geneid | 22995 |
---|---|
ensemblid | ENSG00000103995.14 |
hgncid | 29298 |
symbol | CEP152 |
name | centrosomal protein 152 |
refseq_nuc | NM_001194998.2 |
refseq_prot | NP_001181927.1 |
ensembl_nuc | ENST00000380950.7 |
ensembl_prot | ENSP00000370337.2 |
mane_status | MANE Select |
chr | chr15 |
start | 48737938 |
end | 48811069 |
strand | - |
ver | v1.2 |
region | chr15:48737938-48811069 |
region5000 | chr15:48732938-48816069 |
regionname0 | CEP152_chr15_48737938_48811069 |
regionname5000 | CEP152_chr15_48732938_48816069 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1710 | 220 | 59 | 36 | 81 | 14 | 28 | 64 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002 | 0/0 | 1710 | 44 | 0 | 5 | 32 | 0 | 7 | 24 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0003 | 0/0 | 1710 | 27 | 0 | 4 | 23 | 0 | 0 | 19 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0004 | 0/0 | 1710 | 16 | 1 | 1 | 14 | 0 | 0 | 9 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0005 | 0/0 | 1710 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0006 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0007 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0008 | 0/0 | 1710 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0009 | 0/0 | 1710 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0010 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0011 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0012 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0013 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0014 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0015 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0016 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0017 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0018 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0019 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0020 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0021 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0022 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0023 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0024 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0025 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0026 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0027 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0028 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0029 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 5133 | 211 | 55 | 36 | 77 | 13 | 28 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0002 | 0/0 | 5133 | 42 | 0 | 5 | 31 | 0 | 6 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0003 | 0/0 | 5133 | 27 | 0 | 4 | 23 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0004 | 0/0 | 5133 | 16 | 1 | 1 | 14 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0005 | 0/0 | 5133 | 4 | 4 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0006 | 0/0 | 5133 | 3 | 3 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0007 | 0/0 | 5133 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0008 | 0/0 | 5133 | 2 | 0 | 0 | 0 | 0 | 2 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0009 | 0/0 | 5133 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0010 | 0/0 | 5133 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0011 | 0/0 | 5133 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0012 | 0/0 | 5133 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0013 | 0/0 | 5133 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0014 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0015 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0016 | 0/0 | 5133 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0017 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0018 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0019 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0020 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0021 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0022 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0023 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0024 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0025 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0026 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0027 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0028 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0029 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0030 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0031 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0032 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0033 | 0/0 | 5133 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0034 | 0/0 | 5133 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0035 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0036 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0037 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0038 | 0/0 | 5133 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
c0039 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 428 | 235 | 65 | 32 | 103 | 12 | 21 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
t0002 | 0/0 | 428 | 89 | 9 | 10 | 58 | 1 | 11 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
t0003 | 0/0 | 428 | 9 | 0 | 4 | 0 | 0 | 5 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
t0004 | 0/0 | 428 | 5 | 2 | 2 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
t0005 | 0/0 | 428 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
t0006 | 0/0 | 428 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
t0007 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0009 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5133 | 211 | 55 | 36 | 77 | 13 | 28 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0007 | 0/0 | 5133 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0009 | 0/0 | 5133 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0014 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0016 | 0/0 | 5133 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0023 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0024 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0036 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002c0002 | 0/0 | 5133 | 42 | 0 | 5 | 31 | 0 | 6 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002c0037 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002c0038 | 0/0 | 5133 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0003c0003 | 0/0 | 5133 | 27 | 0 | 4 | 23 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0004c0004 | 0/0 | 5133 | 16 | 1 | 1 | 14 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0005c0005 | 0/0 | 5133 | 4 | 4 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0006c0012 | 0/0 | 5133 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0006c0017 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0007c0006 | 0/0 | 5133 | 3 | 3 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0008c0008 | 0/0 | 5133 | 2 | 0 | 0 | 0 | 0 | 2 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0009c0010 | 0/0 | 5133 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0010c0011 | 0/0 | 5133 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0011c0039 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0012c0013 | 0/0 | 5133 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0013c0035 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0014c0034 | 0/0 | 5133 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0015c0029 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0016c0030 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0017c0028 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0018c0025 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0019c0022 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0020c0021 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0021c0026 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0022c0020 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0023c0019 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0024c0018 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0025c0027 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0026c0032 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0027c0031 | 0/0 | 5133 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0028c0033 | 0/0 | 5133 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0029c0015 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5560 | 158 | 45 | 25 | 56 | 12 | 18 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0001t0002 | 0/0 | 5560 | 40 | 8 | 5 | 21 | 1 | 5 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0001t0003 | 0/0 | 5560 | 9 | 0 | 4 | 0 | 0 | 5 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0001t0004 | 0/0 | 5560 | 4 | 2 | 2 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0007t0001 | 0/0 | 5560 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0009t0005 | 0/0 | 5560 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0014t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0016t0004 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0023t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0024t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0001c0036t0002 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002c0002t0002 | 0/0 | 5560 | 41 | 0 | 5 | 31 | 0 | 5 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002c0002t0006 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002c0037t0007 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0002c0038t0002 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0003c0003t0001 | 0/0 | 5560 | 24 | 0 | 4 | 20 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0003c0003t0002 | 0/0 | 5560 | 3 | 0 | 0 | 3 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0004c0004t0001 | 0/0 | 5560 | 16 | 1 | 1 | 14 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0005c0005t0001 | 0/0 | 5560 | 4 | 4 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0006c0012t0001 | 0/0 | 5560 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0006c0017t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0007c0006t0001 | 0/0 | 5560 | 3 | 3 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0008c0008t0001 | 0/0 | 5560 | 2 | 0 | 0 | 0 | 0 | 2 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0009c0010t0001 | 0/0 | 5560 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0010c0011t0001 | 0/0 | 5560 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0011c0039t0002 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0012c0013t0001 | 0/0 | 5560 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0013c0035t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0014c0034t0001 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0015c0029t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0016c0030t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0017c0028t0002 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0018c0025t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0019c0022t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0020c0021t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0021c0026t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0022c0020t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0023c0019t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0024c0018t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0025c0027t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0026c0032t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0027c0031t0002 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0028c0033t0001 | 0/0 | 5560 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
a0029c0015t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | copy fasta | chr15 | 48732938 | 48816069 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0009 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0007t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0007t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0009t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0009t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0014t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0016t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0023t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0024t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0036t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0037t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0038t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0006c0012t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0006c0012t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0006c0017t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0007c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0007c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0007c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0008c0008t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0008c0008t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0009c0010t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0009c0010t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0010c0011t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0010c0011t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0011c0039t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0012c0013t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0013c0035t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0014c0034t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0015c0029t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0016c0030t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0017c0028t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0018c0025t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0019c0022t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0020c0021t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0021c0026t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0022c0020t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0023c0019t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0024c0018t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0025c0027t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0026c0032t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0027c0031t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0028c0033t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0029c0015t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00099 | hp2 | a0001 | c0016 | t0004 | g0110 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0317 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00558 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00597 | hp2 | a0029 | c0015 | t0001 | g0142 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00735 | hp2 | a0003 | c0003 | t0001 | g0154 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0248 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01081 | hp2 | a0012 | c0013 | t0001 | g0081 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01106 | hp1 | a0028 | c0033 | t0001 | g0113 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0282 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01255 | hp2 | a0004 | c0004 | t0001 | g0145 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0264 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01884 | hp1 | a0024 | c0018 | t0001 | g0232 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01884 | hp2 | a0007 | c0006 | t0001 | g0018 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01891 | hp1 | a0027 | c0031 | t0002 | g0321 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0156 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0158 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02027 | hp2 | a0015 | c0029 | t0001 | g0166 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02040 | hp2 | a0004 | c0004 | t0001 | g0051 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02056 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02056 | hp2 | a0004 | c0004 | t0001 | g0039 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02074 | hp2 | a0011 | c0039 | t0002 | g0256 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02080 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02129 | hp1 | a0025 | c0027 | t0001 | g0182 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02132 | hp2 | a0004 | c0004 | t0001 | g0144 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02257 | hp2 | a0006 | c0012 | t0001 | g0057 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02258 | hp1 | a0001 | c0024 | t0001 | g0138 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02451 | hp1 | a0018 | c0025 | t0001 | g0231 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0254 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02622 | hp1 | a0020 | c0021 | t0001 | g0137 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02630 | hp1 | a0001 | c0009 | t0005 | g0022 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02630 | hp2 | a0005 | c0005 | t0001 | g0044 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02647 | hp1 | a0004 | c0004 | t0001 | g0055 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02717 | hp2 | a0010 | c0011 | t0001 | g0096 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03017 | hp1 | a0002 | c0038 | t0002 | g0266 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03041 | hp1 | a0006 | c0012 | t0001 | g0077 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03041 | hp2 | a0021 | c0026 | t0001 | g0131 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03130 | hp2 | a0005 | c0005 | t0001 | g0052 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03209 | hp1 | a0007 | c0006 | t0001 | g0026 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03225 | hp1 | a0005 | c0005 | t0001 | g0053 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03225 | hp2 | a0006 | c0017 | t0001 | g0025 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03453 | hp1 | a0007 | c0006 | t0001 | g0019 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03491 | hp1 | a0002 | c0002 | t0006 | g0265 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03491 | hp2 | a0014 | c0034 | t0001 | g0128 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03516 | hp1 | a0010 | c0011 | t0001 | g0097 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03540 | hp1 | a0001 | c0009 | t0005 | g0023 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03831 | hp1 | a0008 | c0008 | t0001 | g0189 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0268 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04184 | hp1 | a0008 | c0008 | t0001 | g0126 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0250 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0259 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18612 | hp1 | a0004 | c0004 | t0001 | g0170 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18906 | hp2 | a0005 | c0005 | t0001 | g0050 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0297 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18943 | hp1 | a0013 | c0035 | t0001 | g0071 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18949 | hp1 | a0004 | c0004 | t0001 | g0141 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0168 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18956 | hp2 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0211 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18963 | hp1 | a0004 | c0004 | t0001 | g0095 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18963 | hp2 | a0003 | c0003 | t0002 | g0295 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18965 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0208 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18968 | hp2 | a0004 | c0004 | t0001 | g0151 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18975 | hp1 | a0001 | c0007 | t0001 | g0218 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18981 | hp1 | a0009 | c0010 | t0001 | g0061 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18985 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18988 | hp1 | a0002 | c0037 | t0007 | g0327 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18992 | hp1 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18993 | hp1 | a0022 | c0020 | t0001 | g0069 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18993 | hp2 | a0004 | c0004 | t0001 | g0147 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0227 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19000 | hp1 | a0026 | c0032 | t0001 | g0149 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19002 | hp1 | a0003 | c0003 | t0002 | g0285 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19030 | hp1 | a0023 | c0019 | t0001 | g0111 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19058 | hp2 | a0004 | c0004 | t0001 | g0146 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19059 | hp2 | a0004 | c0004 | t0001 | g0171 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19060 | hp2 | a0017 | c0028 | t0002 | g0287 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19076 | hp2 | a0001 | c0007 | t0001 | g0183 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19079 | hp1 | a0001 | c0014 | t0001 | g0181 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19080 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19084 | hp1 | a0009 | c0010 | t0001 | g0073 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19087 | hp1 | a0016 | c0030 | t0001 | g0207 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19087 | hp2 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19089 | hp1 | a0001 | c0036 | t0002 | g0311 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19089 | hp2 | a0004 | c0004 | t0001 | g0150 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ASW | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ASW | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG06807 | hp2 | a0001 | c0023 | t0001 | g0118 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18955 | hp2 | a0019 | c0022 | t0001 | g0046 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0009 | REF | REF | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0125 | REF | REF | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48738304
|
G | A | 1 | a0008 | 2 | HG03831.hp1 HG04184.hp1 |
missense_variant | MODERATE | c.5078C>T | p.Pro1693Leu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5194/5560 | 5078/5133 | 1693/1710 | chr15 | 48738304 | ||
chr15:48738625
|
C | G | 1 | a0015 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.4757G>C | p.Arg1586Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4873/5560 | 4757/5133 | 1586/1710 | chr15 | 48738625 | ||
chr15:48739207
|
A | G | 1 | a0019 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.4175T>C | p.Ile1392Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4291/5560 | 4175/5133 | 1392/1710 | chr15 | 48739207 | ||
chr15:48741607
|
G | A | 1 | a0018 | 1 | HG02451.hp1 | stop_gained | HIGH | c.4087C>T | p.Gln1363* | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/27 | 4203/5560 | 4087/5133 | 1363/1710 | chr15 | 48741607 | ||
chr15:48741617
|
G | C | 1 | a0021 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.4077C>G | p.Ser1359Arg | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/27 | 4193/5560 | 4077/5133 | 1359/1710 | chr15 | 48741617 | ||
chr15:48742014
|
C | T | 1 | a0020 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3922G>A | p.Ala1308Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 25/27 | 4038/5560 | 3922/5133 | 1308/1710 | chr15 | 48742014 | ||
chr15:48744900
|
G | C | 1 | a0016 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.3727C>G | p.Pro1243Ala | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/27 | 3843/5560 | 3727/5133 | 1243/1710 | chr15 | 48744900 | ||
chr15:48744915
|
G | C | 1 | a0021 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3712C>G | p.Leu1238Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/27 | 3828/5560 | 3712/5133 | 1238/1710 | chr15 | 48744915 | ||
chr15:48748540
|
C | G | 1 | a0005 | 4 | HG02630.hp2 HG03130.hp2 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.3537G>C | p.Lys1179Asn | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/27 | 3653/5560 | 3537/5133 | 1179/1710 | chr15 | 48748540 | ||
chr15:48752382
|
G | T | 1 | a0022 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.3433C>A | p.Pro1145Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/27 | 3549/5560 | 3433/5133 | 1145/1710 | chr15 | 48752382 | ||
chr15:48752460
|
C | T | 1 | a0023 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.3355G>A | p.Ala1119Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/27 | 3471/5560 | 3355/5133 | 1119/1710 | chr15 | 48752460 | ||
chr15:48755923
|
C | G | 1 | a0024 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.3325G>C | p.Ala1109Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 3441/5560 | 3325/5133 | 1109/1710 | chr15 | 48755923 | ||
chr15:48755931
|
A | G | 2 | a0006a0010 | 5 | HG02257.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.3317T>C | p.Val1106Ala | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 3433/5560 | 3317/5133 | 1106/1710 | chr15 | 48755931 | ||
chr15:48755970
|
C | T | 1 | a0007 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.3278G>A | p.Cys1093Tyr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 3394/5560 | 3278/5133 | 1093/1710 | chr15 | 48755970 | ||
chr15:48756379
|
G | A | 1 | a0016 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.2869C>T | p.Arg957Trp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2985/5560 | 2869/5133 | 957/1710 | chr15 | 48756379 | ||
chr15:48756444
|
T | C | 1 | a0025 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.2804A>G | p.Gln935Arg | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2920/5560 | 2804/5133 | 935/1710 | chr15 | 48756444 | ||
chr15:48756471
|
T | A | 1 | a0009 | 2 | NA18981.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.2777A>T | p.Glu926Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2893/5560 | 2777/5133 | 926/1710 | chr15 | 48756471 | ||
chr15:48756508
|
G | C | 1 | a0004 | 16 | HG00558.hp2 HG01255.hp2 HG02040.hp2 others(13): Show |
missense_variant | MODERATE | c.2740C>G | p.Leu914Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2856/5560 | 2740/5133 | 914/1710 | chr15 | 48756508 | ||
chr15:48760148
|
G | A | 2 | a0017a0026 | 2 | NA19000.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.2681C>T | p.Ser894Phe | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/27 | 2797/5560 | 2681/5133 | 894/1710 | chr15 | 48760148 | ||
chr15:48762575
|
C | A | 4 | a0003a0011a0015others(1): Show | 30 | HG00735.hp2 HG01981.hp2 HG02004.hp1 others(27): Show |
missense_variant | MODERATE | c.2378G>T | p.Ser793Ile | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/27 | 2494/5560 | 2378/5133 | 793/1710 | chr15 | 48762575 | ||
chr15:48762612
|
T | C | 2 | a0026a0027 | 2 | HG01891.hp1 NA19000.hp1 |
