geneid | 9793 |
---|---|
ensemblid | ENSG00000175216.15 |
hgncid | 28959 |
symbol | CKAP5 |
name | cytoskeleton associated protein 5 |
refseq_nuc | NM_001008938.4 |
refseq_prot | NP_001008938.1 |
ensembl_nuc | ENST00000529230.6 |
ensembl_prot | ENSP00000432768.1 |
mane_status | MANE Select |
chr | chr11 |
start | 46743048 |
end | 46846280 |
strand | - |
ver | v1.2 |
region | chr11:46743048-46846280 |
region5000 | chr11:46738048-46851280 |
regionname0 | CKAP5_chr11_46743048_46846280 |
regionname5000 | CKAP5_chr11_46738048_46851280 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2032 | 290 | 90 | 58 | 112 | 8 | 20 | 92 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0002 | 0/0 | 2032 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0003 | 0/0 | 2032 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0004 | 0/0 | 2032 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0005 | 0/0 | 2032 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 6099 | 220 | 57 | 51 | 92 | 7 | 11 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0002 | 0/0 | 6099 | 37 | 27 | 5 | 0 | 1 | 4 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0003 | 0/0 | 6099 | 13 | 1 | 1 | 8 | 0 | 3 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0004 | 0/0 | 6099 | 9 | 0 | 0 | 9 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0005 | 0/0 | 6099 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0006 | 0/0 | 6099 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0007 | 0/0 | 6099 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0008 | 0/0 | 6099 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0009 | 0/0 | 6099 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0010 | 0/0 | 6099 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0011 | 0/0 | 6099 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0012 | 0/0 | 6099 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0013 | 0/0 | 6099 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0014 | 0/0 | 6099 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
c0015 | 0/0 | 6099 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1069 | 164 | 54 | 35 | 59 | 6 | 10 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0002 | 0/1 | 1074 | 73 | 1 | 16 | 49 | 1 | 5 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0003 | 1/0 | 1074 | 46 | 33 | 6 | 0 | 1 | 5 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0004 | 0/0 | 1074 | 5 | 0 | 0 | 5 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0005 | 0/0 | 1069 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0006 | 0/0 | 1074 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0007 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0008 | 0/0 | 1069 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0009 | 0/0 | 1069 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
t0010 | 0/0 | 1069 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 6099 | 220 | 57 | 51 | 92 | 7 | 11 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0002 | 0/0 | 6099 | 37 | 27 | 5 | 0 | 1 | 4 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0003 | 0/0 | 6099 | 13 | 1 | 1 | 8 | 0 | 3 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0004 | 0/0 | 6099 | 9 | 0 | 0 | 9 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0005 | 0/0 | 6099 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0006 | 0/0 | 6099 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0007 | 0/0 | 6099 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0008 | 0/0 | 6099 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0010 | 0/0 | 6099 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0013 | 0/0 | 6099 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0014 | 0/0 | 6099 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0002c0012 | 0/0 | 6099 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0003c0009 | 0/0 | 6099 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0004c0011 | 0/0 | 6099 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0005c0015 | 0/0 | 6099 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7167 | 142 | 49 | 33 | 47 | 6 | 7 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0001t0002 | 0/1 | 7172 | 62 | 1 | 16 | 39 | 1 | 4 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0001t0003 | 1/0 | 7172 | 7 | 5 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0001t0004 | 0/0 | 7172 | 5 | 0 | 0 | 5 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0001t0006 | 0/0 | 7172 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0001t0007 | 0/0 | 7172 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0001t0009 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0001t0010 | 0/0 | 7167 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0002t0003 | 0/0 | 7172 | 37 | 27 | 5 | 0 | 1 | 4 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0003t0001 | 0/0 | 7167 | 13 | 1 | 1 | 8 | 0 | 3 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0004t0002 | 0/0 | 7172 | 9 | 0 | 0 | 9 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0005t0001 | 0/0 | 7167 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0006t0005 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0006t0008 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0007t0001 | 0/0 | 7167 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0008t0003 | 0/0 | 7172 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0010t0002 | 0/0 | 7172 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0013t0003 | 0/0 | 7172 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0001c0014t0001 | 0/0 | 7167 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0002c0012t0001 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0003c0009t0001 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0004c0011t0002 | 0/0 | 7172 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
a0005c0015t0001 | 0/0 | 7167 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | copy fasta | chr11 | 46738048 | 46851280 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0003g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0001t0010g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0002t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0004t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0006t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0006t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0007t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0007t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0008t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0010t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0013t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0001c0014t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0002c0012t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0003c0009t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0004c0011t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
a0005c0015t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | FIN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00597 | hp1 | a0001 | c0004 | t0002 | g0106 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0251 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0132 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00738 | hp2 | a0001 | c0001 | t0010 | g0290 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0121 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01109 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01192 | hp1 | a0001 | c0014 | t0001 | g0243 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0139 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0215 | AMR | CLM | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01515 | hp1 | a0001 | c0002 | t0003 | g0122 | EUR | IBS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0264 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0126 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02055 | hp1 | a0003 | c0009 | t0001 | g0241 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0269 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0247 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0286 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CDX | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02257 | hp1 | a0001 | c0002 | t0003 | g0137 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02258 | hp1 | a0001 | c0002 | t0003 | g0138 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0274 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02572 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0140 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0263 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02818 | hp1 | a0001 | c0002 | t0003 | g0275 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0127 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0262 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02896 | hp1 | a0001 | c0006 | t0008 | g0289 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02965 | hp1 | a0001 | c0008 | t0003 | g0108 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02965 | hp2 | a0001 | c0007 | t0001 | g0233 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0123 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03017 | hp2 | a0001 | c0010 | t0002 | g0057 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0118 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03098 | hp2 | a0001 | c0006 | t0005 | g0288 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0135 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03139 | hp1 | a0001 | c0007 | t0001 | g0234 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0272 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0125 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03516 | hp1 | a0001 | c0002 | t0003 | g0136 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0265 | AFR | GWD | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03579 | hp2 | a0001 | c0002 | t0003 | g0273 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0204 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0141 | SAS | STU | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03704 | hp2 | a0001 | c0002 | t0003 | g0120 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03710 | hp2 | a0001 | c0013 | t0003 | g0131 | SAS | PJL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | BEB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0216 | SAS | STU | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0124 | SAS | STU | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | STU | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0207 | SAS | STU | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0214 | AFR | YRI | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0119 | AFR | YRI | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18960 | hp2 | a0001 | c0005 | t0001 | g0032 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18962 | hp2 | a0005 | c0015 | t0001 | g0287 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18967 | hp1 | a0001 | c0004 | t0002 | g0092 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18978 | hp1 | a0001 | c0005 | t0001 | g0034 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18982 | hp1 | a0004 | c0011 | t0002 | g0088 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18982 | hp2 | a0001 | c0004 | t0002 | g0047 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18984 | hp2 | a0001 | c0005 | t0001 | g0033 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18987 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19007 | hp1 | a0001 | c0004 | t0002 | g0086 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19011 | hp1 | a0001 | c0004 | t0002 | g0085 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0266 | AFR | LWK | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | LWK | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19063 | hp2 | a0001 | c0004 | t0002 | g0087 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19077 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19080 | hp2 | a0001 | c0004 | t0002 | g0084 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19083 | hp2 | a0001 | c0004 | t0002 | g0116 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19091 | hp2 | a0001 | c0004 | t0002 | g0115 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA19240 | hp2 | a0002 | c0012 | t0001 | g0276 | AFR | YRI | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0130 | AFR | ASW | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ASW | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0134 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0133 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0129 | AFR | USA | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0071 | REF | REF | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0281 | REF | REF | CKAP5_chr11_46738048_46851280 | CKAP5 | chr11 | 46738048 | 46851280 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46759038
|
C | T | 1 | a0003 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.4574G>A | p.Arg1525Gln | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/44 | 4672/7172 | 4574/6099 | 1525/2032 | chr11 | 46759038 | ||
chr11:46759353
|
T | C | 1 | a0004 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.4484A>G | p.Asn1495Ser | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 34/44 | 4582/7172 | 4484/6099 | 1495/2032 | chr11 | 46759353 | ||
chr11:46765256
|
T | A | 1 | a0002 | 1 | NA19240.hp2 | missense_variant&splice_region_variant | MODERATE | c.3412A>T | p.Ser1138Cys | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/44 | 3510/7172 | 3412/6099 | 1138/2032 | chr11 | 46765256 | ||
chr11:46816204
|
G | A | 1 | a0005 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.452C>T | p.Ala151Val | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/44 | 550/7172 | 452/6099 | 151/2032 | chr11 | 46816204 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46751220
|
G | A | 1 | a0001c0006 | 2 | HG02896.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.5358C>T | p.Asn1786Asn | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 40/44 | 5456/7172 | 5358/6099 | 1786/2032 | chr11 | 46751220 | ||
chr11:46751238
|
C | T | 1 | a0001c0010 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.5340G>A | p.Thr1780Thr | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 40/44 | 5438/7172 | 5340/6099 | 1780/2032 | chr11 | 46751238 | ||
chr11:46751513
|
G | A | 1 | a0001c0006 | 2 | HG02896.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.5155C>T | p.Leu1719Leu | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 39/44 | 5253/7172 | 5155/6099 | 1719/2032 | chr11 | 46751513 | ||
chr11:46759019
|
G | A | 1 | a0001c0004 | 9 | HG00597.hp1 NA18967.hp1 NA18982.hp2 others(6): Show |
synonymous_variant | LOW | c.4593C>T | p.Phe1531Phe | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/44 | 4691/7172 | 4593/6099 | 1531/2032 | chr11 | 46759019 | ||
chr11:46760629
|
G | A | 1 | a0001c0003 | 13 | HG00609.hp1 HG01496.hp2 HG03654.hp1 others(10): Show |
synonymous_variant | LOW | c.4377C>T | p.Asp1459Asp | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 33/44 | 4475/7172 | 4377/6099 | 1459/2032 | chr11 | 46760629 | ||
chr11:46763138
|
A | G | 1 | a0001c0008 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.3729T>C | p.Asp1243Asp | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 30/44 | 3827/7172 | 3729/6099 | 1243/2032 | chr11 | 46763138 | ||
chr11:46763147
|
A | C | 2 | a0001c0002a0001c0013 | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
synonymous_variant | LOW | c.3720T>G | p.Gly1240Gly | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 30/44 | 3818/7172 | 3720/6099 | 1240/2032 | chr11 | 46763147 | ||
chr11:46776294
|
A | G | 1 | a0001c0006 | 2 | HG02896.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.2952T>C | p.Ser984Ser | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/44 | 3050/7172 | 2952/6099 | 984/2032 | chr11 | 46776294 | ||
chr11:46776336
|
T | C | 1 | a0001c0007 | 2 | HG02965.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.2910A>G | p.Glu970Glu | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/44 | 3008/7172 | 2910/6099 | 970/2032 | chr11 | 46776336 | ||
chr11:46778142
|
G | T | 1 | a0001c0005 | 3 | NA18960.hp2 NA18978.hp1 NA18984.hp2 |
synonymous_variant | LOW | c.2745C>A | p.Ile915Ile | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 22/44 | 2843/7172 | 2745/6099 | 915/2032 | chr11 | 46778142 | ||
chr11:46790572
|
T | C | 1 | a0001c0013 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1662A>G | p.Pro554Pro | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 14/44 | 1760/7172 | 1662/6099 | 554/2032 | chr11 | 46790572 | ||
chr11:46808046
|
T | C | 1 | a0001c0014 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.963A>G | p.Val321Val | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/44 | 1061/7172 | 963/6099 | 321/2032 | chr11 | 46808046 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46743099
|
C | T | 6 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(3): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*924G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 924 | chr11 | 46743099 | |||||
chr11:46743263
|
C | T | 1 | a0001c0001t0004 | 5 | NA18949.hp2 NA18973.hp2 NA18978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 760 | chr11 | 46743263 | |||||
chr11:46743269
|
G | A | 2 | a0001c0006t0005a0001c0006t0008 | 2 | HG02896.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*754C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 754 | chr11 | 46743269 | |||||
chr11:46743393
|
G | T | 1 | a0001c0001t0007 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*630C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 630 | chr11 | 46743393 | |||||
chr11:46743734
|
AAAAAG | A | 12 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(9): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*284_*288delCTTTT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 284 | chr11 | 46743734 | |||||
chr11:46743765
|
C | A | 2 | a0001c0006t0005a0001c0006t0008 | 2 | HG02896.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*258G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 258 | chr11 | 46743765 | |||||
chr11:46743842
|
G | A | 1 | a0001c0001t0009 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 181 | chr11 | 46743842 | |||||
chr11:46743901
|
G | T | 1 | a0001c0001t0006 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 122 | chr11 | 46743901 | |||||
chr11:46743907
|
C | T | 1 | a0001c0006t0005 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 44/44 | 116 | chr11 | 46743907 | |||||
chr11:46846271
|
G | A | 1 | a0001c0001t0010 | 1 | HG00738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-89C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/44 | 25040 | chr11 | 46846271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46744400
|
A | G | 7 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(4): Show | 7 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.5856+26T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 43/43 | chr11 | 46744400 | ||||||
chr11:46744719
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5705-142A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46744719 | ||||||
chr11:46745092
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5705-515G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745092 | ||||||
chr11:46745151
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0173 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5705-574T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745151 | ||||||
chr11:46745201
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5705-624C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745201 | ||||||
chr11:46745230
|
A | G | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.5705-653T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745230 | ||||||
chr11:46745340
|
T | C | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(30): Show | 33 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.5705-763A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745340 | ||||||
chr11:46745379
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5705-802A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745379 | ||||||
chr11:46745504
|
C | T | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5705-927G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745504 | ||||||
chr11:46745959
|
C | A | 1 | a0001c0001t0001g0042 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5705-1382G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745959 | ||||||
chr11:46745987
|
C | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0284 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5705-1410G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46745987 | ||||||
chr11:46746152
|
A | G | 1 | a0001c0002t0003g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5705-1575T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746152 | ||||||
chr11:46746200
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.5705-1623T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746200 | ||||||
chr11:46746300
|
G | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5705-1723C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746300 | ||||||
chr11:46746323
|
A | G | 4 | a0001c0003t0001g0206a0001c0003t0001g0251a0001c0003t0001g0252others(1): Show | 4 | HG00609.hp1 NA18971.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.5705-1746T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746323 | ||||||
chr11:46746399
|
C | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.5705-1822G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746399 | ||||||
chr11:46746491
|
A | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.5705-1914T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746491 | ||||||
chr11:46746556
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5705-1979T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746556 | ||||||
chr11:46746618
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.5705-2041A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746618 | ||||||
chr11:46746623
|
A | G | 9 | a0001c0002t0003g0118a0001c0002t0003g0119a0001c0002t0003g0128others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.5705-2046T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746623 | ||||||
chr11:46746855
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.5705-2278C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746855 | ||||||
chr11:46746903
|
G | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.5705-2326C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46746903 | ||||||
chr11:46747600
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5704+2674A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46747600 | ||||||
chr11:46747601
|
C | CA | 7 | a0001c0001t0001g0041a0001c0001t0001g0167a0001c0001t0001g0277others(4): Show | 7 | HG00673.hp1 HG01109.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.5704+2672dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46747601 | ||||||
chr11:46747633
|
G | T | 1 | a0001c0004t0002g0115 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.5704+2641C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46747633 | ||||||
chr11:46747704
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5704+2570T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46747704 | ||||||
chr11:46747705
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5704+2569A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46747705 | ||||||
chr11:46747752
|
G | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5704+2522C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46747752 | ||||||
chr11:46747825
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5704+2449G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46747825 | ||||||
chr11:46748106
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5704+2168C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748106 | ||||||
chr11:46748205
|
G | T | 1 | a0001c0001t0003g0218 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5704+2069C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748205 | ||||||
chr11:46748238
|
