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.74-3510C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733366 | ||||||
chr10:68733374
|
G | C | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.74-3502G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733374 | ||||||
chr10:68733495
|
CA | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.74-3380delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733495 | ||||||
chr10:68733532
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-3344C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733532 | ||||||
chr10:68733533
|
T | C | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0003t0001g0337others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-3343T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733533 | ||||||
chr10:68733640
|
T | C | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.74-3236T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733640 | ||||||
chr10:68733780
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.74-3096C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733780 | ||||||
chr10:68733789
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.74-3087G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733789 | ||||||
chr10:68733877
|
T | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.74-2999T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733877 | ||||||
chr10:68734030
|
A | G | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG00558.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.74-2846A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734030 | ||||||
chr10:68734079
|
T | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.74-2797T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734079 | ||||||
chr10:68734115
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-2761G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734115 | ||||||
chr10:68734488
|
C | T | 3 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0056 | 3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.74-2388C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734488 | ||||||
chr10:68735109
|
A | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-1767A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735109 | ||||||
chr10:68735158
|
G | A | 1 | a0002c0005t0008g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.74-1718G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735158 | ||||||
chr10:68735240
|
C | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.74-1636C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735240 | ||||||
chr10:68735287
|
G | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-1589G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735287 | ||||||
chr10:68735371
|
C | CT | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.74-1485dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68735371 | |||||
chr10:68735371
|
C | CTT | 41 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.74-1486_74-1485dup others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68735371 | |||||
chr10:68735371
|
C | CTTT | 22 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0003t0002g0047others(19): Show | 22 | HG00639.hp2 HG01081.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.74-1487_74-1485dup others(3): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68735371 | |||||
chr10:68735395
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-1481A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735395 | ||||||
chr10:68735402
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-1474G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735402 | ||||||
chr10:68735420
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.74-1456G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735420 | ||||||
chr10:68735433
|
A | G | 12 | a0001c0003t0002g0061a0001c0003t0002g0062a0001c0003t0002g0063others(9): Show | 12 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-1443A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735433 | ||||||
chr10:68735604
|
C | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-1272C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735604 | ||||||
chr10:68735652
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.74-1224T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735652 | ||||||
chr10:68735787
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.74-1089T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735787 | ||||||
chr10:68735789
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0100 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.74-1087A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735789 | ||||||
chr10:68735852
|
A | G | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.74-1024A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735852 | ||||||
chr10:68735897
|
G | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.74-979G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735897 | ||||||
chr10:68735955
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.74-921T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735955 | ||||||
chr10:68736041
|
T | C | 39 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.74-835T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736041 | ||||||
chr10:68736260
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.74-616A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736260 | ||||||
chr10:68736335
|
T | TACC | 9 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(6): Show | 9 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.74-540_74-539insCC others(1): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68736335 | |||||
chr10:68736335
|
T | TATC | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(336): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.74-540_74-538dupAT others(1): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68736335 | |||||
chr10:68736518
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.74-358A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736518 | ||||||
chr10:68736546
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.74-330T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736546 | ||||||
chr10:68736557
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0216 | 3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.74-319C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736557 | ||||||
chr10:68737210
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+162G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737210 | ||||||
chr10:68737285
|
G | C | 2 | a0001c0004t0006g0268a0001c0004t0006g0269 | 2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+237G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737285 | ||||||
chr10:68737326
|
G | C | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.246+278G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737326 | ||||||
chr10:68737462
|
C | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.247-383C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737462 | ||||||
chr10:68737498
|
C | CA | 11 | a0001c0001t0001g0034a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 11 | HG01109.hp1 HG02145.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-327dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr10 | 68737498 | |||||
chr10:68737498
|
CA | C | 11 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0273others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-327delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr10 | 68737498 | |||||
chr10:68737498
|
CAA | C | 35 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.247-328_247-327del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr10 | 68737498 | |||||
chr10:68737563
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.247-282C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737563 | ||||||
chr10:68737569
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.247-276C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737569 | ||||||
chr10:68737600
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.247-245T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737600 | ||||||
chr10:68737653
|
A | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.247-192A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737653 | ||||||
chr10:68737725
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.247-120A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737725 | ||||||
chr10:68737931
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.291+42G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68737931 | ||||||
chr10:68737975
|
C | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+86C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68737975 | ||||||
chr10:68737998
|
A | G | 1 | a0001c0001t0001g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.291+109A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68737998 | ||||||
chr10:68738042
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.291+153C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738042 | ||||||
chr10:68738141
|
G | A | 2 | a0001c0001t0001g0291a0003c0006t0001g0290 | 2 | HG01074.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.291+252G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738141 | ||||||
chr10:68738283
|
G | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.291+394G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738283 | ||||||
chr10:68738322
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.291+433G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738322 | ||||||
chr10:68738592
|
TTTTATTT others(7): Show |
T | 1 | a0001c0001t0001g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291+714_291+727del others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr10 | 68738592 | |||||
chr10:68738596
|
A | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0312 | 3 | HG02886.hp2 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.291+707A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738596 | ||||||
chr10:68738596
|
AT | A | 6 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0229others(3): Show | 6 | HG01069.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+716delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr10 | 68738596 | |||||
chr10:68738698
|
C | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.291+809C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738698 | ||||||
chr10:68738775
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.291+886A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738775 | ||||||
chr10:68738791
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.291+902A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738791 | ||||||
chr10:68738822
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.291+933G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738822 | ||||||
chr10:68738897
|
A | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+1008A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738897 | ||||||
chr10:68738922
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.291+1033C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738922 | ||||||
chr10:68739257
|
C | A | 2 | a0001c0003t0002g0058a0001c0003t0002g0059 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.291+1368C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739257 | ||||||
chr10:68739269
|
C | T | 1 | a0001c0001t0005g0240 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.292-1360C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739269 | ||||||
chr10:68739460
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.292-1169T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739460 | ||||||
chr10:68739581
|
G | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.292-1048G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739581 | ||||||
chr10:68739655
|
C | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.292-974C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739655 | ||||||
chr10:68739655
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.292-974C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739655 | ||||||
chr10:68739667
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG01257.hp2 HG01952.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-962C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739667 | ||||||
chr10:68739782
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.292-847T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739782 | ||||||
chr10:68740047
|
A | G | 2 | a0001c0002t0001g0106a0001c0002t0001g0108 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.292-582A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68740047 | ||||||
chr10:68740170
|
G | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0105 | 2 | HG00140.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.292-459G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68740170 | ||||||
chr10:68740414
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292-215C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68740414 | ||||||
chr10:68740713
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324+52A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740713 | ||||||
chr10:68740739
|
C | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+78C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740739 | ||||||
chr10:68740820
|
A | G | 2 | a0001c0003t0002g0058a0001c0003t0002g0059 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.324+159A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740820 | ||||||
chr10:68740871
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.324+210T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740871 | ||||||
chr10:68740883
|
T | TTTTA | 10 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0178others(7): Show | 10 | HG00621.hp1 HG01123.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+266_324+269dup others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | |||||
chr10:68740883
|
TTTTA | T | 37 | a0001c0001t0001g0027a0001c0001t0001g0081a0001c0001t0001g0089others(34): Show | 37 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.324+266_324+269del others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | |||||
chr10:68740883
|
TTTTATTT others(1): Show |
T | 8 | a0001c0001t0001g0033a0001c0001t0001g0175a0001c0001t0001g0205others(5): Show | 8 | HG00741.hp1 HG01361.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+262_324+269del others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | |||||
chr10:68740883
|
TTTTATTT others(5): Show |
T | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG01257.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+258_324+269del others(12): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | |||||
chr10:68740883
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324+254_324+269del others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | |||||
chr10:68740884
|
TTTATTTA others(8): Show |
T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.324+226_324+240del others(15): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740884 | |||||
chr10:68740887
|
A | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0170 | 2 | HG01517.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.324+226A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740887 | ||||||
chr10:68740953
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.324+292A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740953 | ||||||
chr10:68741066
|
A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.324+405A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741066 | ||||||
chr10:68741141
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+480G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741141 | ||||||
chr10:68741145
|
A | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324+484A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741145 | ||||||