missense_variant | MODERATE | c.2341A>G | p.Ile781Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/27 | 2457/5560 | 2341/5133 | 781/1710 | chr15 | 48762612 | ||
chr15:48767136
|
T | C | 1 | a0028 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.2204A>G | p.Glu735Gly | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/27 | 2320/5560 | 2204/5133 | 735/1710 | chr15 | 48767136 | ||
chr15:48768237
|
T | C | 1 | a0010 | 2 | HG02717.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2000A>G | p.Lys667Arg | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/27 | 2116/5560 | 2000/5133 | 667/1710 | chr15 | 48768237 | ||
chr15:48784063
|
C | G | 1 | a0029 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1231G>C | p.Ala411Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/27 | 1347/5560 | 1231/5133 | 411/1710 | chr15 | 48784063 | ||
chr15:48788836
|
T | C | 1 | a0014 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1138A>G | p.Asn380Asp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/27 | 1254/5560 | 1138/5133 | 380/1710 | chr15 | 48788836 | ||
chr15:48793394
|
C | A | 1 | a0013 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.759G>T | p.Glu253Asp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/27 | 875/5560 | 759/5133 | 253/1710 | chr15 | 48793394 | ||
chr15:48797497
|
C | T | 1 | a0012 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.344G>A | p.Arg115Gln | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/27 | 460/5560 | 344/5133 | 115/1710 | chr15 | 48797497 | ||
chr15:48797978
|
G | A | 2 | a0002a0011 | 45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
missense_variant | MODERATE | c.161C>T | p.Ser54Leu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/27 | 277/5560 | 161/5133 | 54/1710 | chr15 | 48797978 | ||
chr15:48810963
|
G | C | 1 | a0002 | 1 | NA18988.hp1 | splice_region_variant | LOW | c.-10C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | chr15 | 48810963 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48738267
|
T | C | 1 | a0001c0024 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.5115A>G | p.Pro1705Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5231/5560 | 5115/5133 | 1705/1710 | chr15 | 48738267 | ||
chr15:48738303
|
C | T | 1 | a0002c0038 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.5079G>A | p.Pro1693Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5195/5560 | 5079/5133 | 1693/1710 | chr15 | 48738303 | ||
chr15:48738468
|
T | C | 1 | a0001c0009 | 2 | HG02630.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.4914A>G | p.Pro1638Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5030/5560 | 4914/5133 | 1638/1710 | chr15 | 48738468 | ||
chr15:48738510
|
A | G | 1 | a0002c0037 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.4872T>C | p.Asn1624Asn | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4988/5560 | 4872/5133 | 1624/1710 | chr15 | 48738510 | ||
chr15:48738525
|
A | G | 2 | a0001c0024a0024c0018 | 2 | HG01884.hp1 HG02258.hp1 |
synonymous_variant | LOW | c.4857T>C | p.Asp1619Asp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4973/5560 | 4857/5133 | 1619/1710 | chr15 | 48738525 | ||
chr15:48738909
|
C | G | 1 | a0001c0023 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.4473G>C | p.Pro1491Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4589/5560 | 4473/5133 | 1491/1710 | chr15 | 48738909 | ||
chr15:48739083
|
A | G | 1 | a0010c0011 | 2 | HG02717.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.4299T>C | p.His1433His | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4415/5560 | 4299/5133 | 1433/1710 | chr15 | 48739083 | ||
chr15:48752386
|
A | C | 1 | a0001c0007 | 2 | NA18975.hp1 NA19076.hp2 |
synonymous_variant | LOW | c.3429T>G | p.Ala1143Ala | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/27 | 3545/5560 | 3429/5133 | 1143/1710 | chr15 | 48752386 | ||
chr15:48767078
|
C | T | 1 | a0001c0016 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.2262G>A | p.Glu754Glu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/27 | 2378/5560 | 2262/5133 | 754/1710 | chr15 | 48767078 | ||
chr15:48768998
|
C | A | 1 | a0006c0012 | 2 | HG02257.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.1866G>T | p.Leu622Leu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/27 | 1982/5560 | 1866/5133 | 622/1710 | chr15 | 48768998 | ||
chr15:48796104
|
C | T | 1 | a0001c0014 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.597G>A | p.Gln199Gln | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/27 | 713/5560 | 597/5133 | 199/1710 | chr15 | 48796104 | ||
chr15:48797541
|
T | C | 1 | a0001c0036 | 1 | NA19089.hp1 | synonymous_variant | LOW | c.300A>G | p.Lys100Lys | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/27 | 416/5560 | 300/5133 | 100/1710 | chr15 | 48797541 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48738055
|
C | T | 1 | a0001c0009t0005 | 2 | HG02630.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*194G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 194 | chr15 | 48738055 | |||||
chr15:48738079
|
A | G | 2 | a0001c0001t0004a0001c0016t0004 | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*170T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 170 | chr15 | 48738079 | |||||
chr15:48738244
|
C | A | 1 | a0002c0002t0006 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5 | chr15 | 48738244 | |||||
chr15:48810977
|
T | A | 1 | a0001c0001t0003 | 9 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | chr15 | 48810977 | ||||||
chr15:48810978
|
G | T | 1 | a0001c0001t0003 | 9 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-25C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | 5329 | chr15 | 48810978 | |||||
chr15:48810979
|
T | A | 1 | a0001c0001t0003 | 9 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-26A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | 5330 | chr15 | 48810979 | |||||
chr15:48811047
|
T | C | 10 | a0001c0001t0002a0001c0036t0002a0002c0002t0002others(7): Show | 91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-94A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | 5398 | chr15 | 48811047 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48739297
|
T | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4094-9A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739297 | ||||||
chr15:48739342
|
G | A | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4094-54C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739342 | ||||||
chr15:48739364
|
TA | T | 5 | a0006c0012t0001g0057a0006c0012t0001g0077a0006c0017t0001g0025others(2): Show | 5 | HG02257.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-77delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739364 | ||||||
chr15:48739811
|
A | G | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4094-523T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739811 | ||||||