A | C | 79 | a0001c0001t0001g0200a0001c0001t0002g0001a0001c0001t0002g0017others(76): Show | 80 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.5704+2036T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748238 | ||||||
chr11:46748330
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5704+1944C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748330 | ||||||
chr11:46748527
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5704+1747T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748527 | ||||||
chr11:46748643
|
T | C | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5704+1631A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748643 | ||||||
chr11:46748809
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.5704+1465G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748809 | ||||||
chr11:46748810
|
G | A | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5704+1464C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748810 | ||||||
chr11:46748814
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5704+1460A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748814 | ||||||
chr11:46748870
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5704+1404G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748870 | ||||||
chr11:46748917
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5704+1357G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748917 | ||||||
chr11:46748966
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0001g0238 | 3 | NA18949.hp1 NA18977.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.5704+1308C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46748966 | ||||||
chr11:46749275
|
A | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.5704+999T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46749275 | ||||||
chr11:46749275
|
A | T | 1 | a0001c0004t0002g0085 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.5704+999T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46749275 | ||||||
chr11:46749327
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5704+947G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46749327 | ||||||
chr11:46749457
|
G | GA | 122 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0031others(119): Show | 124 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.5704+816dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46749457 | ||||||
chr11:46749457
|
G | GAA | 12 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(9): Show | 12 | HG01109.hp1 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.5704+815_5704+816d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46749457 | ||||||
chr11:46749808
|
T | G | 44 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(41): Show | 45 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.5704+466A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46749808 | ||||||
chr11:46749880
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.5704+394A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46749880 | ||||||
chr11:46750081
|
C | A | 2 | a0001c0003t0001g0214a0001c0003t0001g0215 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5704+193G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46750081 | ||||||
chr11:46750222
|
G | A | 1 | a0001c0014t0001g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5704+52C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 42/43 | chr11 | 46750222 | ||||||
chr11:46750778
|
T | G | 1 | a0001c0001t0006g0100 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5461-167A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 40/43 | chr11 | 46750778 | ||||||
chr11:46750961
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.5460+157C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 40/43 | chr11 | 46750961 | ||||||
chr11:46750986
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5460+132C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 40/43 | chr11 | 46750986 | ||||||
chr11:46751804
|
T | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.5134-270A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46751804 | ||||||
chr11:46751830
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.5134-296C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46751830 | ||||||
chr11:46752100
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5133+535C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752100 | ||||||
chr11:46752161
|
C | CATATATA others(1): Show |
6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0226others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+466_5133+473d others(10): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0229 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5133+464_5133+473d others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
C | CATATATA others(5): Show |
9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 9 | HG01192.hp1 HG02004.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.5133+462_5133+473d others(14): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
C | CATATATA others(7): Show |
1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5133+460_5133+473d others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
C | CATATATA others(11): Show |
2 | a0001c0001t0001g0230a0001c0001t0003g0218 | 2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.5133+456_5133+473d others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
CAT | C | 5 | a0001c0001t0001g0143a0001c0001t0001g0157a0001c0001t0001g0161others(2): Show | 5 | HG00558.hp2 HG02647.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.5133+472_5133+473d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
CATAT | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0002g0001others(5): Show | 9 | HG00609.hp2 HG00673.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.5133+470_5133+473d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0002g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5133+464_5133+473d others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0232a0001c0002t0003g0122 | 2 | HG01515.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5133+462_5133+473d others(14): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
CATATATA others(7): Show |
C | 5 | a0001c0002t0003g0120a0001c0002t0003g0123a0001c0002t0003g0132others(2): Show | 5 | HG00735.hp1 HG01257.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.5133+460_5133+473d others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752161
|
CATATATA others(11): Show |
C | 27 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(24): Show | 28 | HG01074.hp2 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.5133+456_5133+473d others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752161 | ||||||
chr11:46752183
|
T | C | 5 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0049others(2): Show | 6 | HG00609.hp2 HG00673.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.5133+452A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752183 | ||||||
chr11:46752185
|
T | C | 5 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0049others(2): Show | 6 | HG00609.hp2 HG00673.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.5133+450A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752185 | ||||||
chr11:46752185
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0277 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5133+440_5133+449d others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752185 | ||||||
chr11:46752185
|
TATATATA others(11): Show |
T | 3 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5133+432_5133+449d others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752185 | ||||||
chr11:46752187
|
T | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0167a0001c0001t0002g0001others(6): Show | 10 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.5133+448A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752187 | ||||||
chr11:46752187
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5133+438_5133+447d others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752187 | ||||||
chr11:46752189
|
T | C | 31 | a0001c0001t0001g0027a0001c0001t0001g0149a0001c0001t0001g0150others(28): Show | 32 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.5133+446A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752189 | ||||||
chr11:46752191
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(87): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.5133+444A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752191 | ||||||
chr11:46752193
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(111): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.5133+442A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATACACA others(7): Show |
1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATACA others(7): Show |
2 | a0001c0001t0002g0078a0001c0001t0002g0097 | 2 | HG00438.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATACA others(11): Show |
1 | a0001c0001t0002g0059 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATACA others(5): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(14): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(5): Show |
1 | a0001c0001t0002g0035 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(14): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(7): Show |
1 | a0001c0004t0002g0092 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(9): Show |
6 | a0001c0001t0002g0046a0001c0001t0002g0053a0001c0001t0002g0054others(3): Show | 6 | HG01192.hp2 HG03704.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(18): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(11): Show |
6 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0066others(3): Show | 6 | NA18961.hp2 NA18982.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(13): Show |
2 | a0001c0001t0002g0098a0001c0004t0002g0085 | 2 | NA18991.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(22): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0025 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(3): Show |
2 | a0001c0001t0001g0239a0001c0002t0003g0275 | 2 | HG02602.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(7): Show |
1 | a0001c0001t0002g0039 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(9): Show |
4 | a0001c0001t0001g0171a0001c0001t0001g0267a0001c0001t0002g0050others(1): Show | 4 | HG03471.hp1 HG03579.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(18): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(11): Show |
15 | a0001c0001t0002g0040a0001c0001t0002g0060a0001c0001t0002g0062others(12): Show | 15 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(13): Show |
6 | a0001c0001t0002g0056a0001c0001t0002g0073a0001c0001t0002g0076others(3): Show | 6 | HG00597.hp1 HG01978.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(22): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(17): Show |
1 | a0001c0001t0002g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(26): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5133+441_5133+442i others(14): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(7): Show |
3 | a0001c0001t0001g0235a0001c0007t0001g0233a0001c0007t0001g0234 | 3 | HG02572.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(9): Show |
3 | a0001c0001t0001g0240a0001c0001t0002g0071a0001c0001t0009g0247 | 3 | HG02145.hp1 HG03516.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(18): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(11): Show |
1 | a0001c0001t0002g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(13): Show |
6 | a0001c0001t0002g0022a0001c0001t0002g0048a0001c0001t0002g0070others(3): Show | 6 | HG00280.hp2 HG00642.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(22): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(15): Show |
8 | a0001c0001t0002g0058a0001c0001t0002g0061a0001c0001t0002g0064others(5): Show | 8 | HG00733.hp2 HG01074.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(24): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(17): Show |
1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5133+441_5133+442i others(26): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(7): Show |
6 | a0001c0001t0001g0031a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG03471.hp2 NA18747.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(9): Show |
1 | a0001c0002t0003g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(18): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(13): Show |
2 | a0001c0001t0001g0172a0001c0001t0002g0065 | 2 | HG01993.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(22): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(15): Show |
6 | a0001c0001t0002g0037a0001c0001t0002g0095a0001c0001t0002g0101others(3): Show | 6 | HG02132.hp1 HG03017.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+441_5133+442i others(24): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(17): Show |
2 | a0001c0001t0002g0063a0001c0001t0002g0068 | 2 | HG01099.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(26): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(11): Show |
1 | a0001c0001t0001g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(17): Show |
1 | a0001c0001t0002g0017 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.5133+441_5133+442i others(26): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(19): Show |
1 | a0001c0004t0002g0116 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.5133+441_5133+442i others(28): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(11): Show |
2 | a0001c0001t0001g0008a0001c0002t0003g0273 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5133+441_5133+442i others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5133+441_5133+442i others(22): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0222 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.5133+441_5133+442i others(28): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752193
|
TACAC | T | 4 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 4 | HG02723.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5133+438_5133+441d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752193 | ||||||
chr11:46752195
|
C | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0228a0001c0001t0001g0244others(3): Show | 6 | HG01496.hp1 HG01884.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.5133+440G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752195 | ||||||
chr11:46752197
|
C | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0255a0001c0001t0001g0257others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.5133+438G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752197 | ||||||
chr11:46752199
|
C | T | 7 | a0001c0001t0001g0228a0001c0001t0001g0255a0001c0001t0001g0256others(4): Show | 7 | HG02622.hp2 HG02723.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.5133+436G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752199 | ||||||
chr11:46752201
|
C | T | 6 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG02622.hp2 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+434G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752201 | ||||||
chr11:46752203
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5133+432G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752203 | ||||||
chr11:46752219
|
C | CACACAT | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00280.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.5133+415_5133+416i others(8): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752219 | ||||||
chr11:46752219
|
C | CACAT | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0174others(3): Show | 6 | HG00738.hp1 HG00741.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+415_5133+416i others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752219 | ||||||
chr11:46752219
|
C | CAT | 33 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0145others(30): Show | 34 | HG00673.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.5133+415_5133+416i others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752219 | ||||||
chr11:46752219
|
C | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.5133+416G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752219 | ||||||
chr11:46752221
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0002g0072a0001c0006t0005g0288others(1): Show | 4 | HG01243.hp1 HG02273.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5133+414G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752221 | ||||||
chr11:46752225
|
C | T | 38 | a0001c0001t0002g0055a0001c0002t0003g0004a0001c0002t0003g0118others(35): Show | 39 | HG00621.hp1 HG00735.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.5133+410G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752225 | ||||||
chr11:46752462
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.5133+173G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752462 | ||||||
chr11:46752500
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5133+135G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 38/43 | chr11 | 46752500 | ||||||
chr11:46752975
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5058-265A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 37/43 | chr11 | 46752975 | ||||||
chr11:46752989
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5058-279C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 37/43 | chr11 | 46752989 | ||||||
chr11:46753081
|
A | C | 1 | a0001c0001t0002g0072 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5057+229T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 37/43 | chr11 | 46753081 | ||||||
chr11:46753122
|
C | T | 23 | a0001c0001t0001g0148a0001c0001t0001g0210a0001c0001t0001g0211others(20): Show | 23 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.5057+188G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 37/43 | chr11 | 46753122 | ||||||
chr11:46753202
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5057+108A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 37/43 | chr11 | 46753202 | ||||||
chr11:46753268
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5057+42G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 37/43 | chr11 | 46753268 | ||||||
chr11:46753593
|
T | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4870-96A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753593 | ||||||
chr11:46753610
|
G | A | 1 | a0001c0001t0004g0105 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4870-113C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753610 | ||||||
chr11:46753625
|
G | A | 1 | a0001c0001t0002g0089 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4870-128C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753625 | ||||||
chr11:46753711
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4870-214G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753711 | ||||||
chr11:46753740
|
C | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.4870-243G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753740 | ||||||
chr11:46753832
|
T | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.4870-335A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753832 | ||||||
chr11:46753871
|
C | T | 2 | a0001c0002t0003g0119a0001c0002t0003g0133 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4870-374G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753871 | ||||||
chr11:46753895
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4870-398A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46753895 | ||||||
chr11:46754248
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4869+640A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754248 | ||||||
chr11:46754297
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4869+591T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754297 | ||||||
chr11:46754329
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4869+559G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754329 | ||||||
chr11:46754376
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4869+512G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754376 | ||||||
chr11:46754543
|
A | G | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.4869+345T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754543 | ||||||
chr11:46754581
|
T | TTAGCATT others(246): Show |
1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4869+306_4869+307i others(255): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754581 | ||||||
chr11:46754582
|
T | G | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4869+306A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754582 | ||||||
chr11:46754600
|
CAT | C | 10 | a0001c0002t0003g0120a0001c0002t0003g0121a0001c0002t0003g0122others(7): Show | 10 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.4869+286_4869+287d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754600 | ||||||
chr11:46754626
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.4869+262A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754626 | ||||||
chr11:46754630
|
C | G | 3 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4869+258G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 36/43 | chr11 | 46754630 | ||||||
chr11:46755147
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.4690-80T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46755147 | ||||||
chr11:46755457
|
T | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4690-390A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46755457 | ||||||
chr11:46755550
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4690-483C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46755550 | ||||||
chr11:46755842
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.4690-775A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46755842 | ||||||
chr11:46755878
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4690-811C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46755878 | ||||||
chr11:46755885
|
C | T | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4690-818G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46755885 | ||||||
chr11:46756064
|
G | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.4690-997C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756064 | ||||||
chr11:46756100
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4690-1033C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756100 | ||||||
chr11:46756153
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4690-1086A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756153 | ||||||
chr11:46756408
|
T | C | 23 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(20): Show | 24 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.4690-1341A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756408 | ||||||
chr11:46756435
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4690-1368C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756435 | ||||||
chr11:46756560
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4690-1493G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756560 | ||||||
chr11:46756754
|
A | AT | 79 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0001g0147others(76): Show | 80 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.4690-1688dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756754 | ||||||
chr11:46756754
|
AT | A | 8 | a0001c0001t0001g0198a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG02723.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.4690-1688delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756754 | ||||||
chr11:46756755
|
T | TC | 36 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(33): Show | 37 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.4690-1689_4690-168 others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756755 | ||||||
chr11:46756756
|
T | C | 1 | a0001c0002t0003g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4690-1689A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756756 | ||||||
chr11:46756896
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4690-1829G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756896 | ||||||
chr11:46756917
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4690-1850C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756917 | ||||||
chr11:46756939
|
A | T | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4690-1872T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46756939 | ||||||