chr10:68741149
|
C | G | 1 | a0001c0002t0001g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.324+488C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741149 | ||||||
chr10:68741298
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324+637G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741298 | ||||||
chr10:68741392
|
C | T | 2 | a0001c0004t0001g0271a0001c0004t0001g0272 | 2 | HG03491.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.324+731C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741392 | ||||||
chr10:68741464
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0237 | 2 | HG00735.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.324+803G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741464 | ||||||
chr10:68741520
|
T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.325-856T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741520 | ||||||
chr10:68741521
|
G | A | 1 | a0001c0007t0001g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.325-855G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741521 | ||||||
chr10:68741559
|
G | A | 2 | a0001c0003t0004g0071a0001c0003t0004g0072 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.325-817G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741559 | ||||||
chr10:68741591
|
C | A | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.325-785C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741591 | ||||||
chr10:68741670
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-706T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741670 | ||||||
chr10:68741936
|
A | G | 1 | a0001c0002t0001g0136 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.325-440A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741936 | ||||||
chr10:68742153
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.325-223G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68742153 | ||||||
chr10:68742170
|
G | C | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0003t0001g0337others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-206G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68742170 | ||||||
chr10:68742646
|
A | G | 1 | a0001c0001t0001g0230 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.518+77A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68742646 | ||||||
chr10:68742669
|
T | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.518+100T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68742669 | ||||||
chr10:68742851
|
C | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+282C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68742851 | ||||||
chr10:68742909
|
C | T | 1 | a0001c0001t0009g0013 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.518+340C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68742909 | ||||||
chr10:68743035
|
T | C | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.518+466T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743035 | ||||||
chr10:68743036
|
G | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+467G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743036 | ||||||
chr10:68743082
|
G | A | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.518+513G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743082 | ||||||
chr10:68743200
|
CTTT | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+643_518+645del others(3): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743200 | |||||
chr10:68743223
|
G | A | 1 | a0001c0003t0004g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.518+654G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743223 | ||||||
chr10:68743393
|
C | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+824C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743393 | ||||||
chr10:68743421
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.518+852C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743421 | ||||||
chr10:68743703
|
C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.518+1134C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743703 | ||||||
chr10:68743724
|
ATTTG | A | 64 | a0001c0001t0001g0089a0001c0002t0001g0006a0001c0002t0001g0091others(61): Show | 64 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(61): Show |
intron_variant | MODIFIER | c.518+1163_518+1166d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743724 | |||||
chr10:68743728
|
GTTTGTTT others(1): Show |
G | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(69): Show | 73 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.518+1163_518+1170d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743728 | |||||
chr10:68743728
|
GTTTGTTT others(5): Show |
G | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.518+1163_518+1174d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743728 | |||||
chr10:68743732
|
G | A | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.518+1163G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743732 | ||||||
chr10:68743732
|
GTTTA | G | 9 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(6): Show | 9 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.518+1192_518+1195d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743732 | |||||
chr10:68743767
|
T | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+1198T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743767 | ||||||
chr10:68743773
|
CAG | C | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.518+1207_518+1208d others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743773 | |||||
chr10:68744029
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0011 | 2 | HG01257.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.518+1460G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744029 | ||||||
chr10:68744085
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.518+1516A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744085 | ||||||
chr10:68744125
|
T | C | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0003t0001g0337others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+1556T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744125 | ||||||
chr10:68744181
|
A | G | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.518+1612A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744181 | ||||||
chr10:68744234
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0238 | 2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.518+1665A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744234 | ||||||
chr10:68744303
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.518+1734C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744303 | ||||||
chr10:68744420
|
T | A | 14 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(11): Show | 14 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.518+1851T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744420 | ||||||
chr10:68744505
|
G | A | 39 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.518+1936G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744505 | ||||||
chr10:68744522
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.518+1953A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744522 | ||||||
chr10:68744620
|
G | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+2051G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744620 | ||||||
chr10:68744709
|
T | C | 5 | a0001c0002t0001g0109a0001c0002t0001g0126a0001c0002t0001g0140others(2): Show | 5 | NA18946.hp1 NA18960.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+2140T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744709 | ||||||
chr10:68744833
|
CT | C | 6 | a0001c0001t0001g0180a0001c0001t0001g0210a0001c0001t0001g0317others(3): Show | 6 | HG01168.hp2 NA18941.hp2 NA19060.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+2278delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68744833 | |||||
chr10:68744916
|
T | G | 3 | a0001c0003t0001g0337a0001c0003t0001g0338a0001c0003t0001g0339 | 3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.519-2245T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744916 | ||||||
chr10:68744996
|
AAATT | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.519-2148_519-2145d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68744996 | |||||
chr10:68745074
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.519-2087T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745074 | ||||||
chr10:68745075
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.519-2086G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745075 | ||||||
chr10:68745092
|
G | A | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.519-2069G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745092 | ||||||
chr10:68745167
|
G | A | 1 | a0001c0002t0001g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.519-1994G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745167 | ||||||
chr10:68745227
|
C | T | 1 | a0001c0002t0001g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.519-1934C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745227 | ||||||
chr10:68745325
|
A | G | 4 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0203others(1): Show | 4 | NA18984.hp1 NA18990.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-1836A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745325 | ||||||
chr10:68745458
|
C | T | 5 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0002t0001g0106others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-1703C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745458 | ||||||
chr10:68745465
|
C | CT | 36 | a0001c0002t0001g0113a0001c0003t0002g0047a0001c0003t0002g0048others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.519-1682dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68745465 | |||||
chr10:68745487
|
G | A | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.519-1674G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745487 | ||||||
chr10:68745513
|
G | C | 1 | a0001c0001t0001g0258 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.519-1648G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745513 | ||||||
chr10:68745519
|
A | C | 1 | a0001c0002t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.519-1642A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745519 | ||||||
chr10:68745556
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.519-1605C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745556 | ||||||
chr10:68745620
|
C | T | 7 | a0001c0003t0002g0066a0001c0003t0004g0067a0001c0003t0004g0068others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.519-1541C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745620 | ||||||
chr10:68745646
|
T | C | 2 | a0001c0003t0002g0058a0001c0003t0002g0059 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.519-1515T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745646 | ||||||
chr10:68745743
|
C | T | 3 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0322 | 3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.519-1418C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745743 | ||||||
chr10:68745847
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0009g0013 | 3 | HG01069.hp1 HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.519-1314A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745847 | ||||||
chr10:68745908
|
G | A | 1 | a0001c0004t0006g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.519-1253G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745908 | ||||||
chr10:68745970
|
T | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG00544.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-1191T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745970 | ||||||
chr10:68745974
|
A | G | 12 | a0001c0003t0002g0061a0001c0003t0002g0062a0001c0003t0002g0063others(9): Show | 12 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.519-1187A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745974 | ||||||
chr10:68746050
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.519-1111A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746050 | ||||||
chr10:68746065
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519-1096C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746065 | ||||||
chr10:68746139
|
ATTTTTGT others(6): Show |
A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.519-1021_519-1009d others(15): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746139 | ||||||
chr10:68746232
|
A | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.519-929A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746232 | ||||||
chr10:68746262
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.519-899C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746262 | ||||||
chr10:68746333
|
G | A | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.519-828G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746333 | ||||||
chr10:68746371
|
G | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519-790G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746371 | ||||||
chr10:68746384
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.519-777C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746384 | ||||||
chr10:68746491
|
A | C | 1 | a0001c0003t0002g0055 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.519-670A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746491 | ||||||
chr10:68746509
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.519-652A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746509 | ||||||
chr10:68746617
|
C | T | 1 | a0001c0001t0001g0230 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.519-544C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746617 | ||||||
chr10:68746882
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.519-279C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746882 | ||||||
chr10:68746890
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.519-271T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746890 | ||||||
chr10:68747103
|
G | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519-58G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68747103 | ||||||
chr10:68747145
|
C | CT | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(36): Show | 40 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
splice_region_variant&intron_variant | LOW | c.519-5dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68747145 | |||||
chr10:68747333
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.634-41A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 7/24 | chr10 | 68747333 | ||||||
chr10:68747339
|
A | AT | 15 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0172others(12): Show | 16 | HG02056.hp2 NA18939.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.634-27dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr10 | 68747339 | |||||
chr10:68747695
|
A | G | 1 | a0001c0001t0001g0320 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.826+129A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747695 | ||||||
chr10:68747725
|
T | C | 1 | a0001c0003t0002g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.826+159T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747725 | ||||||
chr10:68747747
|
A | T | 1 | a0001c0003t0002g0080 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.826+181A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747747 | ||||||
chr10:68747869
|
A | T | 1 | a0001c0003t0002g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826+303A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747869 | ||||||
chr10:68748140
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.826+574C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748140 | ||||||
chr10:68748218
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.826+652C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748218 | ||||||
chr10:68748261
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.826+695G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748261 | ||||||
chr10:68748485