chr11:46757056
|
C | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4689+1867G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757056 | ||||||
chr11:46757130
|
T | C | 11 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(8): Show | 11 | HG00609.hp1 HG03654.hp1 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.4689+1793A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757130 | ||||||
chr11:46757205
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4689+1718A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757205 | ||||||
chr11:46757254
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4689+1669T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757254 | ||||||
chr11:46757461
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4689+1462G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757461 | ||||||
chr11:46757477
|
C | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4689+1446G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757477 | ||||||
chr11:46757656
|
C | T | 1 | a0001c0003t0001g0216 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4689+1267G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757656 | ||||||
chr11:46757741
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4689+1182G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757741 | ||||||
chr11:46757887
|
A | AT | 82 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0030others(79): Show | 83 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.4689+1035dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46757887 | ||||||
chr11:46758088
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4689+835A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758088 | ||||||
chr11:46758247
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4689+676G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758247 | ||||||
chr11:46758649
|
T | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4689+274A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758649 | ||||||
chr11:46758714
|
G | GA | 6 | a0001c0001t0002g0037a0001c0001t0002g0062a0001c0004t0002g0092others(3): Show | 6 | HG00741.hp2 HG02896.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.4689+208dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758714 | ||||||
chr11:46758714
|
GA | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.4689+208delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758714 | ||||||
chr11:46758728
|
A | T | 1 | a0001c0001t0009g0247 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4689+195T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758728 | ||||||
chr11:46758729
|
A | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4689+194T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758729 | ||||||
chr11:46758741
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4689+182T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758741 | ||||||
chr11:46758772
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4689+151T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758772 | ||||||
chr11:46758785
|
T | A | 1 | a0001c0001t0002g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4689+138A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758785 | ||||||
chr11:46758801
|
C | T | 1 | a0001c0002t0003g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4689+122G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758801 | ||||||
chr11:46758899
|
C | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0160 | 3 | HG02486.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4689+24G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 35/43 | chr11 | 46758899 | ||||||
chr11:46759100
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4569-57A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 34/43 | chr11 | 46759100 | ||||||
chr11:46759220
|
G | A | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4568+49C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 34/43 | chr11 | 46759220 | ||||||
chr11:46759259
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0249 | 3 | HG02630.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4568+10A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 34/43 | chr11 | 46759259 | ||||||
chr11:46759757
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4395-315A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 33/43 | chr11 | 46759757 | ||||||
chr11:46760168
|
A | T | 33 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(30): Show | 34 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.4394+444T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 33/43 | chr11 | 46760168 | ||||||
chr11:46760442
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4394+170T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 33/43 | chr11 | 46760442 | ||||||
chr11:46760921
|
A | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0001g0160 | 3 | HG02486.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4222-137T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46760921 | ||||||
chr11:46760922
|
C | A | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.4222-138G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46760922 | ||||||
chr11:46761010
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4222-226T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761010 | ||||||
chr11:46761120
|
G | A | 1 | a0001c0007t0001g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4222-336C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761120 | ||||||
chr11:46761190
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4222-406C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761190 | ||||||
chr11:46761248
|
C | CA | 47 | a0001c0001t0001g0041a0001c0001t0001g0109a0001c0001t0001g0148others(44): Show | 48 | HG00099.hp2 HG00735.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.4222-465dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761248 | ||||||
chr11:46761248
|
C | CAA | 20 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(17): Show | 20 | HG00609.hp1 HG00738.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.4222-466_4222-465d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761248 | ||||||
chr11:46761408
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.4221+592T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761408 | ||||||
chr11:46761454
|
A | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | NA18951.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.4221+546T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761454 | ||||||
chr11:46761487
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4221+513A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761487 | ||||||
chr11:46761676
|
G | A | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4221+324C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761676 | ||||||
chr11:46761885
|
T | C | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(30): Show | 33 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.4221+115A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 32/43 | chr11 | 46761885 | ||||||
chr11:46762465
|
A | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4027+162T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 31/43 | chr11 | 46762465 | ||||||
chr11:46762525
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4027+102G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 31/43 | chr11 | 46762525 | ||||||
chr11:46763401
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3687+80A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 29/43 | chr11 | 46763401 | ||||||
chr11:46763663
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3538-33C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46763663 | ||||||
chr11:46763914
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3538-284A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46763914 | ||||||
chr11:46763991
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3538-361T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46763991 | ||||||
chr11:46764143
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3538-513T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764143 | ||||||
chr11:46764155
|
GA | G | 6 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0179others(3): Show | 6 | HG02896.hp1 HG03098.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.3538-526delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764155 | ||||||
chr11:46764252
|
T | G | 1 | a0001c0003t0001g0252 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3538-622A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764252 | ||||||
chr11:46764580
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3537+551T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764580 | ||||||
chr11:46764883
|
A | ATCAATGA others(22): Show |
7 | a0001c0001t0001g0232a0001c0001t0001g0248a0001c0001t0002g0049others(4): Show | 7 | HG00621.hp1 HG02165.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3537+247_3537+248i others(31): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764883 | ||||||
chr11:46764885
|
T | A | 7 | a0001c0001t0001g0232a0001c0001t0001g0248a0001c0001t0002g0049others(4): Show | 7 | HG00621.hp1 HG02165.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3537+246A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764885 | ||||||
chr11:46764886
|
C | A | 7 | a0001c0001t0001g0232a0001c0001t0001g0248a0001c0001t0002g0049others(4): Show | 7 | HG00621.hp1 HG02165.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3537+245G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764886 | ||||||
chr11:46764886
|
C | CAATGAAT others(23): Show |
280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(277): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.3537+244_3537+245i others(32): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 28/43 | chr11 | 46764886 | ||||||
chr11:46765365
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0249 | 3 | HG02630.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3412-109C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46765365 | ||||||
chr11:46765599
|
CT | C | 22 | a0001c0001t0001g0030a0001c0001t0001g0148a0001c0001t0001g0150others(19): Show | 22 | HG00597.hp2 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.3412-344delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46765599 | ||||||
chr11:46765599
|
CTT | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.3412-345_3412-344d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46765599 | ||||||
chr11:46765599
|
CTTT | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0109others(12): Show | 15 | HG00673.hp1 HG01109.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.3412-346_3412-344d others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46765599 | ||||||
chr11:46765807
|
G | A | 6 | a0001c0001t0001g0180a0001c0001t0001g0197a0001c0001t0001g0198others(3): Show | 6 | HG00438.hp2 NA18947.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.3412-551C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46765807 | ||||||
chr11:46765824
|
C | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.3412-568G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46765824 | ||||||
chr11:46765856
|
C | G | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.3412-600G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46765856 | ||||||
chr11:46766023
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.3412-767A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46766023 | ||||||
chr11:46766145
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3412-889A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46766145 | ||||||
chr11:46766648
|
GCA | G | 10 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0210others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.3411+925_3411+926d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46766648 | ||||||
chr11:46766691
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3411+884G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46766691 | ||||||
chr11:46767020
|
G | GCTTT | 40 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(37): Show | 41 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.3411+551_3411+554d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767020 | ||||||
chr11:46767026
|
T | TTTC | 4 | a0001c0002t0003g0120a0001c0002t0003g0123a0001c0006t0005g0288others(1): Show | 4 | HG02896.hp1 HG03017.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3411+548_3411+549i others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767026 | ||||||
chr11:46767027
|
C | T | 4 | a0001c0002t0003g0120a0001c0002t0003g0123a0001c0006t0005g0288others(1): Show | 4 | HG02896.hp1 HG03017.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3411+548G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767027 | ||||||
chr11:46767029
|
T | C | 4 | a0001c0002t0003g0120a0001c0002t0003g0123a0001c0006t0005g0288others(1): Show | 4 | HG02896.hp1 HG03017.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3411+546A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767029 | ||||||
chr11:46767141
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.3411+434G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767141 | ||||||
chr11:46767263
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3411+312C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767263 | ||||||
chr11:46767272
|
G | T | 1 | a0001c0001t0002g0038 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3411+303C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767272 | ||||||
chr11:46767431
|
C | T | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3411+144G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767431 | ||||||
chr11:46767475
|
T | C | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3411+100A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 27/43 | chr11 | 46767475 | ||||||
chr11:46767796
|
G | GT | 38 | a0001c0001t0001g0250a0001c0002t0003g0004a0001c0002t0003g0118others(35): Show | 39 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.3323-134dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46767796 | ||||||
chr11:46767827
|
A | G | 1 | a0001c0007t0001g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3323-164T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46767827 | ||||||
chr11:46768063
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3323-400A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46768063 | ||||||
chr11:46768140
|
G | A | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3323-477C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46768140 | ||||||
chr11:46768240
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3323-577C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46768240 | ||||||
chr11:46768367
|
C | CT | 8 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0277others(5): Show | 8 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3323-705dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46768367 | ||||||
chr11:46768367
|
CT | C | 27 | a0001c0001t0002g0050a0001c0001t0002g0114a0001c0001t0004g0110others(24): Show | 28 | HG01070.hp2 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.3323-705delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46768367 | ||||||
chr11:46768902
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3322+1061T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46768902 | ||||||
chr11:46769023
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3322+940T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769023 | ||||||
chr11:46769107
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3322+856C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769107 | ||||||
chr11:46769445
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3322+518G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769445 | ||||||
chr11:46769533
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3322+430T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769533 | ||||||
chr11:46769564
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3322+399G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769564 | ||||||
chr11:46769591
|
G | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3322+372C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769591 | ||||||
chr11:46769628
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3322+335G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769628 | ||||||
chr11:46769784
|
C | A | 1 | a0001c0002t0003g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3322+179G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769784 | ||||||
chr11:46769852
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3322+111G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 26/43 | chr11 | 46769852 | ||||||
chr11:46770151
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3187-53T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 25/43 | chr11 | 46770151 | ||||||
chr11:46770307
|
T | C | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3187-209A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 25/43 | chr11 | 46770307 | ||||||
chr11:46770495
|
G | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3186+293C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 25/43 | chr11 | 46770495 | ||||||
chr11:46771100
|
T | G | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2992-118A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46771100 | ||||||
chr11:46771145
|
A | T | 44 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(41): Show | 45 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.2992-163T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46771145 | ||||||
chr11:46771283
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0173 | 2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2992-301C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46771283 | ||||||
chr11:46771933
|
G | A | 1 | a0001c0002t0003g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2992-951C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46771933 | ||||||
chr11:46771985
|
AAC | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2992-1005_2992-100 others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46771985 | ||||||
chr11:46772033
|
CT | C | 96 | a0001c0001t0001g0109a0001c0001t0001g0255a0001c0001t0001g0256others(93): Show | 97 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2992-1052delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772033 | ||||||
chr11:46772033
|
CTT | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.2992-1053_2992-105 others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772033 | ||||||
chr11:46772033
|
CTTT | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0148others(5): Show | 8 | HG01167.hp1 HG01167.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2992-1054_2992-105 others(7): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772033 | ||||||
chr11:46772132
|
T | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2992-1150A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772132 | ||||||
chr11:46772560
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2992-1578G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772560 | ||||||
chr11:46772733
|
C | CT | 74 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(71): Show | 75 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2992-1752dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772733 | ||||||
chr11:46772738
|
T | TTTTTTTT others(3): Show |
2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2992-1757_2992-175 others(14): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772738 | ||||||
chr11:46772837
|
G | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0161 | 2 | NA18964.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2992-1855C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772837 | ||||||
chr11:46772930
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2992-1948G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46772930 | ||||||
chr11:46773298
|
A | G | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2992-2316T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773298 | ||||||
chr11:46773335
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2992-2353G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773335 | ||||||
chr11:46773392
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0198 | 2 | NA19056.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2992-2410C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773392 | ||||||
chr11:46773437
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2992-2455A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773437 | ||||||
chr11:46773515
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2992-2533G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773515 | ||||||
chr11:46773596
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2992-2614T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773596 | ||||||
chr11:46773603
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2992-2621A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773603 | ||||||
chr11:46773680
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2991+2575G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773680 | ||||||
chr11:46773803
|
A | G | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2991+2452T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773803 | ||||||
chr11:46773809
|
C | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG01258.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2991+2446G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773809 | ||||||
chr11:46773859
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0198 | 2 | NA19056.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2991+2396C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773859 | ||||||
chr11:46773915
|
A | G | 1 | a0005c0015t0001g0287 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2991+2340T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773915 | ||||||
chr11:46773956
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2991+2299G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46773956 | ||||||
chr11:46774351
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2991+1904T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774351 | ||||||
chr11:46774584
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG01243.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2991+1671T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774584 | ||||||
chr11:46774625
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2991+1630A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774625 | ||||||
chr11:46774825
|
T | C | 1 | a0001c0001t0006g0100 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2991+1430A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774825 | ||||||
chr11:46774849
|
T | C | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2991+1406A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774849 | ||||||
chr11:46774884
|
C | A | 1 | a0001c0003t0001g0253 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2991+1371G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774884 | ||||||
chr11:46774897
|
C | G | 1 | a0001c0001t0001g0029 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2991+1358G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774897 | ||||||
chr11:46774962
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2991+1293T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46774962 | ||||||
chr11:46775133
|
A | C | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2991+1122T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775133 | ||||||
chr11:46775138
|
T | A | 1 | a0001c0001t0004g0105 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2991+1117A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775138 | ||||||
chr11:46775431
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2991+824G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775431 | ||||||
chr11:46775592
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2991+663G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775592 | ||||||
chr11:46775671
|
A | AG | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2991+583dupC | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775671 | ||||||
chr11:46775689
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2991+566C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775689 | ||||||
chr11:46775982
|
A | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0179others(1): Show | 4 | NA18941.hp2 NA18970.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.2991+273T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775982 | ||||||
chr11:46775991
|
C | A | 9 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 9 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.2991+264G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 24/43 | chr11 | 46775991 | ||||||
chr11:46776680
|
C | T | 10 | a0001c0002t0003g0120a0001c0002t0003g0121a0001c0002t0003g0122others(7): Show | 10 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2863-297G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46776680 | ||||||
chr11:46776701
|
C | T | 2 | a0001c0004t0002g0047a0001c0004t0002g0085 | 2 | NA18982.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2863-318G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46776701 | ||||||
chr11:46776714
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863-331G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46776714 | ||||||
chr11:46776840
|
T | A | 1 | a0001c0001t0002g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2863-457A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46776840 | ||||||
chr11:46776840
|
T | TATTAA | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.2863-462_2863-458d others(7): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46776840 | ||||||
chr11:46776908
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2863-525G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46776908 | ||||||
chr11:46777081
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(98): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.2862+358T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46777081 | ||||||
chr11:46777129
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2862+310A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 23/43 | chr11 | 46777129 | ||||||
chr11:46777569
|
A | G | 1 | a0001c0003t0001g0203 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2749-17T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 22/43 | chr11 | 46777569 | ||||||
chr11:46777587
|
G | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2749-35C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 22/43 | chr11 | 46777587 | ||||||
chr11:46777623
|
T | A | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2749-71A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 22/43 | chr11 | 46777623 | ||||||
chr11:46777624
|
GC | G | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2749-73delG | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 22/43 | chr11 | 46777624 | ||||||
chr11:46777737
|
T | C | 11 | a0001c0001t0002g0058a0001c0001t0002g0061a0001c0001t0002g0063others(8): Show | 11 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2749-185A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 22/43 | chr11 | 46777737 | ||||||
chr11:46777874
|
C | T | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2748+265G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 22/43 | chr11 | 46777874 | ||||||
chr11:46778428
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG01258.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2573+32A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 21/43 | chr11 | 46778428 | ||||||
chr11:46778799
|
G | A | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2434-200C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46778799 | ||||||
chr11:46778910
|
A | G | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2434-311T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46778910 | ||||||
chr11:46779134
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2434-535T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779134 | ||||||
chr11:46779135
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2434-536A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779135 | ||||||
chr11:46779295
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2434-696C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779295 | ||||||
chr11:46779500
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2433+694T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779500 | ||||||
chr11:46779537
|
C | T | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+657G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779537 | ||||||
chr11:46779538
|
C | G | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+656G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779538 | ||||||
chr11:46779540
|
A | AGT | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+653_2433+654i others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779540 | ||||||
chr11:46779809
|
A | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2433+385T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779809 | ||||||
chr11:46779952
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.2433+242A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46779952 | ||||||
chr11:46780146
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2433+48C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 20/43 | chr11 | 46780146 | ||||||
chr11:46780544
|
C | A | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.2250-59G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46780544 | ||||||
chr11:46780717
|
C | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2250-232G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46780717 | ||||||
chr11:46780750
|
G | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250-265C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46780750 | ||||||
chr11:46781188
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2250-703A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46781188 | ||||||
chr11:46781254
|
T | C | 1 | a0001c0001t0002g0071 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2250-769A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46781254 | ||||||
chr11:46781429
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2250-944A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46781429 | ||||||
chr11:46781429
|
T | TCTC | 286 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.2250-947_2250-945d others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46781429 | ||||||
chr11:46781652
|
C | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2250-1167G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46781652 | ||||||
chr11:46781868
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0003g0218 | 2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2250-1383C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46781868 | ||||||
chr11:46781938
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2249+1336C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46781938 | ||||||
chr11:46782117
|
G | A | 6 | a0001c0002t0003g0004a0001c0002t0003g0262a0001c0002t0003g0264others(3): Show | 7 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2249+1157C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782117 | ||||||
chr11:46782150
|
C | G | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2249+1124G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782150 | ||||||
chr11:46782156
|
C | A | 7 | a0001c0001t0001g0271a0001c0001t0003g0012a0001c0001t0003g0013others(4): Show | 7 | HG02451.hp2 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2249+1118G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782156 | ||||||
chr11:46782158
|
A | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.2249+1116T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782158 | ||||||
chr11:46782160
|
A | C | 17 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0148others(14): Show | 17 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2249+1114T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782160 | ||||||
chr11:46782235
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2249+1039C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782235 | ||||||
chr11:46782379
|
G | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2249+895C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782379 | ||||||
chr11:46782555
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2249+719A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782555 | ||||||
chr11:46782567
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026 | 3 | HG01243.hp2 HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2249+707A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782567 | ||||||
chr11:46782807
|
G | A | 8 | a0001c0002t0003g0004a0001c0002t0003g0262a0001c0002t0003g0263others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2249+467C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782807 | ||||||
chr11:46782826
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2249+448T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782826 | ||||||
chr11:46782838
|
T | C | 1 | a0001c0002t0003g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2249+436A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782838 | ||||||
chr11:46782997
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2249+277A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46782997 | ||||||
chr11:46783019
|
G | A | 1 | a0001c0002t0003g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2249+255C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46783019 | ||||||
chr11:46783033
|
G | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2249+241C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46783033 | ||||||
chr11:46783066
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2249+208G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46783066 | ||||||
chr11:46783121
|
C | A | 1 | a0001c0001t0001g0284 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2249+153G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46783121 | ||||||
chr11:46783211
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2249+63G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 18/43 | chr11 | 46783211 | ||||||
chr11:46783468
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2155-100C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46783468 | ||||||
chr11:46783597
|
GT | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.2155-230delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46783597 | ||||||
chr11:46783699
|
C | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2155-331G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46783699 | ||||||
chr11:46784021
|
A | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | NA18960.hp2 NA18964.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154+467T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784021 | ||||||
chr11:46784025
|
G | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(202): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.2154+463C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784025 | ||||||
chr11:46784096
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2154+392A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784096 | ||||||
chr11:46784123
|
C | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2154+365G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784123 | ||||||
chr11:46784125
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2154+363A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784125 | ||||||
chr11:46784185
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2154+303C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784185 | ||||||
chr11:46784197
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2154+291A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784197 | ||||||
chr11:46784292
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2154+196G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784292 | ||||||
chr11:46784307
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01243.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2154+181C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784307 | ||||||
chr11:46784324
|
T | C | 1 | a0001c0002t0003g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2154+164A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 17/43 | chr11 | 46784324 | ||||||
chr11:46784746
|
T | C | 1 | a0001c0002t0003g0269 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1969-73A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46784746 | ||||||
chr11:46784822
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1969-149T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46784822 | ||||||
chr11:46784872
|
G | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1969-199C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46784872 | ||||||
chr11:46784876
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0219 | 2 | HG00738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1969-203C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46784876 | ||||||
chr11:46785003
|
C | T | 45 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(42): Show | 46 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1969-330G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785003 | ||||||
chr11:46785206
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1969-533C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785206 | ||||||
chr11:46785322
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1969-649A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785322 | ||||||
chr11:46785449
|
G | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1969-776C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785449 | ||||||
chr11:46785672
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1969-999C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785672 | ||||||
chr11:46785714
|
T | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1969-1041A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785714 | ||||||
chr11:46785828
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1969-1155G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785828 | ||||||
chr11:46785987
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1969-1314T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46785987 | ||||||
chr11:46786002
|
A | T | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1969-1329T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786002 | ||||||
chr11:46786038
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1969-1365T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786038 | ||||||
chr11:46786196
|
C | T | 1 | a0001c0002t0003g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1969-1523G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786196 | ||||||
chr11:46786224
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1969-1551A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786224 | ||||||
chr11:46786338
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1969-1665C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786338 | ||||||
chr11:46786596
|
C | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1969-1923G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786596 | ||||||
chr11:46786725
|
C | A | 4 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0208others(1): Show | 4 | HG03654.hp1 NA18955.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1968+1956G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786725 | ||||||
chr11:46786890
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0163a0001c0001t0001g0189others(3): Show | 6 | HG00733.hp1 HG00735.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1968+1791C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786890 | ||||||
chr11:46786922
|
G | A | 1 | a0001c0002t0003g0262 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1968+1759C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46786922 | ||||||
chr11:46787050
|
T | C | 33 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(30): Show | 34 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1968+1631A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787050 | ||||||
chr11:46787240
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1968+1441G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787240 | ||||||
chr11:46787263
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1968+1418T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787263 | ||||||
chr11:46787307
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1968+1374T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787307 | ||||||
chr11:46787370
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1968+1311G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787370 | ||||||
chr11:46787488
|
C | T | 1 | a0001c0002t0003g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1968+1193G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787488 | ||||||
chr11:46787551
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1968+1130A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787551 | ||||||
chr11:46787660
|
A | G | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1968+1021T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787660 | ||||||
chr11:46787697
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1968+984C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787697 | ||||||
chr11:46787785
|
A | T | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1968+896T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787785 | ||||||
chr11:46787832
|
G | A | 44 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(41): Show | 45 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1968+849C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46787832 | ||||||
chr11:46788033
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1968+648G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46788033 | ||||||
chr11:46788316
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1968+365G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46788316 | ||||||
chr11:46788317
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1968+364C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46788317 | ||||||
chr11:46788423
|
A | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1968+258T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46788423 | ||||||
chr11:46788569
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1968+112G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 16/43 | chr11 | 46788569 | ||||||
chr11:46788814
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1876-41C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46788814 | ||||||
chr11:46788891
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1876-118C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46788891 | ||||||
chr11:46789189
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1876-416A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789189 | ||||||
chr11:46789253
|
T | G | 3 | a0001c0001t0001g0240a0001c0007t0001g0233a0001c0007t0001g0234 | 3 | HG02965.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1876-480A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789253 | ||||||
chr11:46789366
|
C | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(50): Show | 54 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1876-593G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789366 | ||||||
chr11:46789624
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1875+452T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789624 | ||||||
chr11:46789656
|
TGTG | T | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1875+417_1875+419d others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789656 | ||||||
chr11:46789688
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1875+388A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789688 | ||||||
chr11:46789733
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1875+343A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789733 | ||||||
chr11:46789787
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1875+289A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789787 | ||||||
chr11:46789970
|
C | G | 2 | a0001c0003t0001g0214a0001c0003t0001g0215 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1875+106G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46789970 | ||||||
chr11:46790016
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1875+60T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 15/43 | chr11 | 46790016 | ||||||
chr11:46790391
|
C | G | 1 | a0001c0001t0002g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1764+79G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 14/43 | chr11 | 46790391 | ||||||
chr11:46790664
|
A | G | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651-81T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46790664 | ||||||
chr11:46790676
|
A | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-93T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46790676 | ||||||
chr11:46790677
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1651-94A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46790677 | ||||||
chr11:46791245
|
GT | G | 76 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(73): Show | 77 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1651-663delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791245 | ||||||
chr11:46791253
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1651-670A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791253 | ||||||
chr11:46791256
|
T | G | 3 | a0001c0001t0001g0109a0001c0006t0005g0288a0001c0006t0008g0289 | 3 | HG02280.hp2 HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-673A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791256 | ||||||
chr11:46791257
|
T | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1651-674A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791257 | ||||||
chr11:46791257
|
T | TG | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(12): Show | 15 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1651-675_1651-674i others(3): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791257 | ||||||
chr11:46791258
|
T | G | 5 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-675A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791258 | ||||||
chr11:46791355
|
GCCTCCCA others(11): Show |
G | 32 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(29): Show | 32 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1651-790_1651-773d others(20): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791355 | ||||||
chr11:46791531
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1651-948T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791531 | ||||||
chr11:46791568
|
G | A | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-985C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791568 | ||||||
chr11:46791581
|
G | T | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1651-998C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791581 | ||||||
chr11:46791937
|
C | T | 8 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG02896.hp1 HG03098.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-1354G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791937 | ||||||
chr11:46791998
|
A | C | 6 | a0001c0001t0001g0180a0001c0001t0001g0197a0001c0001t0001g0198others(3): Show | 6 | HG00438.hp2 NA18947.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651-1415T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46791998 | ||||||
chr11:46792191
|
C | A | 1 | a0001c0001t0001g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1651-1608G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792191 | ||||||
chr11:46792205
|
T | TCTC | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1651-1623_1651-162 others(7): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792205 | ||||||
chr11:46792210
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0168 | 3 | HG01934.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1651-1627A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792210 | ||||||
chr11:46792552
|