|
C | CT | 25 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0098others(22): Show | 25 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.827-630dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr10 | 68748485 | |||||
chr10:68748525
|
A | G | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.827-611A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748525 | ||||||
chr10:68748639
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.827-497G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748639 | ||||||
chr10:68748837
|
C | A | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.827-299C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748837 | ||||||
chr10:68748925
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.827-211A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748925 | ||||||
chr10:68748982
|
C | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.827-154C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748982 | ||||||
chr10:68749058
|
G | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.827-78G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68749058 | ||||||
chr10:68749117
|
T | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(40): Show | 44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.827-19T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68749117 | ||||||
chr10:68749357
|
A | C | 1 | a0001c0001t0001g0016 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.956+92A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 9/24 | chr10 | 68749357 | ||||||
chr10:68749384
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.956+119T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 9/24 | chr10 | 68749384 | ||||||
chr10:68749723
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1118+38A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749723 | ||||||
chr10:68749772
|
G | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+87G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749772 | ||||||
chr10:68749845
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+160A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749845 | ||||||
chr10:68749880
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1118+195C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749880 | ||||||
chr10:68749914
|
AT | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031 | 3 | HG01934.hp1 NA18948.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1118+231delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68749914 | |||||
chr10:68749936
|
C | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0216 | 3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1118+251C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749936 | ||||||
chr10:68749995
|
G | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1118+310G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749995 | ||||||
chr10:68750021
|
T | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+336T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750021 | ||||||
chr10:68750207
|
CTTTTTTC others(1): Show |
C | 7 | a0001c0001t0001g0239a0001c0001t0001g0273a0001c0001t0001g0274others(4): Show | 7 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1118+529_1118+536d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750207 | |||||
chr10:68750207
|
CTTTTTTC others(2): Show |
C | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1118+529_1118+537d others(11): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750207 | |||||
chr10:68750207
|
CTTTTTTC others(3): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1118+529_1118+538d others(12): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750207 | |||||
chr10:68750214
|
CT | C | 8 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0002t0001g0126others(5): Show | 8 | HG00639.hp1 HG01106.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1118+548delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750214 | |||||
chr10:68750214
|
CTT | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(76): Show | 80 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(77): Show |
intron_variant | MODIFIER | c.1118+547_1118+548d others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750214 | |||||
chr10:68750220
|
T | G | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1118+535T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750220 | ||||||
chr10:68750237
|
A | G | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1118+552A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750237 | ||||||
chr10:68750267
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1118+582G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750267 | ||||||
chr10:68750276
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1118+591C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750276 | ||||||
chr10:68750410
|
C | T | 3 | a0001c0003t0002g0078a0001c0003t0002g0079a0001c0003t0002g0080 | 3 | NA18947.hp1 NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1118+725C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750410 | ||||||
chr10:68750455
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1118+770C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750455 | ||||||
chr10:68750780
|
A | G | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1118+1095A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750780 | ||||||
chr10:68750864
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1118+1179C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750864 | ||||||
chr10:68751021
|
T | G | 3 | a0001c0001t0001g0328a0001c0001t0007g0350a0001c0001t0007g0351 | 3 | HG02280.hp1 HG02559.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1118+1336T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751021 | ||||||
chr10:68751027
|
G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+1342G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751027 | ||||||
chr10:68751028
|
T | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+1343T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751028 | ||||||
chr10:68751033
|
G | GT | 19 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(16): Show | 19 | HG01081.hp1 HG01109.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1118+1359dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68751033 | |||||
chr10:68751033
|
G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+1348G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751033 | ||||||
chr10:68751057
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1118+1372C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751057 | ||||||
chr10:68751153
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1118+1468G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751153 | ||||||
chr10:68751153
|
G | C | 1 | a0001c0003t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1118+1468G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751153 | ||||||
chr10:68751297
|
G | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0241a0001c0001t0001g0242others(4): Show | 7 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1118+1612G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751297 | ||||||
chr10:68751446
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1118+1761C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751446 | ||||||
chr10:68751673
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1118+1988G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751673 | ||||||
chr10:68751724
|
C | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+2039C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751724 | ||||||
chr10:68751750
|
G | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+2065G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751750 | ||||||
chr10:68751796
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1119-2056A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751796 | ||||||
chr10:68751841
|
G | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0183a0001c0001t0001g0246others(1): Show | 4 | HG00280.hp1 HG01261.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119-2011G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751841 | ||||||
chr10:68751892
|
C | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1119-1960C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751892 | ||||||
chr10:68751920
|
G | GT | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(75): Show | 79 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.1119-1918dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68751920 | |||||
chr10:68751925
|
T | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1119-1927T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751925 | ||||||
chr10:68751925
|
T | TG | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG01346.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119-1927_1119-192 others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751925 | ||||||
chr10:68751955
|
C | T | 1 | a0001c0003t0004g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1119-1897C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751955 | ||||||
chr10:68751956
|
G | A | 1 | a0001c0003t0002g0051 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1119-1896G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751956 | ||||||
chr10:68752018
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0232 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1119-1834G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752018 | ||||||
chr10:68752042
|
G | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1119-1810G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752042 | ||||||
chr10:68752105
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031 | 3 | HG01934.hp1 NA18948.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1119-1747A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752105 | ||||||
chr10:68752119
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1119-1733C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752119 | ||||||
chr10:68752120
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-1732G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752120 | ||||||
chr10:68752169
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1119-1683C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752169 | ||||||
chr10:68752222
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-1630A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752222 | ||||||
chr10:68752259
|
A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1119-1593A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752259 | ||||||
chr10:68752366
|
C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-1486C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752366 | ||||||
chr10:68752610
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1119-1242G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752610 | ||||||
chr10:68752628
|
T | C | 1 | a0001c0004t0006g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1119-1224T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752628 | ||||||
chr10:68752673
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1119-1179C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752673 | ||||||
chr10:68752871
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1119-981T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752871 | ||||||
chr10:68752883
|
A | AATAG | 61 | a0001c0001t0001g0037a0001c0001t0001g0089a0001c0001t0001g0163others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1119-914_1119-911d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
A | AATAGATA others(1): Show |
14 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0228others(11): Show | 14 | HG00423.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1119-918_1119-911d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
A | AATAGATA others(5): Show |
4 | a0001c0001t0001g0313a0001c0001t0001g0326a0001c0003t0002g0075others(1): Show | 4 | HG02040.hp2 HG02647.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119-922_1119-911d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
A | AATAGATA others(9): Show |
1 | a0001c0001t0001g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1119-926_1119-911d others(18): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
AATAG | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(100): Show | 104 | HG00558.hp1 HG00642.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.1119-914_1119-911d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
AATAGATA others(1): Show |
A | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 76 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1119-918_1119-911d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
AATAGATA others(5): Show |
A | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(10): Show | 13 | HG01168.hp2 HG01243.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1119-922_1119-911d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
AATAGATA others(9): Show |
A | 8 | a0001c0001t0001g0005a0001c0001t0001g0085a0001c0001t0001g0168others(5): Show | 9 | HG01109.hp1 NA18939.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1119-926_1119-911d others(18): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752883
|
AATAGATA others(13): Show |
A | 2 | a0001c0001t0001g0172a0001c0001t0001g0325 | 2 | HG00280.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1119-930_1119-911d others(22): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | |||||
chr10:68752928
|
A | T | 1 | a0001c0001t0001g0308 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1119-924A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752928 | ||||||
chr10:68752938
|
A | T | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119-914A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752938 | ||||||
chr10:68752972
|
A | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1119-880A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752972 | ||||||
chr10:68752978
|
ATAGG | A | 3 | a0001c0003t0001g0337a0001c0003t0001g0338a0001c0003t0001g0339 | 3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1119-869_1119-866d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752978 | |||||
chr10:68753094
|
T | TTAGTTGT others(17): Show |
280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1119-747_1119-746i others(26): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68753094 | |||||
chr10:68753353
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1119-499G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753353 | ||||||
chr10:68753383
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-469G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753383 | ||||||
chr10:68753460
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.1119-392G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753460 | ||||||
chr10:68753472
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0231 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1119-380T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753472 | ||||||
chr10:68753669
|
G | A | 1 | a0001c0002t0001g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1119-183G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753669 | ||||||
chr10:68754163
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1344+86G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754163 | ||||||
chr10:68754180
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1344+103G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754180 | ||||||
chr10:68754188
|
G | C | 10 | a0001c0001t0001g0163a0001c0001t0001g0219a0001c0001t0001g0223others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+111G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754188 | ||||||
chr10:68754240
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1344+163T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754240 | ||||||
chr10:68754521
|