C | CA | 27 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(24): Show | 28 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1651-1970dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792552 | ||||||
chr11:46792552
|
C | CAA | 10 | a0001c0002t0003g0120a0001c0002t0003g0121a0001c0002t0003g0122others(7): Show | 10 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1651-1971_1651-197 others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792552 | ||||||
chr11:46792565
|
AAACAAC | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-1988_1651-198 others(10): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792565 | ||||||
chr11:46792573
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1651-1990T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792573 | ||||||
chr11:46792649
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-2066C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792649 | ||||||
chr11:46792769
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1651-2186T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792769 | ||||||
chr11:46792772
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-2189C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792772 | ||||||
chr11:46792786
|
G | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-2203C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792786 | ||||||
chr11:46792819
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-2236T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792819 | ||||||
chr11:46792857
|
G | A | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1651-2274C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46792857 | ||||||
chr11:46793146
|
T | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1650+2448A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793146 | ||||||
chr11:46793188
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1650+2406T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793188 | ||||||
chr11:46793235
|
A | G | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1650+2359T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793235 | ||||||
chr11:46793294
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1650+2300A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793294 | ||||||
chr11:46793416
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1650+2178T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793416 | ||||||
chr11:46793651
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1650+1943T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793651 | ||||||
chr11:46793740
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1650+1854G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793740 | ||||||
chr11:46793902
|
G | A | 9 | a0001c0001t0002g0069a0001c0004t0002g0047a0001c0004t0002g0084others(6): Show | 9 | HG00597.hp1 NA18967.hp1 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650+1692C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793902 | ||||||
chr11:46793935
|
C | CA | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1650+1658dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793935 | ||||||
chr11:46793975
|
A | AT | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1650+1618dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793975 | ||||||
chr11:46793998
|
G | A | 1 | a0001c0001t0006g0100 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1650+1596C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46793998 | ||||||
chr11:46794055
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1650+1539G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794055 | ||||||
chr11:46794083
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(50): Show | 54 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1650+1511G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794083 | ||||||
chr11:46794286
|
T | A | 1 | a0001c0002t0003g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1650+1308A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794286 | ||||||
chr11:46794471
|
A | G | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1650+1123T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794471 | ||||||
chr11:46794474
|
G | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | NA18960.hp2 NA18964.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1650+1120C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794474 | ||||||
chr11:46794503
|
CAAG | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(98): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1650+1088_1650+109 others(7): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794503 | ||||||
chr11:46794566
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1650+1028C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794566 | ||||||
chr11:46794690
|
G | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0168 | 3 | HG01934.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1650+904C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794690 | ||||||
chr11:46794704
|
C | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1650+890G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46794704 | ||||||
chr11:46795120
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1650+474C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46795120 | ||||||
chr11:46795121
|
G | A | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1650+473C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46795121 | ||||||
chr11:46795154
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1650+440A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46795154 | ||||||
chr11:46795259
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1650+335G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46795259 | ||||||
chr11:46795327
|
C | CA | 77 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(74): Show | 78 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1650+266dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46795327 | ||||||
chr11:46795412
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1650+182A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46795412 | ||||||
chr11:46795573
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1650+21T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 13/43 | chr11 | 46795573 | ||||||
chr11:46796065
|
T | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1468-289A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796065 | ||||||
chr11:46796160
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1468-384A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796160 | ||||||
chr11:46796164
|
CA | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 146 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.1468-389delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796164 | ||||||
chr11:46796164
|
CAAAAAAA others(1): Show |
C | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1468-396_1468-389d others(10): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796164 | ||||||
chr11:46796365
|
T | C | 1 | a0001c0002t0003g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1467+447A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796365 | ||||||
chr11:46796444
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1467+368C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796444 | ||||||
chr11:46796493
|
A | T | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1467+319T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796493 | ||||||
chr11:46796516
|
T | TA | 14 | a0001c0002t0003g0118a0001c0002t0003g0119a0001c0002t0003g0125others(11): Show | 14 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1467+295dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796516 | ||||||
chr11:46796531
|
G | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0152a0001c0001t0001g0162others(2): Show | 5 | HG01934.hp2 HG01975.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1467+281C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796531 | ||||||
chr11:46796548
|
G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1467+264C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796548 | ||||||
chr11:46796661
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1467+151A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 12/43 | chr11 | 46796661 | ||||||
chr11:46796974
|
G | A | 2 | a0001c0002t0003g0135a0001c0002t0003g0138 | 2 | HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1339-34C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46796974 | ||||||
chr11:46797081
|
T | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0151a0001c0001t0001g0173others(1): Show | 4 | HG01071.hp2 HG01515.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1339-141A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797081 | ||||||
chr11:46797227
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1339-287G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797227 | ||||||
chr11:46797264
|
G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1339-324C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797264 | ||||||
chr11:46797320
|
T | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1339-380A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797320 | ||||||
chr11:46797390
|
C | CA | 38 | a0001c0001t0001g0256a0001c0002t0003g0004a0001c0002t0003g0118others(35): Show | 39 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1338+414dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797390 | ||||||
chr11:46797392
|
A | AC | 77 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(74): Show | 78 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1338+412_1338+413i others(3): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797392 | ||||||
chr11:46797393
|
A | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1338+412T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797393 | ||||||
chr11:46797396
|
A | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0267 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1338+409T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797396 | ||||||
chr11:46797472
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1338+333T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 11/43 | chr11 | 46797472 | ||||||
chr11:46798494
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1084-322A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46798494 | ||||||
chr11:46798530
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1084-358G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46798530 | ||||||
chr11:46798541
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1084-369G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46798541 | ||||||
chr11:46798583
|
A | C | 1 | a0001c0001t0002g0090 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1084-411T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46798583 | ||||||
chr11:46798789
|
A | G | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1084-617T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46798789 | ||||||
chr11:46799163
|
AT | A | 14 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0188others(11): Show | 14 | HG00609.hp1 HG03654.hp1 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1084-992delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799163 | ||||||
chr11:46799233
|
G | A | 3 | a0001c0002t0003g0132a0001c0002t0003g0139a0001c0013t0003g0131 | 3 | HG00735.hp1 HG01257.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1084-1061C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799233 | ||||||
chr11:46799238
|
G | A | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(30): Show | 33 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1084-1066C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799238 | ||||||
chr11:46799267
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0010g0290a0003c0009t0001g0241 | 3 | HG00738.hp2 HG01358.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1084-1095C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799267 | ||||||
chr11:46799277
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1084-1105A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799277 | ||||||
chr11:46799318
|
A | C | 1 | a0001c0002t0003g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1084-1146T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799318 | ||||||
chr11:46799349
|
A | G | 44 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(41): Show | 45 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1084-1177T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799349 | ||||||
chr11:46799528
|
A | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1084-1356T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799528 | ||||||
chr11:46799560
|
T | C | 1 | a0001c0002t0003g0139 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1084-1388A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799560 | ||||||
chr11:46799570
|
T | C | 6 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0049others(3): Show | 7 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.1084-1398A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799570 | ||||||
chr11:46799921
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1083+1279G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799921 | ||||||
chr11:46799938
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1083+1262G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46799938 | ||||||
chr11:46800047
|
G | A | 1 | a0001c0002t0003g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1083+1153C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800047 | ||||||
chr11:46800115
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1083+1085A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800115 | ||||||
chr11:46800293
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0196 | 3 | HG01243.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1083+907A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800293 | ||||||
chr11:46800453
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1083+747A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800453 | ||||||
chr11:46800519
|
T | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0192 | 2 | NA18973.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1083+681A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800519 | ||||||
chr11:46800528
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1083+672A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800528 | ||||||
chr11:46800536
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0249 | 3 | HG02630.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1083+664C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800536 | ||||||
chr11:46800619
|
T | TTA | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1083+579_1083+580d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800619 | ||||||
chr11:46800687
|
C | A | 1 | a0001c0001t0001g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1083+513G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800687 | ||||||
chr11:46800690
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1083+510A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800690 | ||||||
chr11:46800767
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1083+433T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800767 | ||||||
chr11:46800981
|
CCTGA | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(71): Show | 75 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1083+215_1083+218d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800981 | ||||||
chr11:46800991
|
T | C | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1083+209A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46800991 | ||||||
chr11:46801071
|
A | C | 1 | a0001c0001t0002g0090 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1083+129T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46801071 | ||||||
chr11:46801136
|
C | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1083+64G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 9/43 | chr11 | 46801136 | ||||||
chr11:46801367
|
T | C | 2 | a0001c0003t0001g0214a0001c0003t0001g0215 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.979-63A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46801367 | ||||||
chr11:46801497
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979-193G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46801497 | ||||||
chr11:46801560
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979-256A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46801560 | ||||||
chr11:46801633
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.979-329C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46801633 | ||||||
chr11:46802103
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979-799G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802103 | ||||||
chr11:46802131
|
T | C | 26 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(23): Show | 26 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.979-827A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802131 | ||||||
chr11:46802166
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0177 | 2 | HG01071.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.979-862C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802166 | ||||||
chr11:46802253
|
G | C | 1 | a0001c0001t0002g0059 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.979-949C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802253 | ||||||
chr11:46802307
|
C | T | 9 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 9 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.979-1003G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802307 | ||||||
chr11:46802315
|
G | A | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-1011C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802315 | ||||||
chr11:46802392
|
T | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.979-1088A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802392 | ||||||
chr11:46802395
|
T | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0210a0001c0001t0001g0211others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.979-1091A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802395 | ||||||
chr11:46802480
|
GTTGCAGT others(23): Show |
G | 2 | a0001c0002t0003g0124a0001c0002t0003g0141 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.979-1206_979-1177d others(32): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802480 | ||||||
chr11:46802531
|
AAGAC | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(24): Show | 27 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.979-1231_979-1228d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802531 | ||||||
chr11:46802549
|
G | GACAC | 3 | a0001c0002t0003g0132a0001c0002t0003g0139a0001c0013t0003g0131 | 3 | HG00735.hp1 HG01257.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.979-1246_979-1245i others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802549 | ||||||
chr11:46802553
|
G | C | 4 | a0001c0001t0002g0038a0001c0002t0003g0132a0001c0002t0003g0139others(1): Show | 4 | HG00735.hp1 HG01257.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-1249C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GAC | 16 | a0001c0001t0001g0109a0001c0001t0002g0022a0001c0001t0002g0050others(13): Show | 16 | HG01074.hp1 HG01975.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.979-1251_979-1250d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GACAC | 16 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(13): Show | 16 | HG01109.hp1 HG02615.hp1 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.979-1250_979-1249i others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GACACAC | 3 | a0001c0001t0002g0078a0001c0001t0002g0091a0001c0002t0003g0121 | 3 | HG00438.hp1 HG01074.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.979-1250_979-1249i others(8): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GACACACA others(1): Show |
4 | a0001c0002t0003g0120a0001c0002t0003g0122a0001c0002t0003g0124others(1): Show | 4 | HG01515.hp1 HG01981.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-1250_979-1249i others(10): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GACACACA others(3): Show |
2 | a0001c0002t0003g0123a0001c0002t0003g0141 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.979-1250_979-1249i others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GAGACACA others(1): Show |
21 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(18): Show | 22 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.979-1250_979-1249i others(10): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GAGACACA others(3): Show |
1 | a0001c0002t0003g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.979-1250_979-1249i others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802553
|
G | GAGACACA others(9): Show |
1 | a0001c0002t0003g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.979-1250_979-1249i others(18): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802553 | ||||||
chr11:46802557
|
G | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(236): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.979-1253C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802557 | ||||||
chr11:46802557
|
G | GAC | 3 | a0001c0001t0002g0102a0001c0001t0007g0011a0001c0008t0003g0108 | 3 | HG02965.hp1 HG02976.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.979-1255_979-1254d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802557 | ||||||
chr11:46802557
|
G | GACACAC | 6 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1259_979-1254d others(8): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802557 | ||||||
chr11:46802557
|
G | GACACACA others(7): Show |
3 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274 | 3 | HG02280.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.979-1267_979-1254d others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802557 | ||||||
chr11:46802557
|
G | GACACACA others(9): Show |
1 | a0001c0002t0003g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.979-1269_979-1254d others(18): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802557 | ||||||
chr11:46802557
|
G | GACAGAC | 3 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.979-1254_979-1253i others(8): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802557 | ||||||
chr11:46802561
|
C | G | 1 | a0001c0001t0002g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.979-1257G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802561 | ||||||
chr11:46802563
|
C | CACAT | 28 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(25): Show | 28 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-1260_979-1259i others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802563 | ||||||
chr11:46802563
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.979-1259G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802563 | ||||||
chr11:46802618
|
C | T | 1 | a0001c0002t0003g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.979-1314G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802618 | ||||||
chr11:46802691
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.979-1387C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802691 | ||||||
chr11:46802722
|
T | C | 9 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-1418A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802722 | ||||||
chr11:46802815
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-1511A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802815 | ||||||
chr11:46802850
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979-1546C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46802850 | ||||||
chr11:46803055
|
G | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-1751C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803055 | ||||||
chr11:46803140
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.979-1836A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803140 | ||||||
chr11:46803196
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979-1892C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803196 | ||||||
chr11:46803357
|
C | G | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.979-2053G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803357 | ||||||
chr11:46803396
|
C | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979-2092G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803396 | ||||||
chr11:46803398
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979-2094C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803398 | ||||||
chr11:46803410
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979-2106T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803410 | ||||||
chr11:46803433
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.979-2129T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803433 | ||||||
chr11:46803766
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0003g0218 | 2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.979-2462A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803766 | ||||||
chr11:46803840
|
T | C | 2 | a0001c0002t0003g0119a0001c0002t0003g0133 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.979-2536A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803840 | ||||||
chr11:46803978
|
C | T | 6 | a0001c0002t0003g0004a0001c0002t0003g0262a0001c0002t0003g0264others(3): Show | 7 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-2674G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46803978 | ||||||
chr11:46804041
|
G | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-2737C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46804041 | ||||||
chr11:46804228
|
A | T | 2 | a0001c0003t0001g0214a0001c0003t0001g0215 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.979-2924T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46804228 | ||||||
chr11:46804492
|
T | C | 1 | a0001c0002t0003g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.979-3188A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46804492 | ||||||
chr11:46804540
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | NA18951.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.979-3236A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46804540 | ||||||
chr11:46804560
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.979-3256T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46804560 | ||||||
chr11:46804917
|
G | C | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.978+3114C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46804917 | ||||||
chr11:46805131
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.978+2900G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805131 | ||||||
chr11:46805132
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+2899C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805132 | ||||||
chr11:46805159
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+2872G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805159 | ||||||
chr11:46805227
|
T | C | 1 | a0001c0003t0001g0209 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.978+2804A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805227 | ||||||
chr11:46805341
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.978+2690A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805341 | ||||||
chr11:46805517
|
TCTTTTTT others(19): Show |
T | 1 | a0001c0001t0001g0280 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.978+2488_978+2513d others(28): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805517 | ||||||
chr11:46805607
|
G | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+2424C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805607 | ||||||
chr11:46805617
|
A | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2414T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805617 | ||||||
chr11:46805764
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+2267G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805764 | ||||||
chr11:46805807
|
G | C | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.978+2224C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805807 | ||||||
chr11:46805819
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.978+2212G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46805819 | ||||||
chr11:46806118
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+1913G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46806118 | ||||||
chr11:46806252
|
C | T | 1 | a0001c0002t0003g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.978+1779G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46806252 | ||||||
chr11:46806406
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+1625G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46806406 | ||||||
chr11:46806520
|
G | A | 2 | a0001c0001t0002g0060a0001c0001t0002g0080 | 2 | NA18747.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.978+1511C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46806520 | ||||||
chr11:46806692
|
T | C | 1 | a0001c0002t0003g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.978+1339A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46806692 | ||||||
chr11:46806712
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+1319G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46806712 | ||||||
chr11:46806723
|
T | C | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.978+1308A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46806723 | ||||||
chr11:46807109
|
T | C | 1 | a0001c0002t0003g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.978+922A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807109 | ||||||
chr11:46807249
|
A | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.978+782T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807249 | ||||||
chr11:46807291
|
G | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+740C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807291 | ||||||
chr11:46807334
|
G | A | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.978+697C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807334 | ||||||
chr11:46807345
|
A | G | 44 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(41): Show | 45 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.978+686T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807345 | ||||||
chr11:46807370
|
T | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+661A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807370 | ||||||
chr11:46807427
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+604T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807427 | ||||||
chr11:46807434
|
T | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+597A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807434 | ||||||
chr11:46807624
|
T | A | 39 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(36): Show | 40 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.978+407A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807624 | ||||||
chr11:46807884
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+147T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 8/43 | chr11 | 46807884 | ||||||
chr11:46808174
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.865-30G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808174 | ||||||
chr11:46808243
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.865-99A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808243 | ||||||
chr11:46808263
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.865-119G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808263 | ||||||
chr11:46808327
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.865-183C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808327 | ||||||
chr11:46808352
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.865-208A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808352 | ||||||
chr11:46808353
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.865-209T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808353 | ||||||
chr11:46808535
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0050 | 2 | HG00558.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.865-391G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808535 | ||||||
chr11:46808573
|
T | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(2): Show | 5 | HG00438.hp2 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.865-429A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808573 | ||||||
chr11:46808630
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.865-486T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808630 | ||||||
chr11:46808665
|
A | G | 3 | a0001c0001t0002g0017a0001c0001t0002g0048a0001c0004t0002g0047 | 3 | NA18982.hp2 NA18989.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.865-521T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808665 | ||||||
chr11:46808830
|
G | A | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+570C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46808830 | ||||||
chr11:46809023
|
C | G | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+377G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46809023 | ||||||
chr11:46809025
|
T | C | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.864+375A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46809025 | ||||||
chr11:46809106
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+294G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46809106 | ||||||
chr11:46809209
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.864+191T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46809209 | ||||||
chr11:46809297
|
G | A | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.864+103C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 7/43 | chr11 | 46809297 | ||||||
chr11:46809578
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.764-78G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 6/43 | chr11 | 46809578 | ||||||
chr11:46809975
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.631-101G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46809975 | ||||||
chr11:46810088
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.631-214G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810088 | ||||||
chr11:46810262
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.631-388C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810262 | ||||||
chr11:46810315
|
G | GATTC | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0184 | 3 | HG00741.hp1 HG01167.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.631-445_631-442dup others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810315 | ||||||
chr11:46810387
|
C | T | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-513G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810387 | ||||||
chr11:46810605
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.630+402G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810605 | ||||||
chr11:46810608
|
C | A | 26 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(23): Show | 26 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.630+399G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810608 | ||||||
chr11:46810644
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.630+363G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810644 | ||||||
chr11:46810692
|
T | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+315A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810692 | ||||||
chr11:46810767
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.630+240A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810767 | ||||||
chr11:46810811
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.630+196T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810811 | ||||||
chr11:46810815
|
T | C | 1 | a0001c0003t0001g0204 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.630+192A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810815 | ||||||
chr11:46810942
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.630+65G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 5/43 | chr11 | 46810942 | ||||||
chr11:46811477
|
C | G | 1 | a0001c0001t0003g0015 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459-299G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46811477 | ||||||
chr11:46811542
|
T | C | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.459-364A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46811542 | ||||||
chr11:46811624
|
G | A | 5 | a0001c0001t0004g0077a0001c0001t0004g0105a0001c0001t0004g0107others(2): Show | 5 | NA18949.hp2 NA18973.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-446C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46811624 | ||||||
chr11:46811659
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.459-481A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46811659 | ||||||
chr11:46811717
|
T | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.459-539A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46811717 | ||||||
chr11:46811755
|
C | T | 6 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG01109.hp1 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-577G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46811755 | ||||||
chr11:46812082
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0052 | 2 | HG02080.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.459-904C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812082 | ||||||
chr11:46812203
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.459-1025G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812203 | ||||||
chr11:46812324
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-1146C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812324 | ||||||
chr11:46812329
|
C | T | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-1151G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812329 | ||||||
chr11:46812346
|
A | T | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.459-1168T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812346 | ||||||
chr11:46812486
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-1308A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812486 | ||||||
chr11:46812618
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.459-1440T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812618 | ||||||
chr11:46812648
|
C | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.459-1470G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812648 | ||||||
chr11:46812701
|
G | A | 10 | a0001c0002t0003g0120a0001c0002t0003g0121a0001c0002t0003g0122others(7): Show | 10 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.459-1523C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812701 | ||||||
chr11:46812722
|
C | T | 1 | a0001c0003t0001g0205 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.459-1544G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812722 | ||||||
chr11:46812723
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-1545C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812723 | ||||||
chr11:46812798
|
C | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.459-1620G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812798 | ||||||
chr11:46812952
|
A | C | 1 | a0001c0001t0002g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.459-1774T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46812952 | ||||||
chr11:46813075
|
T | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.459-1897A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46813075 | ||||||
chr11:46813512
|
C | T | 2 | a0001c0005t0001g0032a0001c0005t0001g0033 | 2 | NA18960.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.459-2334G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46813512 | ||||||
chr11:46814063
|
C | T | 1 | a0005c0015t0001g0287 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.458+2135G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814063 | ||||||
chr11:46814131
|
C | CA | 7 | a0001c0001t0002g0055a0001c0001t0002g0072a0001c0001t0002g0097others(4): Show | 7 | HG00621.hp1 HG02145.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.458+2066dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814131 | ||||||
chr11:46814131
|
CAA | C | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 58 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.458+2065_458+2066d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814131 | ||||||
chr11:46814131
|
CAAA | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.458+2064_458+2066d others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814131 | ||||||
chr11:46814346
|
T | C | 2 | a0001c0001t0002g0078a0001c0001t0002g0091 | 2 | HG00438.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.458+1852A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814346 | ||||||
chr11:46814533
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.458+1665T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814533 | ||||||
chr11:46814551
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.458+1647C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814551 | ||||||
chr11:46814615
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.458+1583G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814615 | ||||||
chr11:46814687
|
T | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.458+1511A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814687 | ||||||
chr11:46814784
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.458+1414A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46814784 | ||||||
chr11:46815061
|
T | C | 34 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(31): Show | 34 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.458+1137A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815061 | ||||||
chr11:46815197
|
T | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(74): Show | 78 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.458+1001A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815197 | ||||||
chr11:46815236
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.458+962T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815236 | ||||||
chr11:46815545
|
ACT | A | 10 | a0001c0002t0003g0120a0001c0002t0003g0121a0001c0002t0003g0122others(7): Show | 10 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.458+651_458+652del others(2): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815545 | ||||||
chr11:46815618
|
G | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.458+580C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815618 | ||||||
chr11:46815649
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.458+549T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815649 | ||||||
chr11:46815651
|
T | C | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.458+547A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815651 | ||||||
chr11:46815667
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.458+531A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815667 | ||||||
chr11:46815941
|
C | A | 6 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0179others(3): Show | 6 | NA18941.hp2 NA18967.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.458+257G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46815941 | ||||||
chr11:46816007
|
T | C | 23 | a0001c0001t0001g0150a0001c0001t0001g0210a0001c0001t0001g0211others(20): Show | 23 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.458+191A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46816007 | ||||||
chr11:46816075
|
AC | A | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.458+122delG | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 4/43 | chr11 | 46816075 | ||||||
chr11:46816460
|
G | C | 1 | a0001c0003t0001g0203 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.252-56C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816460 | ||||||
chr11:46816601
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.252-197A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816601 | ||||||
chr11:46816685
|
A | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0169 | 2 | NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.252-281T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816685 | ||||||
chr11:46816702
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.252-298G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816702 | ||||||
chr11:46816786
|
A | AT | 11 | a0001c0003t0001g0203a0001c0003t0001g0205a0001c0003t0001g0206others(8): Show | 11 | HG00609.hp1 HG02896.hp1 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.252-383dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816786 | ||||||
chr11:46816786
|
AT | A | 111 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0150others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.252-383delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816786 | ||||||
chr11:46816786
|
ATT | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(137): Show | 142 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.252-384_252-383del others(2): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816786 | ||||||
chr11:46816786
|
ATTT | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0041others(11): Show | 14 | HG01070.hp1 HG01167.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.252-385_252-383del others(3): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816786 | ||||||
chr11:46816918
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252-514G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816918 | ||||||
chr11:46816997
|
T | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252-593A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46816997 | ||||||
chr11:46817060
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.252-656G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817060 | ||||||
chr11:46817087
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.252-683G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817087 | ||||||
chr11:46817094
|
G | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-690C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817094 | ||||||
chr11:46817206
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252-802G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817206 | ||||||
chr11:46817287
|
T | A | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-883A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817287 | ||||||
chr11:46817386
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.251+924T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817386 | ||||||
chr11:46817856
|
A | T | 1 | a0001c0001t0002g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.251+454T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817856 | ||||||
chr11:46817917
|
T | C | 1 | a0001c0002t0003g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.251+393A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817917 | ||||||
chr11:46817985
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.251+325C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46817985 | ||||||
chr11:46818231
|
A | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+79T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 3/43 | chr11 | 46818231 | ||||||
chr11:46818568
|
TG | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.58-66delC | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46818568 | ||||||
chr11:46818644
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.58-141A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46818644 | ||||||
chr11:46818853
|
G | A | 1 | a0001c0002t0003g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-350C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46818853 | ||||||
chr11:46819278
|
C | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-775G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46819278 | ||||||
chr11:46819376
|
T | C | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58-873A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46819376 | ||||||
chr11:46819639
|
A | C | 2 | a0001c0003t0001g0214a0001c0003t0001g0215 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58-1136T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46819639 | ||||||
chr11:46819640
|
G | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.58-1137C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46819640 | ||||||
chr11:46819929
|
G | A | 1 | a0001c0003t0001g0204 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.57+1246C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46819929 | ||||||
chr11:46820213
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.57+962G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46820213 | ||||||