T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1345-193T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754521 | ||||||
chr10:68754564
|
T | A | 1 | a0001c0002t0001g0119 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1345-150T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754564 | ||||||
chr10:68754870
|
G | A | 1 | a0001c0001t0009g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1458+43G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 12/24 | chr10 | 68754870 | ||||||
chr10:68755133
|
T | C | 1 | a0001c0003t0014g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1459-237T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 12/24 | chr10 | 68755133 | ||||||
chr10:68755317
|
G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1459-53G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 12/24 | chr10 | 68755317 | ||||||
chr10:68755584
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1625+48A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 13/24 | chr10 | 68755584 | ||||||
chr10:68755671
|
A | G | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1625+135A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 13/24 | chr10 | 68755671 | ||||||
chr10:68756627
|
A | G | 1 | a0001c0003t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1836+144A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 14/24 | chr10 | 68756627 | ||||||
chr10:68756987
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(74): Show | 78 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.1837-307A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 14/24 | chr10 | 68756987 | ||||||
chr10:68757532
|
A | G | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1920+155A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757532 | ||||||
chr10:68757628
|
T | C | 1 | a0001c0003t0002g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1920+251T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757628 | ||||||
chr10:68757706
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.1920+329G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757706 | ||||||
chr10:68757797
|
G | C | 1 | a0001c0003t0002g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1920+420G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757797 | ||||||
chr10:68757833
|
TAAG | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1920+460_1920+462d others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68757833 | |||||
chr10:68757845
|
A | T | 3 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0322 | 3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1920+468A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757845 | ||||||
chr10:68757880
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0216 | 3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1920+503A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757880 | ||||||
chr10:68757886
|
G | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG01257.hp2 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1920+509G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757886 | ||||||
chr10:68757901
|
C | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1920+524C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757901 | ||||||
chr10:68758227
|
G | C | 1 | a0001c0002t0001g0131 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1920+850G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758227 | ||||||
chr10:68758269
|
G | A | 1 | a0001c0002t0001g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1920+892G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758269 | ||||||
chr10:68758338
|
A | T | 2 | a0001c0001t0001g0033a0001c0001t0016g0028 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1920+961A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758338 | ||||||
chr10:68758384
|
T | A | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1920+1007T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758384 | ||||||
chr10:68758483
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0216 | 3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1920+1106A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758483 | ||||||
chr10:68758503
|
A | AGT | 107 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 108 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1920+1167_1920+116 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
A | AGTGT | 17 | a0001c0001t0001g0216a0001c0001t0001g0244a0001c0001t0001g0257others(14): Show | 17 | HG01123.hp1 HG01515.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.1920+1165_1920+116 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
A | AGTGTGT | 17 | a0001c0001t0001g0087a0001c0001t0018g0088a0001c0002t0001g0106others(14): Show | 17 | HG00544.hp1 HG02145.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1920+1163_1920+116 others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
A | AGTGTGTG others(3): Show |
1 | a0001c0002t0001g0108 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1920+1159_1920+116 others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
A | AGTGTGTG others(5): Show |
1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1920+1157_1920+116 others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
AGT | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0022others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1920+1167_1920+116 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
AGTGT | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(30): Show | 34 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1920+1165_1920+116 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
AGTGTGT | A | 18 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0089others(15): Show | 18 | HG01346.hp2 HG01891.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.1920+1163_1920+116 others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
AGTGTGTG others(1): Show |
A | 5 | a0001c0001t0001g0081a0001c0001t0001g0341a0001c0001t0001g0348others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1920+1161_1920+116 others(12): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1920+1157_1920+116 others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758503
|
AGTGTGTG others(7): Show |
A | 9 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(6): Show | 9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1920+1155_1920+116 others(18): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | |||||
chr10:68758546
|
A | G | 7 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0229others(4): Show | 7 | HG01496.hp1 HG01952.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1920+1169A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758546 | ||||||
chr10:68758555
|
A | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1920+1178A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758555 | ||||||
chr10:68758612
|
T | TGTGTATA others(23): Show |
4 | a0001c0002t0001g0110a0001c0002t0001g0122a0001c0002t0001g0151others(1): Show | 4 | NA18947.hp2 NA18961.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1920+1251_1920+125 others(34): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758612 | |||||
chr10:68758612
|
TGTGTATA others(25): Show |
T | 1 | a0001c0002t0001g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1920+1282_1920+131 others(36): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758612 | |||||
chr10:68758614
|
TGTATATA others(23): Show |
T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1920+1240_1920+126 others(34): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758614 | |||||
chr10:68758615
|
GTA | G | 92 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(89): Show | 92 | HG00544.hp1 HG00639.hp2 HG01081.hp1 others(89): Show |
intron_variant | MODIFIER | c.1920+1252_1920+125 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758615 | |||||
chr10:68758615
|
GTATA | G | 3 | a0001c0002t0001g0134a0001c0003t0002g0061a0001c0003t0002g0063 | 3 | HG03130.hp1 HG03669.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1920+1250_1920+125 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758615 | |||||
chr10:68758617
|
A | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1920+1240A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758617 | ||||||
chr10:68758629
|
ATGTATAT others(55): Show |
A | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1920+1254_1920+131 others(66): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758629 | |||||
chr10:68758647
|
GTA | G | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1920+1284_1920+128 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758647 | |||||
chr10:68758649
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0035 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1920+1272A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758649 | ||||||
chr10:68758659
|
ATATGTAT others(25): Show |
A | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1920+1284_1920+131 others(36): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758659 | |||||
chr10:68758661
|
ATGTATAT others(24): Show |
A | 10 | a0001c0001t0001g0163a0001c0001t0001g0219a0001c0001t0001g0223others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1920+1286_1920+131 others(35): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758661 | |||||
chr10:68758661
|
ATGTATAT others(25): Show |
A | 5 | a0001c0001t0001g0172a0001c0001t0001g0205a0001c0001t0001g0215others(2): Show | 5 | HG02280.hp1 HG02559.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1920+1286_1920+131 others(36): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758661 | |||||
chr10:68758691
|
T | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(65): Show | 69 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.1920+1314T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758691 | ||||||
chr10:68758709
|
G | GTCT | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1920+1334_1920+133 others(7): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758709 | |||||
chr10:68758813
|
C | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1920+1436C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758813 | ||||||
chr10:68758858
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1920+1481A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758858 | ||||||
chr10:68758957
|
C | A | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1920+1580C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758957 | ||||||
chr10:68759105
|
ACAACAAC | A | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1920+1738_1920+174 others(11): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68759105 | |||||
chr10:68759238
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1921-1769G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759238 | ||||||
chr10:68759321
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1921-1686G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759321 | ||||||
chr10:68759415
|
AAAAT | A | 38 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0003t0002g0047others(35): Show | 38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1921-1586_1921-158 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68759415 | |||||
chr10:68759457
|
A | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-1550A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759457 | ||||||
chr10:68759561
|
C | CA | 15 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0171others(12): Show | 15 | HG00280.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1921-1433dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68759561 | |||||
chr10:68759807
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1921-1200T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759807 | ||||||
chr10:68759815
|
T | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-1192T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759815 | ||||||
chr10:68759846
|
A | T | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1921-1161A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759846 | ||||||
chr10:68759923
|
C | G | 3 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0056 | 3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1921-1084C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759923 | ||||||
chr10:68759990
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1921-1017A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759990 | ||||||
chr10:68760106
|
ACAGGCAC others(4): Show |
A | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1921-898_1921-888d others(13): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760106 | |||||
chr10:68760169
|
A | T | 1 | a0001c0002t0001g0125 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1921-838A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760169 | ||||||
chr10:68760204
|
GAGTGCAG others(5): Show |
G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-799_1921-788d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760204 | |||||
chr10:68760235
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1921-772A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760235 | ||||||
chr10:68760382
|
G | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1921-625G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760382 | ||||||
chr10:68760475
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1921-532C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760475 | ||||||
chr10:68760528
|
A | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1921-479A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760528 | ||||||
chr10:68760665
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1921-342G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760665 | ||||||
chr10:68760714
|
A | G | 7 | a0001c0003t0002g0066a0001c0003t0004g0067a0001c0003t0004g0068others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1921-293A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760714 | ||||||
chr10:68760745
|
T | A | 61 | a0001c0002t0001g0006a0001c0002t0001g0091a0001c0002t0001g0092others(58): Show | 61 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(58): Show |
intron_variant | MODIFIER | c.1921-262T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760745 | ||||||
chr10:68760832
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1921-175C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760832 | ||||||
chr10:68760872
|
C | A | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1921-135C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760872 | ||||||
chr10:68760873
|
A | C | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1921-134A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760873 | ||||||
chr10:68760879
|
CA | C | 61 | a0001c0002t0001g0006a0001c0002t0001g0091a0001c0002t0001g0092others(58): Show | 61 | HG00140.hp2 HG00642.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.1921-114delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760879 | |||||
chr10:68760879
|
CAA | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(35): Show | 39 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1921-115_1921-114d others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760879 | |||||
chr10:68760879
|
CAAA | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1921-116_1921-114d others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760879 | |||||
chr10:68760883
|
A | C | 3 | a0001c0002t0001g0134a0001c0002t0001g0136a0001c0002t0001g0150 | 3 | HG00544.hp1 HG02040.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1921-124A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760883 | ||||||
chr10:68760884
|
A | C | 1 | a0001c0002t0001g0119 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1921-123A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760884 | ||||||
chr10:68760947
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1921-60G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760947 | ||||||
chr10:68760949
|