chr11:46820384
|
A | G | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.57+791T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46820384 | ||||||
chr11:46820386
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.57+789A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46820386 | ||||||
chr11:46820494
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.57+681G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46820494 | ||||||
chr11:46820718
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.57+457T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46820718 | ||||||
chr11:46820819
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.57+356G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46820819 | ||||||
chr11:46820903
|
C | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.57+272G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46820903 | ||||||
chr11:46821085
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.57+90A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 2/43 | chr11 | 46821085 | ||||||
chr11:46821290
|
C | A | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-37-22G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821290 | ||||||
chr11:46821421
|
C | CT | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(138): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-37-154dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821421 | ||||||
chr11:46821421
|
C | CTT | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 92 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-37-155_-37-154dup others(2): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821421 | ||||||
chr11:46821421
|
C | CTTT | 36 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(33): Show | 36 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.-37-156_-37-154dup others(3): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821421 | ||||||
chr11:46821421
|
C | CTTTT | 8 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG00438.hp2 NA18906.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-157_-37-154dup others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821421 | ||||||
chr11:46821486
|
C | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-37-218G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821486 | ||||||
chr11:46821504
|
A | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-236T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821504 | ||||||
chr11:46821525
|
C | T | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-37-257G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821525 | ||||||
chr11:46821671
|
C | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | NA18747.hp2 NA18954.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-403G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821671 | ||||||
chr11:46821761
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-493G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821761 | ||||||
chr11:46821795
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-37-527A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821795 | ||||||
chr11:46821795
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-37-527A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821795 | ||||||
chr11:46821807
|
G | A | 2 | a0001c0003t0001g0214a0001c0003t0001g0215 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-37-539C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821807 | ||||||
chr11:46821823
|
G | C | 1 | a0001c0002t0003g0262 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-37-555C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821823 | ||||||
chr11:46821961
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-37-693G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46821961 | ||||||
chr11:46822026
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-37-758T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822026 | ||||||
chr11:46822548
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0002g0114 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-37-1280C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822548 | ||||||
chr11:46822740
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-1472G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822740 | ||||||
chr11:46822741
|
C | CA | 6 | a0001c0001t0002g0040a0001c0001t0002g0091a0001c0001t0002g0098others(3): Show | 6 | HG03225.hp1 NA18979.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-1474dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822741 | ||||||
chr11:46822741
|
CA | C | 229 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-37-1474delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822741 | ||||||
chr11:46822742
|
A | C | 3 | a0001c0002t0003g0133a0001c0002t0003g0142a0001c0002t0003g0286 | 3 | HG02145.hp2 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-37-1474T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822742 | ||||||
chr11:46822743
|
A | C | 20 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(17): Show | 21 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.-37-1475T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822743 | ||||||
chr11:46822744
|
A | C | 1 | a0001c0002t0003g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-37-1476T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822744 | ||||||
chr11:46822761
|
A | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-37-1493T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822761 | ||||||
chr11:46822803
|
A | G | 7 | a0001c0001t0001g0109a0001c0001t0001g0277a0001c0001t0001g0282others(4): Show | 7 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-1535T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822803 | ||||||
chr11:46822820
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-37-1552A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46822820 | ||||||
chr11:46823112
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-1844T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823112 | ||||||
chr11:46823137
|
A | C | 2 | a0001c0001t0002g0035a0001c0001t0002g0050 | 2 | HG00558.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-37-1869T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823137 | ||||||
chr11:46823215
|
A | C | 1 | a0001c0001t0003g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-37-1947T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823215 | ||||||
chr11:46823298
|
C | T | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-37-2030G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823298 | ||||||
chr11:46823409
|
A | G | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-2141T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823409 | ||||||
chr11:46823663
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-2395A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823663 | ||||||
chr11:46823675
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-2407A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823675 | ||||||
chr11:46823716
|
G | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-2448C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823716 | ||||||
chr11:46823766
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-2498T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823766 | ||||||
chr11:46823796
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-37-2528A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823796 | ||||||
chr11:46823870
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-2602C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46823870 | ||||||
chr11:46824032
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-2764A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46824032 | ||||||
chr11:46824076
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-37-2808T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46824076 | ||||||
chr11:46824134
|
T | C | 13 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(10): Show | 13 | HG00609.hp1 HG01496.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37-2866A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46824134 | ||||||
chr11:46824263
|
C | T | 1 | a0001c0013t0003g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-37-2995G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46824263 | ||||||
chr11:46824300
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0249 | 3 | HG02630.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-37-3032C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46824300 | ||||||
chr11:46824802
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-3534T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46824802 | ||||||
chr11:46825058
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-3790A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46825058 | ||||||
chr11:46825728
|
A | G | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 54 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.-37-4460T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46825728 | ||||||
chr11:46825753
|
T | TA | 17 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0210others(14): Show | 17 | HG00738.hp2 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37-4486dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46825753 | ||||||
chr11:46825899
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-37-4631A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46825899 | ||||||
chr11:46826068
|
G | T | 2 | a0001c0001t0002g0095a0001c0001t0002g0101 | 2 | HG02132.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-37-4800C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46826068 | ||||||
chr11:46826164
|
G | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-37-4896C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46826164 | ||||||
chr11:46826257
|
A | T | 1 | a0001c0001t0002g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-37-4989T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46826257 | ||||||
chr11:46826467
|
T | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | NA18960.hp2 NA18964.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-5199A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46826467 | ||||||
chr11:46826774
|
G | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-5506C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46826774 | ||||||
chr11:46826904
|
G | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-5636C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46826904 | ||||||
chr11:46826922
|
G | A | 1 | a0005c0015t0001g0287 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-37-5654C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46826922 | ||||||
chr11:46827243
|
T | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-5975A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46827243 | ||||||
chr11:46827611
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-37-6343T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46827611 | ||||||
chr11:46827701
|
G | A | 1 | a0001c0014t0001g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-37-6433C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46827701 | ||||||
chr11:46827808
|
C | T | 1 | a0001c0002t0003g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-37-6540G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46827808 | ||||||
chr11:46827809
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-37-6541C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46827809 | ||||||
chr11:46828035
|
G | A | 1 | a0001c0002t0003g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-37-6767C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828035 | ||||||
chr11:46828345
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-7077G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828345 | ||||||
chr11:46828403
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-7135T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828403 | ||||||
chr11:46828497
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-37-7229G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828497 | ||||||
chr11:46828533
|
G | C | 1 | a0001c0003t0001g0253 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-37-7265C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828533 | ||||||
chr11:46828641
|
T | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-7373A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828641 | ||||||
chr11:46828646
|
CAAT | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-7381_-37-7379d others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828646 | ||||||
chr11:46828828
|
A | G | 1 | a0001c0001t0001g0031 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-37-7560T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828828 | ||||||
chr11:46828936
|
A | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-7668T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46828936 | ||||||
chr11:46829272
|
A | G | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-8004T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829272 | ||||||
chr11:46829282
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-37-8014A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829282 | ||||||
chr11:46829437
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-37-8169G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829437 | ||||||
chr11:46829438
|
G | A | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-37-8170C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829438 | ||||||
chr11:46829504
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-8236G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829504 | ||||||
chr11:46829513
|
C | A | 13 | a0001c0002t0003g0118a0001c0002t0003g0119a0001c0002t0003g0127others(10): Show | 13 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-37-8245G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829513 | ||||||
chr11:46829834
|
TTGTA | T | 3 | a0001c0002t0003g0122a0001c0002t0003g0123a0001c0002t0003g0141 | 3 | HG01515.hp1 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-37-8570_-37-8567d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829834 | ||||||
chr11:46829834
|
TTGTATG | T | 3 | a0001c0002t0003g0120a0001c0002t0003g0121a0001c0002t0003g0132 | 3 | HG00735.hp1 HG01074.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-37-8572_-37-8567d others(8): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829834 | ||||||
chr11:46829838
|
A | ATG | 8 | a0001c0001t0002g0049a0001c0001t0002g0063a0001c0001t0002g0064others(5): Show | 8 | HG01099.hp2 HG01993.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-8572_-37-8571d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
A | G | 2 | a0001c0002t0003g0124a0001c0002t0003g0137 | 2 | HG02257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-37-8570T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
ATG | A | 16 | a0001c0001t0001g0176a0001c0001t0002g0081a0001c0001t0002g0082others(13): Show | 16 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37-8572_-37-8571d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
ATGTG | A | 14 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0258others(11): Show | 14 | HG01192.hp2 HG02132.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-37-8574_-37-8571d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
ATGTGTG | A | 11 | a0001c0001t0001g0178a0001c0001t0001g0230a0001c0001t0001g0239others(8): Show | 11 | HG01070.hp1 HG01081.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-8576_-37-8571d others(8): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
ATGTGTGT others(1): Show |
A | 34 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0028others(31): Show | 34 | HG00642.hp2 HG00673.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.-37-8578_-37-8571d others(10): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
ATGTGTGT others(3): Show |
A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(103): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-37-8580_-37-8571d others(12): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
ATGTGTGT others(5): Show |
A | 8 | a0001c0001t0001g0240a0001c0001t0001g0277a0001c0001t0001g0282others(5): Show | 8 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-8582_-37-8571d others(14): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829838
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-37-8586_-37-8571d others(18): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829838 | ||||||
chr11:46829875
|
T | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-8607A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829875 | ||||||
chr11:46829908
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-37-8640G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46829908 | ||||||
chr11:46830111
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-37-8843T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830111 | ||||||
chr11:46830112
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-37-8844A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830112 | ||||||
chr11:46830164
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-37-8896C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830164 | ||||||
chr11:46830169
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-8901G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830169 | ||||||
chr11:46830197
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-37-8929A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830197 | ||||||
chr11:46830297
|
C | T | 3 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0015 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-37-9029G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830297 | ||||||
chr11:46830374
|
G | C | 1 | a0001c0001t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-37-9106C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830374 | ||||||
chr11:46830440
|
C | CA | 34 | a0001c0001t0002g0022a0001c0001t0002g0036a0001c0002t0003g0004others(31): Show | 35 | HG00735.hp1 HG01109.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.-37-9173dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830440 | ||||||
chr11:46830440
|
C | CAA | 77 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0002g0001others(74): Show | 78 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-37-9174_-37-9173d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830440 | ||||||
chr11:46830440
|
CA | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-37-9173delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830440 | ||||||
chr11:46830566
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-37-9298C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830566 | ||||||
chr11:46830643
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-37-9375C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830643 | ||||||
chr11:46830786
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-37-9518C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830786 | ||||||
chr11:46830791
|
G | A | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-37-9523C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830791 | ||||||
chr11:46830917
|
T | C | 4 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-9649A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46830917 | ||||||
chr11:46831051
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-9783A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831051 | ||||||
chr11:46831202
|
T | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-37-9934A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831202 | ||||||
chr11:46831288
|
A | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(71): Show | 75 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-37-10020T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831288 | ||||||
chr11:46831324
|
C | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-10056G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831324 | ||||||
chr11:46831374
|
T | G | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-37-10106A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831374 | ||||||
chr11:46831531
|
C | T | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-37-10263G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831531 | ||||||
chr11:46831861
|
C | CT | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-37-10594dupA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831861 | ||||||
chr11:46831861
|
C | CTT | 12 | a0001c0001t0001g0145a0001c0001t0001g0153a0001c0001t0001g0222others(9): Show | 12 | HG01515.hp2 HG01978.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-10595_-37-1059 others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831861 | ||||||
chr11:46831861
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-37-10593G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831861 | ||||||
chr11:46831915
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-37-10647G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831915 | ||||||
chr11:46831926
|
A | C | 1 | a0001c0004t0002g0047 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-37-10658T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831926 | ||||||
chr11:46831978
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37-10710G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46831978 | ||||||
chr11:46832547
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-11279T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46832547 | ||||||
chr11:46832841
|
C | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-37-11573G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46832841 | ||||||
chr11:46832969
|
A | T | 1 | a0001c0003t0001g0204 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-37-11701T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46832969 | ||||||
chr11:46833223
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-11955T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833223 | ||||||
chr11:46833329
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-12061T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833329 | ||||||
chr11:46833381
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0261 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-37-12113C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833381 | ||||||
chr11:46833426
|
C | T | 43 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(40): Show | 44 | HG00735.hp1 HG01074.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-37-12158G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833426 | ||||||
chr11:46833467
|
T | C | 9 | a0001c0004t0002g0084a0001c0004t0002g0085a0001c0004t0002g0086others(6): Show | 9 | HG00597.hp1 NA18967.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-12199A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833467 | ||||||
chr11:46833493
|
G | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-37-12225C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833493 | ||||||
chr11:46833548
|
G | A | 1 | a0001c0002t0003g0130 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-12280C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833548 | ||||||
chr11:46833572
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-37-12304C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833572 | ||||||
chr11:46833579
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37-12311G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833579 | ||||||
chr11:46833682
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-12414G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833682 | ||||||
chr11:46833857
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-38+12363A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833857 | ||||||
chr11:46833970
|
A | C | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | NA18747.hp2 NA18954.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+12250T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46833970 | ||||||
chr11:46834153
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-38+12067G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834153 | ||||||
chr11:46834162
|
T | C | 4 | a0001c0001t0002g0056a0001c0001t0002g0059a0001c0001t0002g0089others(1): Show | 4 | NA18971.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+12058A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834162 | ||||||