T | C | 13 | a0001c0002t0001g0109a0001c0002t0001g0116a0001c0002t0001g0126others(10): Show | 13 | NA18946.hp1 NA18960.hp1 NA18968.hp2 others(10): Show |
intron_variant | MODIFIER | c.1921-58T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760949 | ||||||
chr10:68760963
|
C | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-44C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760963 | ||||||
chr10:68761272
|
T | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2106+80T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761272 | ||||||
chr10:68761284
|
A | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2106+92A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761284 | ||||||
chr10:68761312
|
A | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2106+120A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761312 | ||||||
chr10:68761312
|
AATTT | A | 3 | a0001c0003t0002g0078a0001c0003t0002g0079a0001c0003t0002g0080 | 3 | NA18947.hp1 NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2106+129_2106+132d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68761312 | |||||
chr10:68761316
|
T | A | 1 | a0001c0002t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2106+124T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761316 | ||||||
chr10:68761367
|
A | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(40): Show | 44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.2106+175A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761367 | ||||||
chr10:68761375
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2106+183C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761375 | ||||||
chr10:68761400
|
A | G | 1 | a0001c0001t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2106+208A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761400 | ||||||
chr10:68761508
|
A | G | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2106+316A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761508 | ||||||
chr10:68761603
|
C | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+411C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761603 | ||||||
chr10:68761632
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2106+440C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761632 | ||||||
chr10:68761665
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0082a0001c0001t0001g0083others(4): Show | 7 | HG01109.hp1 HG01993.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2106+473C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761665 | ||||||
chr10:68761728
|
A | G | 1 | a0001c0002t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2106+536A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761728 | ||||||
chr10:68761787
|
A | G | 1 | a0001c0002t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2106+595A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761787 | ||||||
chr10:68761790
|
A | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2106+598A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761790 | ||||||
chr10:68761906
|
A | G | 39 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2106+714A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761906 | ||||||
chr10:68762051
|
C | T | 1 | a0001c0003t0002g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2106+859C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762051 | ||||||
chr10:68762099
|
G | C | 1 | a0001c0007t0001g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2106+907G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762099 | ||||||
chr10:68762111
|
C | T | 3 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0322 | 3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2106+919C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762111 | ||||||
chr10:68762144
|
A | G | 39 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2106+952A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762144 | ||||||
chr10:68762327
|
TA | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2106+1146delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68762327 | |||||
chr10:68762344
|
C | CA | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2106+1158dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68762344 | |||||
chr10:68762355
|
CA | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2106+1173delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68762355 | |||||
chr10:68762473
|
A | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2106+1281A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762473 | ||||||
chr10:68762619
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2106+1427T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762619 | ||||||
chr10:68762679
|
A | C | 2 | a0001c0003t0002g0058a0001c0003t0002g0059 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2106+1487A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762679 | ||||||
chr10:68762745
|
T | A | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2106+1553T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762745 | ||||||
chr10:68762748
|
A | T | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2106+1556A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762748 | ||||||
chr10:68762752
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0282 | 2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2106+1560T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762752 | ||||||
chr10:68762907
|
C | T | 1 | a0001c0001t0003g0045 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2106+1715C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762907 | ||||||
chr10:68762948
|
AG | A | 14 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(11): Show | 14 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2106+1757delG | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762948 | ||||||
chr10:68762990
|
A | G | 2 | a0001c0004t0006g0268a0001c0004t0006g0269 | 2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2106+1798A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762990 | ||||||
chr10:68763112
|
CT | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2106+1929delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68763112 | |||||
chr10:68763141
|
CTTTA | C | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+1953_2106+195 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68763141 | |||||
chr10:68763153
|
A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2106+1961A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763153 | ||||||
chr10:68763174
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2106+1982C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763174 | ||||||
chr10:68763304
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2106+2112C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763304 | ||||||
chr10:68763316
|
A | C | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+2124A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763316 | ||||||
chr10:68763443
|
G | A | 1 | a0001c0001t0009g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2106+2251G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763443 | ||||||
chr10:68763497
|
C | T | 1 | a0001c0002t0011g0146 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2106+2305C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763497 | ||||||
chr10:68763511
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2106+2319G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763511 | ||||||
chr10:68763573
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2107-2315G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763573 | ||||||
chr10:68763593
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(2): Show | 5 | HG01934.hp1 NA18747.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2107-2295G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763593 | ||||||
chr10:68763739
|
T | C | 1 | a0001c0002t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2107-2149T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763739 | ||||||
chr10:68763790
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2107-2098C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763790 | ||||||
chr10:68763989
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2107-1899T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763989 | ||||||
chr10:68764175
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2107-1713A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764175 | ||||||
chr10:68764230
|
A | T | 38 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0003t0002g0047others(35): Show | 38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.2107-1658A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764230 | ||||||
chr10:68764381
|
C | CA | 30 | a0001c0001t0001g0042a0001c0003t0002g0047a0001c0003t0002g0048others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2107-1492dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68764381 | |||||
chr10:68764381
|
C | CAA | 7 | a0001c0003t0002g0066a0001c0003t0004g0067a0001c0003t0004g0068others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2107-1493_2107-149 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68764381 | |||||
chr10:68764539
|
CA | C | 9 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(6): Show | 9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2107-1337delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68764539 | |||||
chr10:68764620
|
T | G | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2107-1268T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764620 | ||||||
chr10:68764719
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2107-1169A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764719 | ||||||
chr10:68764881
|
A | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2107-1007A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764881 | ||||||
chr10:68764914
|
T | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107-974T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764914 | ||||||
chr10:68764932
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2107-956A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764932 | ||||||
chr10:68765048
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2107-840T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765048 | ||||||
chr10:68765376
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2107-512C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765376 | ||||||
chr10:68765420
|
C | G | 1 | a0001c0001t0001g0325 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2107-468C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765420 | ||||||
chr10:68765665
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2107-223G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765665 | ||||||
chr10:68765679
|
A | T | 2 | a0001c0001t0001g0341a0001c0001t0001g0348 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2107-209A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765679 | ||||||
chr10:68765728
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2107-160C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765728 | ||||||
chr10:68765832
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2107-56A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765832 | ||||||
chr10:68765834
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2107-54G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765834 | ||||||
chr10:68766186
|
G | GT | 14 | a0001c0001t0001g0197a0001c0001t0018g0088a0001c0003t0002g0061others(11): Show | 14 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.2298+115dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68766186 | |||||
chr10:68766186
|
G | T | 62 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0002t0001g0006others(59): Show | 62 | HG00544.hp1 HG01106.hp2 HG02040.hp1 others(59): Show |
intron_variant | MODIFIER | c.2298+107G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766186 | ||||||
chr10:68766187
|
T | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2298+108T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766187 | ||||||
chr10:68766215
|
T | A | 1 | a0001c0001t0001g0300 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2298+136T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766215 | ||||||
chr10:68766217
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2298+138T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766217 | ||||||
chr10:68766563
|
A | C | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+484A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766563 | ||||||
chr10:68766612
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2298+533C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766612 | ||||||
chr10:68766652
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2298+573G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766652 | ||||||
chr10:68766775
|
T | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+696T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766775 | ||||||
chr10:68766839
|
A | C | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2298+760A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766839 | ||||||
chr10:68767005
|
T | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0172others(13): Show | 17 | HG02056.hp2 NA18939.hp1 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.2298+926T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767005 | ||||||
chr10:68767054
|
C | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2298+975C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767054 | ||||||
chr10:68767250
|
AT | A | 7 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0229others(4): Show | 7 | HG01069.hp2 HG01496.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2298+1177delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68767250 | |||||
chr10:68767308
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2298+1229C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767308 | ||||||
chr10:68767403
|
G | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+1324G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767403 | ||||||
chr10:68767413
|
A | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+1334A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767413 | ||||||
chr10:68767618
|
C | T | 1 | a0001c0001t0001g0343 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2298+1539C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767618 | ||||||
chr10:68767828
|
A | AT | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2298+1752dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68767828 | |||||
chr10:68767904
|
T | C | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2298+1825T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767904 | ||||||
chr10:68768075
|
T | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2298+1996T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768075 | ||||||
chr10:68768304
|
CT | C | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2298+2236delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68768304 | |||||
chr10:68768428
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2298+2349C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768428 | ||||||
chr10:68768533
|
C | T | 2 | a0001c0001t0001g0183a0001c0002t0001g0096 | 2 | HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2298+2454C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768533 | ||||||
chr10:68768577
|
C | T | 3 | a0001c0003t0001g0337a0001c0003t0001g0338a0001c0003t0001g0339 | 3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2298+2498C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768577 | ||||||
chr10:68768638
|
A | G | 9 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(6): Show | 9 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.2298+2559A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768638 | ||||||
chr10:68768734
|