chr11:46834450
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-38+11770G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834450 | ||||||
chr11:46834453
|
T | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+11767A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834453 | ||||||
chr11:46834462
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38+11758A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834462 | ||||||
chr11:46834519
|
C | CA | 15 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0041others(12): Show | 16 | HG00673.hp1 HG01934.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-38+11700dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834519 | ||||||
chr11:46834519
|
CA | C | 92 | a0001c0001t0001g0007a0001c0001t0001g0109a0001c0001t0001g0112others(89): Show | 93 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-38+11700delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834519 | ||||||
chr11:46834784
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-38+11436T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834784 | ||||||
chr11:46834832
|
G | T | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-38+11388C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834832 | ||||||
chr11:46834919
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+11301G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834919 | ||||||
chr11:46834971
|
AT | A | 118 | a0001c0001t0001g0258a0001c0001t0001g0282a0001c0001t0001g0283others(115): Show | 120 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.-38+11248delA | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834971 | ||||||
chr11:46834985
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(98): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.-38+11235A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46834985 | ||||||
chr11:46835042
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-38+11178C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835042 | ||||||
chr11:46835142
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+11078A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835142 | ||||||
chr11:46835236
|
A | T | 2 | a0001c0007t0001g0233a0001c0007t0001g0234 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-38+10984T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835236 | ||||||
chr11:46835394
|
A | G | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+10826T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835394 | ||||||
chr11:46835449
|
T | C | 1 | a0001c0002t0003g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-38+10771A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835449 | ||||||
chr11:46835450
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-38+10770T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835450 | ||||||
chr11:46835475
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-38+10745A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835475 | ||||||
chr11:46835508
|
C | T | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38+10712G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835508 | ||||||
chr11:46835573
|
C | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+10647G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835573 | ||||||
chr11:46835728
|
T | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(75): Show | 79 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-38+10492A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835728 | ||||||
chr11:46835953
|
T | C | 31 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(28): Show | 31 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-38+10267A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46835953 | ||||||
chr11:46836039
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+10181T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836039 | ||||||
chr11:46836046
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | NA19056.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-38+10174A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836046 | ||||||
chr11:46836238
|
T | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+9982A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836238 | ||||||
chr11:46836255
|
G | T | 1 | a0001c0002t0003g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-38+9965C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836255 | ||||||
chr11:46836263
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-38+9957C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836263 | ||||||
chr11:46836335
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+9885C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836335 | ||||||
chr11:46836396
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38+9824C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836396 | ||||||
chr11:46836615
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+9605T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46836615 | ||||||
chr11:46837280
|
G | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0059a0001c0001t0002g0089others(1): Show | 4 | NA18971.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+8940C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837280 | ||||||
chr11:46837306
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-38+8914G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837306 | ||||||
chr11:46837332
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-38+8888G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837332 | ||||||
chr11:46837379
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-38+8841A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837379 | ||||||
chr11:46837422
|
A | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(30): Show | 33 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-38+8798T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837422 | ||||||
chr11:46837524
|
A | C | 1 | a0001c0001t0001g0003 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-38+8696T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837524 | ||||||
chr11:46837570
|
T | C | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38+8650A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837570 | ||||||
chr11:46837686
|
CAT | C | 6 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0244others(3): Show | 6 | HG00733.hp2 HG01070.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+8532_-38+8533d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837686 | ||||||
chr11:46837805
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+8415T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837805 | ||||||
chr11:46837874
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-38+8346T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46837874 | ||||||
chr11:46838014
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-38+8206A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838014 | ||||||
chr11:46838067
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0249 | 3 | HG02630.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-38+8153A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838067 | ||||||
chr11:46838177
|
T | C | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+8043A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838177 | ||||||
chr11:46838215
|
C | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38+8005G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838215 | ||||||
chr11:46838236
|
T | A | 35 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(32): Show | 35 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+7984A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838236 | ||||||
chr11:46838237
|
A | T | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+7983T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838237 | ||||||
chr11:46838316
|
G | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01167.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-38+7904C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838316 | ||||||
chr11:46838415
|
T | C | 1 | a0001c0001t0006g0100 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-38+7805A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838415 | ||||||
chr11:46838445
|
T | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+7775A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838445 | ||||||
chr11:46838505
|
G | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+7715C>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838505 | ||||||
chr11:46838546
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+7674G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838546 | ||||||
chr11:46838596
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-38+7624G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838596 | ||||||
chr11:46838602
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+7618T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838602 | ||||||
chr11:46838617
|
CA | C | 15 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0193others(12): Show | 15 | HG01071.hp2 HG01192.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+7602delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838617 | ||||||
chr11:46838617
|
CAA | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(123): Show | 128 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-38+7601_-38+7602d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838617 | ||||||
chr11:46838617
|
CAAA | C | 139 | a0001c0001t0001g0041a0001c0001t0001g0109a0001c0001t0001g0145others(136): Show | 141 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-38+7600_-38+7602d others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838617 | ||||||
chr11:46838617
|
CAAAA | C | 6 | a0001c0001t0001g0232a0001c0001t0002g0045a0001c0001t0002g0060others(3): Show | 6 | HG00733.hp2 HG01070.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+7599_-38+7602d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838617 | ||||||
chr11:46838653
|
G | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+7567C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838653 | ||||||
chr11:46838793
|
C | CA | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(184): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-38+7426dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838793 | ||||||
chr11:46838793
|
C | CAA | 68 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 69 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-38+7425_-38+7426d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838793 | ||||||
chr11:46838793
|
C | CAAA | 11 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0201others(8): Show | 11 | HG00438.hp2 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+7424_-38+7426d others(5): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838793 | ||||||
chr11:46838793
|
C | CAAAA | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+7423_-38+7426d others(6): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46838793 | ||||||
chr11:46839199
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-38+7021A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839199 | ||||||
chr11:46839209
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0271 | 2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-38+7011C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839209 | ||||||
chr11:46839259
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-38+6961C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839259 | ||||||
chr11:46839304
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-38+6916G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839304 | ||||||
chr11:46839449
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-38+6771A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839449 | ||||||
chr11:46839609
|
G | A | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+6611C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839609 | ||||||
chr11:46839657
|
T | C | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+6563A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839657 | ||||||
chr11:46839860
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-38+6360C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839860 | ||||||
chr11:46839863
|
A | G | 286 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-38+6357T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839863 | ||||||
chr11:46839893
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+6327T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839893 | ||||||
chr11:46839922
|
T | C | 1 | a0001c0001t0006g0100 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-38+6298A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46839922 | ||||||
chr11:46840126
|
A | C | 1 | a0001c0001t0001g0250 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-38+6094T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840126 | ||||||
chr11:46840281
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-38+5939A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840281 | ||||||
chr11:46840503
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+5717G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840503 | ||||||
chr11:46840512
|
C | G | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38+5708G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840512 | ||||||
chr11:46840513
|
T | G | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38+5707A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840513 | ||||||
chr11:46840521
|
T | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(282): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-38+5699A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840521 | ||||||
chr11:46840707
|
C | T | 1 | a0001c0003t0001g0203 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-38+5513G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840707 | ||||||
chr11:46840832
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+5388T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840832 | ||||||
chr11:46840985
|
T | C | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+5235A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46840985 | ||||||
chr11:46841098
|
G | A | 2 | a0001c0001t0003g0111a0001c0001t0007g0011 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-38+5122C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841098 | ||||||
chr11:46841232
|
C | T | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-38+4988G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841232 | ||||||
chr11:46841267
|
C | CA | 13 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(10): Show | 13 | HG00438.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-38+4952dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841267 | ||||||
chr11:46841331
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-38+4889G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841331 | ||||||
chr11:46841459
|
G | A | 1 | a0001c0001t0002g0101 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-38+4761C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841459 | ||||||
chr11:46841607
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-38+4613T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841607 | ||||||
chr11:46841684
|
G | T | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-38+4536C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841684 | ||||||
chr11:46841940
|
G | A | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+4280C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841940 | ||||||
chr11:46841944
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-38+4276C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841944 | ||||||
chr11:46841986
|
A | C | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+4234T>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841986 | ||||||
chr11:46841997
|
C | CA | 106 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0261others(103): Show | 108 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-38+4222dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841997 | ||||||
chr11:46841997
|
C | CAA | 8 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(5): Show | 8 | HG00597.hp1 HG02258.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+4221_-38+4222d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841997 | ||||||
chr11:46841997
|
CA | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 70 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.-38+4222delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841997 | ||||||
chr11:46841997
|
CAA | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(75): Show | 80 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-38+4221_-38+4222d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46841997 | ||||||
chr11:46842085
|
G | T | 1 | a0001c0008t0003g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38+4135C>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46842085 | ||||||
chr11:46842267
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+3953G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46842267 | ||||||
chr11:46842966
|
C | CA | 37 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38+3253dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46842966 | ||||||
chr11:46842966
|
C | CAA | 8 | a0001c0001t0001g0261a0001c0002t0003g0139a0001c0002t0003g0140others(5): Show | 8 | HG01257.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38+3252_-38+3253d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46842966 | ||||||
chr11:46842966
|
CA | C | 74 | a0001c0001t0001g0144a0001c0001t0002g0001a0001c0001t0002g0017others(71): Show | 75 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-38+3253delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46842966 | ||||||
chr11:46842966
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0143 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-38+3240_-38+3253d others(16): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46842966 | ||||||
chr11:46843154
|
T | C | 37 | a0001c0002t0003g0004a0001c0002t0003g0118a0001c0002t0003g0119others(34): Show | 38 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38+3066A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843154 | ||||||
chr11:46843245
|
C | T | 7 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+2975G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843245 | ||||||
chr11:46843304
|
C | T | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+2916G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843304 | ||||||
chr11:46843449
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-38+2771C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843449 | ||||||
chr11:46843552
|
A | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+2668T>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843552 | ||||||
chr11:46843635
|
T | C | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+2585A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843635 | ||||||
chr11:46843657
|
G | A | 3 | a0001c0003t0001g0251a0001c0003t0001g0252a0001c0003t0001g0253 | 3 | HG00609.hp1 NA18971.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-38+2563C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843657 | ||||||
chr11:46843683
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-38+2537A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843683 | ||||||
chr11:46843708
|
C | T | 14 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0035others(11): Show | 15 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+2512G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843708 | ||||||
chr11:46843709
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-38+2511C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843709 | ||||||
chr11:46843728
|
GA | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-38+2491delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843728 | ||||||
chr11:46843728
|
GAA | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(7): Show | 10 | HG00558.hp1 HG00642.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+2490_-38+2491d others(4): Show |
CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843728 | ||||||
chr11:46843892
|
C | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | NA18960.hp2 NA18964.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+2328G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46843892 | ||||||
chr11:46844221
|
T | TA | 18 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(15): Show | 19 | HG01109.hp2 HG01884.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.-38+1998dupT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844221 | ||||||
chr11:46844221
|
TA | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+1998delT | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844221 | ||||||
chr11:46844379
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01243.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-38+1841G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844379 | ||||||
chr11:46844588
|
A | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-38+1632T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844588 | ||||||
chr11:46844646
|
T | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+1574A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844646 | ||||||
chr11:46844844
|
C | G | 1 | a0001c0001t0002g0017 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-38+1376G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844844 | ||||||
chr11:46844866
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-38+1354C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844866 | ||||||
chr11:46844971
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-38+1249T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46844971 | ||||||
chr11:46845224
|
G | A | 4 | a0001c0002t0003g0272a0001c0002t0003g0273a0001c0002t0003g0274others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+996C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845224 | ||||||
chr11:46845270
|
C | A | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+950G>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845270 | ||||||
chr11:46845394
|
T | C | 1 | a0002c0012t0001g0276 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38+826A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845394 | ||||||
chr11:46845470
|
C | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(282): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-38+750G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845470 | ||||||
chr11:46845537
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-38+683A>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845537 | ||||||
chr11:46845599
|
T | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | NA18967.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-38+621A>G | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845599 | ||||||
chr11:46845640
|
A | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-38+580T>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845640 | ||||||
chr11:46845651
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-38+569C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845651 | ||||||
chr11:46845653
|
C | T | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0014others(2): Show | 5 | HG02723.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+567G>A | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845653 | ||||||
chr11:46845806
|
C | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+414G>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845806 | ||||||
chr11:46845817
|
G | A | 1 | a0001c0002t0003g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+403C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46845817 | ||||||
chr11:46846019
|
G | A | 1 | a0005c0015t0001g0287 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-38+201C>T | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46846019 | ||||||
chr11:46846109
|
T | G | 2 | a0001c0006t0005g0288a0001c0006t0008g0289 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+111A>C | CKAP5 | ENSG00000175216.15 | transcript | ENST00000529230.6 | protein_coding | 1/43 | chr11 | 46846109 |