C | T | 12 | a0001c0003t0002g0061a0001c0003t0002g0062a0001c0003t0002g0063others(9): Show | 12 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2299-2472C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768734 | ||||||
chr10:68768787
|
A | G | 9 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(6): Show | 9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2299-2419A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768787 | ||||||
chr10:68768919
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2299-2287A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768919 | ||||||
chr10:68768968
|
A | G | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2299-2238A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768968 | ||||||
chr10:68769218
|
C | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0282 | 2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2299-1988C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769218 | ||||||
chr10:68769253
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2299-1953C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769253 | ||||||
chr10:68769295
|
T | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2299-1911T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769295 | ||||||
chr10:68769367
|
T | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2299-1839T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769367 | ||||||
chr10:68769379
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2299-1827G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769379 | ||||||
chr10:68769502
|
C | A | 16 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(13): Show | 16 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2299-1704C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769502 | ||||||
chr10:68769519
|
C | G | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2299-1687C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769519 | ||||||
chr10:68769655
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2299-1551A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769655 | ||||||
chr10:68769667
|
C | T | 1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2299-1539C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769667 | ||||||
chr10:68769758
|
G | A | 15 | a0001c0001t0001g0293a0001c0003t0002g0047a0001c0003t0002g0048others(12): Show | 15 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.2299-1448G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769758 | ||||||
chr10:68769828
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2299-1378C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769828 | ||||||
chr10:68769940
|
C | CA | 30 | a0001c0001t0001g0100a0001c0001t0001g0169a0001c0001t0001g0196others(27): Show | 30 | HG00735.hp1 HG01109.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2299-1244dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68769940 | |||||
chr10:68769940
|
CA | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(52): Show | 55 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.2299-1244delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68769940 | |||||
chr10:68770068
|
G | A | 38 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0003t0002g0047others(35): Show | 38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.2299-1138G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770068 | ||||||
chr10:68770160
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2299-1046A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770160 | ||||||
chr10:68770206
|
A | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2299-1000A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770206 | ||||||
chr10:68770418
|
T | A | 1 | a0001c0003t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2299-788T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770418 | ||||||
chr10:68770423
|
G | C | 1 | a0001c0003t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2299-783G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770423 | ||||||
chr10:68770635
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2299-571C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770635 | ||||||
chr10:68770762
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2299-444A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770762 | ||||||
chr10:68770805
|
C | T | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2299-401C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770805 | ||||||
chr10:68770816
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2299-390G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770816 | ||||||
chr10:68770880
|
A | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2299-326A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770880 | ||||||
chr10:68770889
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2299-317G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770889 | ||||||
chr10:68770917
|
A | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2299-289A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770917 | ||||||
chr10:68770947
|
G | A | 2 | a0001c0002t0001g0106a0001c0002t0001g0108 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2299-259G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770947 | ||||||
chr10:68770994
|
C | T | 23 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(20): Show | 23 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.2299-212C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770994 | ||||||
chr10:68771064
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2299-142C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68771064 | ||||||
chr10:68771080
|
A | G | 1 | a0001c0003t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2299-126A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68771080 | ||||||
chr10:68771192
|
A | G | 1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2299-14A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68771192 | ||||||
chr10:68771460
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2538+15C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771460 | ||||||
chr10:68771642
|
A | G | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+197A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771642 | ||||||
chr10:68771643
|
C | T | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+198C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771643 | ||||||
chr10:68771644
|
A | C | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+199A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771644 | ||||||
chr10:68771645
|
T | A | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+200T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771645 | ||||||
chr10:68771826
|
T | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2538+381T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771826 | ||||||
chr10:68771835
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2538+390A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771835 | ||||||
chr10:68771852
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2538+407A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771852 | ||||||
chr10:68771866
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2538+421A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771866 | ||||||
chr10:68771887
|
G | GA | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2538+443dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr10 | 68771887 | |||||
chr10:68771897
|
T | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2538+452T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771897 | ||||||
chr10:68771923
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2538+478T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771923 | ||||||
chr10:68772308
|
C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2539-680C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772308 | ||||||
chr10:68772315
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2539-673T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772315 | ||||||
chr10:68772316
|
C | A | 1 | a0001c0001t0001g0188 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2539-672C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772316 | ||||||
chr10:68772724
|
C | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2539-264C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772724 | ||||||
chr10:68772757
|
C | CA | 8 | a0001c0001t0001g0197a0001c0001t0001g0306a0001c0001t0001g0309others(5): Show | 8 | HG01109.hp2 HG01192.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2539-218dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr10 | 68772757 | |||||
chr10:68772757
|
CA | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(71): Show | 74 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.2539-218delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr10 | 68772757 | |||||
chr10:68772915
|
A | C | 3 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0322 | 3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2539-73A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772915 | ||||||
chr10:68773170
|
C | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+71C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773170 | ||||||
chr10:68773200
|
T | G | 1 | a0001c0001t0001g0308 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2650+101T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773200 | ||||||
chr10:68773233
|
G | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2650+134G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773233 | ||||||
chr10:68773342
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0036others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650+243G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773342 | ||||||
chr10:68773416
|
A | T | 1 | a0001c0001t0001g0304 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2650+317A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773416 | ||||||
chr10:68773420
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2650+321T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773420 | ||||||
chr10:68773436
|
G | A | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2650+337G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773436 | ||||||
chr10:68773452
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2650+353A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773452 | ||||||
chr10:68773535
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0232 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2650+436G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773535 | ||||||
chr10:68773546
|
C | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0180 | 2 | NA18961.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2650+447C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773546 | ||||||
chr10:68773665
|
C | CA | 8 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0177others(5): Show | 8 | HG02886.hp2 HG03453.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2650+579dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68773665 | |||||
chr10:68773678
|
AT | A | 60 | a0001c0002t0001g0006a0001c0002t0001g0091a0001c0002t0001g0092others(57): Show | 60 | HG00544.hp1 HG02040.hp1 HG02055.hp2 others(57): Show |
intron_variant | MODIFIER | c.2650+580delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773678 | ||||||
chr10:68773707
|
C | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2650+608C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773707 | ||||||
chr10:68773822
|
C | G | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2650+723C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773822 | ||||||
chr10:68773884
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2650+785T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773884 | ||||||
chr10:68773887
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2650+788A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773887 | ||||||
chr10:68773895
|
T | G | 2 | a0001c0003t0002g0062a0001c0008t0001g0284 | 2 | HG02135.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2650+796T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773895 | ||||||
chr10:68773904
|
T | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+805T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773904 | ||||||
chr10:68774081
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2650+982G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774081 | ||||||
chr10:68774196
|
T | C | 1 | a0001c0002t0001g0152 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2650+1097T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774196 | ||||||
chr10:68774320
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0084 | 2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2650+1221C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774320 | ||||||
chr10:68774352
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.2650+1253T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774352 | ||||||
chr10:68774570
|
G | T | 1 | a0001c0003t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2650+1471G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774570 | ||||||
chr10:68774630
|
C | CA | 8 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0310others(5): Show | 8 | HG02145.hp1 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2650+1545dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68774630 | |||||
chr10:68774713
|
A | G | 1 | a0001c0001t0001g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2650+1614A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774713 | ||||||
chr10:68774922
|
T | A | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2650+1823T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774922 | ||||||
chr10:68774925
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2650+1826G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774925 | ||||||
chr10:68774954
|
T | G | 14 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(11): Show | 14 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2650+1855T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774954 | ||||||
chr10:68774987
|
A | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2650+1888A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774987 | ||||||
chr10:68775194
|
A | G | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2650+2095A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775194 | ||||||
chr10:68775497
|
CT | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2650+2415delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775497 | |||||
chr10:68775503
|
T | C | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2650+2404T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775503 | ||||||
chr10:68775508
|
T | G | 13 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG01106.hp2 HG01109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2650+2409T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775508 | ||||||
chr10:68775509
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2650+2410T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775509 | ||||||
chr10:68775511
|
T | G | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2650+2412T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775511 | ||||||
chr10:68775687
|
C | CT | 30 | a0001c0002t0001g0006a0001c0002t0001g0092a0001c0002t0001g0094others(27): Show | 30 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.2650+2615dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | |||||
chr10:68775687
|
C | CTT | 13 | a0001c0002t0001g0091a0001c0003t0002g0051a0001c0003t0002g0060others(10): Show | 13 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2650+2614_2650+261 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | |||||
chr10:68775687
|
CT | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(46): Show | 50 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.2650+2615delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | |||||
chr10:68775687
|
CTTT | C | 11 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0214others(8): Show | 11 | HG01106.hp1 HG01175.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+2613_2650+261 others(7): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | |||||
chr10:68775687
|
CTTTT | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2650+2612_2650+261 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | |||||
chr10:68775687
|
CTTTTT | C | 11 | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0001g0225others(8): Show | 11 | HG01261.hp1 HG01261.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+2611_2650+261 others(9): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | |||||
chr10:68775687
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0007t0001g0280 | 3 | HG02280.hp1 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2650+2604_2650+261 others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | |||||
chr10:68775907
|
G | T | 1 | a0001c0002t0001g0119 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2650+2808G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775907 | ||||||
chr10:68775970
|
T | C | 349 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(346): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.2650+2871T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775970 | ||||||
chr10:68776065
|
G | A | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2650+2966G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776065 | ||||||
chr10:68776141
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2650+3042A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776141 | ||||||
chr10:68776186
|
A | G | 23 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(20): Show | 23 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.2650+3087A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776186 | ||||||
chr10:68776235
|
TTTTTC | T | 11 | a0001c0001t0001g0163a0001c0001t0001g0219a0001c0001t0001g0223others(8): Show | 11 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+3156_2650+316 others(9): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776235 | |||||
chr10:68776235
|
TTTTTCTT others(3): Show |
T | 1 | a0001c0001t0001g0250 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2650+3151_2650+316 others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776235 | |||||
chr10:68776236
|
T | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+3137T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776236 | ||||||
chr10:68776255
|
C | CT | 8 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0003t0001g0337others(5): Show | 8 | HG01106.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2650+3168dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776255 | |||||
chr10:68776433
|
GCGGATGC others(9): Show |
G | 4 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 4 | NA18942.hp1 NA18956.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650+3336_2650+335 others(20): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776433 | |||||
chr10:68776435
|
G | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | HG01257.hp2 HG01934.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2650+3336G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776435 | ||||||
chr10:68776515
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2650+3416G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776515 | ||||||
chr10:68776562
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2650+3463G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776562 | ||||||
chr10:68776658
|
GTCC | G | 3 | a0001c0002t0001g0137a0001c0002t0001g0148a0001c0002t0001g0149 | 3 | NA18980.hp1 NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2650+3568_2650+357 others(7): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776658 | |||||
chr10:68776816
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+3717C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776816 | ||||||
chr10:68776817
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2650+3718T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776817 | ||||||
chr10:68776937
|
G | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2650+3838G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776937 | ||||||
chr10:68777060
|
C | G | 2 | a0002c0005t0008g0049a0002c0005t0008g0050 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2650+3961C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777060 | ||||||
chr10:68777158
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2650+4059G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777158 | ||||||
chr10:68777166
|
C | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+4067C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777166 | ||||||
chr10:68777176
|
C | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 93 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2650+4077C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777176 | ||||||
chr10:68777273
|
C | A | 1 | a0001c0003t0002g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2650+4174C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777273 | ||||||
chr10:68777435
|
C | T | 1 | a0001c0001t0001g0349 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2650+4336C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777435 | ||||||
chr10:68777544
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2650+4445C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777544 | ||||||
chr10:68777552
|
C | T | 3 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0056 | 3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2650+4453C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777552 | ||||||
chr10:68777683
|
C | CA | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(43): Show | 47 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.2650+4597dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68777683 | |||||
chr10:68777699
|
C | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2650+4600C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777699 | ||||||
chr10:68777789
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2650+4690G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777789 | ||||||
chr10:68777817
|
A | T | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+4718A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777817 | ||||||
chr10:68777837
|
T | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2650+4738T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777837 | ||||||
chr10:68777909
|
A | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+4810A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777909 | ||||||
chr10:68777943
|
G | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2650+4844G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777943 | ||||||
chr10:68778214
|
T | C | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+5115T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778214 | ||||||
chr10:68778310
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2650+5211G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778310 | ||||||
chr10:68778531
|
C | CT | 6 | a0001c0002t0001g0125a0001c0002t0001g0134a0001c0002t0001g0136others(3): Show | 6 | HG00544.hp1 HG02040.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.2650+5443dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68778531 | |||||
chr10:68778532
|
T | TA | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2650+5433_2650+543 others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778532 | ||||||
chr10:68778773
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0196others(10): Show | 14 | NA18939.hp1 NA18940.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.2650+5674A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778773 | ||||||
chr10:68778820
|
C | T | 1 | a0001c0001t0001g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2650+5721C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778820 | ||||||
chr10:68778874
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0081others(1): Show | 4 | HG02886.hp2 HG03453.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2650+5775C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778874 | ||||||
chr10:68778882
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2650+5783C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778882 | ||||||
chr10:68779146
|
A | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+6047A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779146 | ||||||
chr10:68779230
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2650+6131A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779230 | ||||||
chr10:68779261
|
CT | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2650+6176delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68779261 | |||||
chr10:68779296
|
C | T | 3 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0056 | 3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2650+6197C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779296 | ||||||
chr10:68779367
|
C | T | 1 | a0001c0003t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2650+6268C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779367 | ||||||
chr10:68779372
|
C | G | 2 | a0001c0003t0002g0064a0001c0003t0002g0065 | 2 | HG01081.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2650+6273C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779372 | ||||||
chr10:68779414
|
A | T | 5 | a0001c0003t0002g0073a0001c0003t0002g0074a0001c0003t0002g0075others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+6315A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779414 | ||||||
chr10:68779526
|
C | T | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0009g0013 | 3 | HG01346.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+6427C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779526 | ||||||
chr10:68779632
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2651-6504G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779632 | ||||||
chr10:68779772
|
A | G | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2651-6364A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779772 | ||||||
chr10:68779938
|
T | C | 9 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(6): Show | 9 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-6198T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779938 | ||||||
chr10:68779987
|
ACT | A | 3 | a0001c0002t0001g0137a0001c0002t0001g0148a0001c0002t0001g0149 | 3 | NA18980.hp1 NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2651-6145_2651-614 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68779987 | |||||
chr10:68780079
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(2): Show | 5 | HG01934.hp1 NA18747.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2651-6057G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780079 | ||||||
chr10:68780172
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2651-5964A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780172 | ||||||
chr10:68780231
|
T | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2651-5905T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780231 | ||||||
chr10:68780297
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2651-5839T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780297 | ||||||
chr10:68780464
|
A | G | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2651-5672A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780464 | ||||||
chr10:68780503
|
T | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0100 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2651-5633T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780503 | ||||||
chr10:68780594
|
G | T | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2651-5542G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780594 | ||||||
chr10:68780737
|
A | G | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2651-5399A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780737 | ||||||
chr10:68780867
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2651-5269A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780867 | ||||||
chr10:68780875
|
G | A | 7 | a0001c0003t0002g0066a0001c0003t0004g0067a0001c0003t0004g0068others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2651-5261G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780875 | ||||||
chr10:68780901
|
A | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-5235A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780901 | ||||||
chr10:68781105
|
G | A | 10 | a0001c0001t0001g0163a0001c0001t0001g0219a0001c0001t0001g0223others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2651-5031G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781105 | ||||||
chr10:68781226
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2651-4910C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781226 | ||||||
chr10:68781278
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2651-4858C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781278 | ||||||
chr10:68781400
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2651-4736G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781400 | ||||||
chr10:68781436
|
G | A | 2 | a0001c0001t0001g0345a0001c0003t0001g0337 | 2 | HG01175.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2651-4700G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781436 | ||||||
chr10:68781505
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2651-4631G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781505 | ||||||
chr10:68781624
|
C | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-4512C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781624 | ||||||
chr10:68781657
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2651-4479C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781657 | ||||||
chr10:68781844
|
C | CT | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2651-4291dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68781844 | |||||
chr10:68781987
|
C | G | 1 | a0001c0002t0001g0145 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2651-4149C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781987 | ||||||
chr10:68782207
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2651-3929A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782207 | ||||||
chr10:68782279
|
A | G | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2651-3857A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782279 | ||||||
chr10:68782321
|
G | A | 1 | a0001c0002t0001g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2651-3815G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782321 | ||||||
chr10:68782709
|
T | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0196others(10): Show | 14 | NA18939.hp1 NA18940.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.2651-3427T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782709 | ||||||
chr10:68782821
|
T | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0297 | 2 | HG01243.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2651-3315T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782821 | ||||||
chr10:68782833
|
G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-3303G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782833 | ||||||
chr10:68782882
|
T | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2651-3254T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782882 | ||||||
chr10:68783000
|
CT | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2651-3116delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68783000 | |||||
chr10:68783114
|
C | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2651-3022C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783114 | ||||||
chr10:68783212
|
C | T | 8 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(5): Show | 8 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.2651-2924C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783212 | ||||||
chr10:68783267
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2651-2869G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783267 | ||||||
chr10:68783322
|
C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-2814C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783322 | ||||||
chr10:68783323
|
A | G | 39 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2651-2813A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783323 | ||||||
chr10:68783371
|
C | A | 1 | a0001c0001t0001g0287 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2651-2765C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783371 | ||||||
chr10:68783482
|
T | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-2654T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783482 | ||||||
chr10:68783519
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2651-2617A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783519 | ||||||
chr10:68783528
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2651-2608A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783528 | ||||||
chr10:68783588
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2651-2548T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783588 | ||||||
chr10:68783638
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2651-2498A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783638 | ||||||
chr10:68783696
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0193a0001c0001t0001g0336 | 3 | HG01071.hp2 HG02300.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2651-2440A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783696 | ||||||
chr10:68783844
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2651-2292G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783844 | ||||||
chr10:68783899
|
C | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2651-2237C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783899 | ||||||
chr10:68783949
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2651-2187G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783949 | ||||||
chr10:68783999
|
C | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-2137C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783999 | ||||||
chr10:68784001
|
G | A | 1 | a0001c0003t0002g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2651-2135G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784001 | ||||||
chr10:68784271
|
A | C | 1 | a0001c0007t0001g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2651-1865A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784271 | ||||||
chr10:68784286
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2651-1850G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784286 | ||||||
chr10:68784446
|
T | C | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-1690T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784446 | ||||||
chr10:68784506
|
T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-1630T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784506 | ||||||
chr10:68784561
|
A | G | 1 | a0001c0003t0002g0060 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2651-1575A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784561 | ||||||
chr10:68784650
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0193a0001c0001t0001g0336 | 3 | HG01071.hp2 HG02300.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2651-1486G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784650 | ||||||
chr10:68784690
|
A | C | 1 | a0001c0001t0003g0041 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2651-1446A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784690 | ||||||
chr10:68784703
|
T | C | 1 | a0002c0005t0008g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2651-1433T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784703 | ||||||
chr10:68784706
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2651-1430G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784706 | ||||||
chr10:68784714
|
C | A | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-1422C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784714 | ||||||
chr10:68784792
|
G | T | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108 | 3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2651-1344G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784792 | ||||||
chr10:68784821
|
T | C | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2651-1315T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784821 | ||||||
chr10:68784915
|
C | CT | 9 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0276others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2651-1201dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68784915 | |||||
chr10:68784915
|
CT | C | 90 | a0001c0001t0001g0034a0001c0001t0001g0082a0001c0001t0001g0083others(87): Show | 90 | HG00544.hp1 HG01081.hp1 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.2651-1201delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68784915 | |||||
chr10:68784915
|
CTT | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(34): Show | 38 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.2651-1202_2651-120 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68784915 | |||||
chr10:68784921
|
T | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-1215T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784921 | ||||||
chr10:68784942
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0016g0028 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2651-1194G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784942 | ||||||
chr10:68784961
|
C | T | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2651-1175C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784961 | ||||||
chr10:68784962
|
G | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2651-1174G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784962 | ||||||
chr10:68784991
|
C | A | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2651-1145C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784991 | ||||||
chr10:68785043
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2651-1093G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785043 | ||||||
chr10:68785044
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2651-1092A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785044 | ||||||
chr10:68785074
|
T | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2651-1062T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785074 | ||||||
chr10:68785184
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2651-952T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785184 | ||||||
chr10:68785192
|
C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-944C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785192 | ||||||
chr10:68785251
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2651-885C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785251 | ||||||
chr10:68785282
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0009g0013 | 3 | HG01069.hp1 HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2651-854A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785282 | ||||||
chr10:68785365
|
C | T | 1 | a0001c0002t0001g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2651-771C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785365 | ||||||
chr10:68785522
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2651-614G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785522 | ||||||
chr10:68785524
|
A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2651-612A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785524 | ||||||
chr10:68785691
|
A | G | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-445A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785691 | ||||||
chr10:68785862
|
A | T | 2 | a0001c0001t0001g0285a0001c0001t0001g0305 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2651-274A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785862 | ||||||
chr10:68785943
|
TTTG | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0216 | 3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2651-181_2651-179d others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68785943 | |||||
chr10:68786297
|
T | G | 6 | a0001c0001t0001g0301a0001c0001t0001g0306a0001c0001t0001g0307others(3): Show | 6 | HG01433.hp1 HG02630.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2733+79T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786297 | ||||||
chr10:68786351
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2733+133G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786351 | ||||||
chr10:68786372
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2733+154T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786372 | ||||||
chr10:68786399
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2734-147G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786399 | ||||||
chr10:68786466
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2734-80C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786466 | ||||||
chr10:68786475
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2734-71C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786475 | ||||||
chr10:68786491
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2734-55G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786491 | ||||||
chr10:68786756
|
G | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2880+64G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68786756 | ||||||
chr10:68786855
|
C | T | 7 | a0001c0002t0001g0115a0001c0002t0001g0122a0001c0002t0001g0127others(4): Show | 7 | NA18947.hp2 NA18949.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2880+163C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68786855 | ||||||
chr10:68786958
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2880+266G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68786958 | ||||||
chr10:68787019
|
A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2880+327A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787019 | ||||||
chr10:68787027
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2880+335A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787027 | ||||||
chr10:68787194
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2880+502T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787194 | ||||||
chr10:68787295
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0199a0001c0001t0001g0251 | 3 | NA18975.hp1 NA18982.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2880+603C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787295 | ||||||
chr10:68787526
|
A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2881-401A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787526 | ||||||
chr10:68787530
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2881-397A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787530 | ||||||
chr10:68787703
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2881-224C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787703 | ||||||
chr10:68787712
|
G | A | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2881-215G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787712 | ||||||
chr10:68787727
|
C | T | 1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2881-200C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787727 | ||||||
chr10:68787765
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2881-162G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787765 | ||||||
chr10:68787813
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2881-114C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787813 | ||||||
chr10:68788131
|
TTTATA | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0023others(3): Show | 6 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(3): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.3002-6_3002-2delTT others(3): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr10 | 68788131 | |||||
chr10:68788367
|
C | T | 2 | a0001c0003t0002g0061a0001c0003t0002g0063 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3187+39C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788367 | ||||||
chr10:68788672
|
A | G | 7 | a0001c0003t0002g0066a0001c0003t0004g0067a0001c0003t0004g0068others(4): Show | 7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3187+344A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788672 | ||||||
chr10:68788673
|
T | C | 3 | a0001c0001t0007g0350a0001c0001t0007g0351a0001c0001t0010g0353 | 3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3187+345T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788673 | ||||||
chr10:68788871
|
T | C | 1 | a0001c0003t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3187+543T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788871 | ||||||
chr10:68788908
|
G | A | 9 | a0001c0003t0002g0064a0001c0003t0002g0065a0001c0003t0002g0066others(6): Show | 9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3187+580G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788908 | ||||||
chr10:68789399
|
C | T | 1 | a0001c0002t0001g0151 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3188-311C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789399 | ||||||
chr10:68789459
|
C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3188-251C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789459 | ||||||
chr10:68789481
|
A | T | 2 | a0001c0001t0007g0350a0001c0001t0007g0351 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.3188-229A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789481 | ||||||
chr10:68789516
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.3188-194G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789516 | ||||||
chr10:68789613
|
A | G | 1 | a0001c0002t0001g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3188-97A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789613 | ||||||
chr10:68790004
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3393+89G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790004 | ||||||
chr10:68790354
|
T | TA | 10 | a0001c0001t0001g0289a0001c0001t0001g0303a0001c0001t0001g0313others(7): Show | 10 | HG01934.hp2 HG02293.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.3393+455dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790354 | |||||
chr10:68790354
|
TA | T | 7 | a0001c0001t0001g0195a0001c0001t0001g0276a0001c0001t0007g0350others(4): Show | 7 | HG00099.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3393+455delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790354 | |||||
chr10:68790418
|
A | G | 36 | a0001c0003t0002g0047a0001c0003t0002g0048a0001c0003t0002g0051others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.3393+503A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790418 | ||||||
chr10:68790553
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3393+638G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790553 | ||||||
chr10:68790589
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3394-618C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790589 | ||||||
chr10:68790804
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(164): Show | 168 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.3394-403T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790804 | ||||||
chr10:68790864
|
C | CA | 8 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0037others(5): Show | 8 | HG01361.hp1 HG02602.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.3394-327dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790864 | |||||
chr10:68790864
|
CA | C | 23 | a0001c0001t0001g0191a0001c0001t0001g0249a0001c0001t0001g0276others(20): Show | 23 | HG00558.hp1 HG00639.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.3394-327delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790864 | |||||
chr10:68790887
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3394-320C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790887 |