chr15:48739940
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4094-652G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739940 | ||||||
chr15:48740168
|
C | G | 1 | a0002c0002t0002g0267 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.4094-880G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740168 | ||||||
chr15:48740211
|
T | C | 2 | a0021c0026t0001g0131a0027c0031t0002g0321 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4094-923A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740211 | ||||||
chr15:48740502
|
C | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 316 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.4093+1099G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740502 | ||||||
chr15:48740588
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4093+1013C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740588 | ||||||
chr15:48740615
|
C | CT | 86 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0038others(83): Show | 91 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.4093+985dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740615 | ||||||
chr15:48740615
|
C | CTT | 13 | a0001c0001t0001g0029a0001c0001t0001g0101a0001c0001t0001g0140others(10): Show | 13 | HG01952.hp1 HG02717.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.4093+984_4093+985d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740615 | ||||||
chr15:48740615
|
CT | C | 10 | a0001c0001t0001g0080a0001c0001t0001g0124a0001c0001t0001g0180others(7): Show | 10 | HG00642.hp1 HG01069.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.4093+985delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740615 | ||||||
chr15:48740807
|
TG | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(70): Show | 75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.4093+793delC | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740807 | ||||||
chr15:48740851
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4093+750A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740851 | ||||||
chr15:48740931
|
A | G | 6 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(3): Show | 6 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.4093+670T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740931 | ||||||
chr15:48740956
|
A | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(76): Show | 81 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.4093+645T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740956 | ||||||
chr15:48740987
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4093+614G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740987 | ||||||
chr15:48741028
|
A | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.4093+573T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741028 | ||||||
chr15:48741088
|
C | T | 5 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.4093+513G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741088 | ||||||
chr15:48741118
|
A | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(78): Show | 83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.4093+483T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741118 | ||||||
chr15:48741130
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0004a0001c0001t0001g0107a0001c0001t0001g0215others(7): Show | 11 | HG00738.hp2 HG01071.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4093+462_4093+470d others(11): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741130 | ||||||
chr15:48741130
|
C | CTTTTTTT others(3): Show |
149 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(146): Show | 157 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.4093+461_4093+470d others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741130 | ||||||
chr15:48741130
|
C | CTTTTTTT others(4): Show |
26 | a0001c0001t0001g0017a0001c0001t0001g0064a0001c0001t0001g0092others(23): Show | 26 | HG00140.hp2 HG01099.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.4093+460_4093+470d others(13): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741130 | ||||||
chr15:48741412
|
T | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4093+189A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741412 | ||||||
chr15:48741567
|
T | C | 1 | a0001c0016t0004g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4093+34A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741567 | ||||||
chr15:48741600
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19070.hp2 | splice_donor_variant&intron_variant | HIGH | c.4093+1G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741600 | ||||||
chr15:48742195
|
T | C | 1 | a0011c0039t0002g0256 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3836-95A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742195 | ||||||
chr15:48742260
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3836-160T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742260 | ||||||
chr15:48742307
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3836-207G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742307 | ||||||
chr15:48742308
|
G | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3836-208C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742308 | ||||||
chr15:48742640
|
T | C | 3 | a0001c0001t0001g0226a0002c0002t0002g0001a0002c0002t0002g0270 | 6 | NA18953.hp1 NA18957.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.3836-540A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742640 | ||||||
chr15:48742709
|
C | T | 2 | a0017c0028t0002g0287a0026c0032t0001g0149 | 2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3836-609G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742709 | ||||||
chr15:48742810
|
A | AT | 8 | a0001c0024t0001g0138a0002c0002t0002g0012a0002c0002t0002g0252others(5): Show | 9 | HG02258.hp1 NA18942.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.3836-711dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742810 | ||||||
chr15:48742824
|
T | G | 55 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(52): Show | 59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3836-724A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742824 | ||||||
chr15:48742842
|
C | G | 2 | a0003c0003t0001g0211a0016c0030t0001g0207 | 2 | NA18962.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3836-742G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742842 | ||||||
chr15:48742987
|
A | C | 2 | a0001c0001t0001g0192a0001c0014t0001g0181 | 2 | NA19010.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3836-887T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742987 | ||||||
chr15:48743051
|
A | G | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3836-951T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743051 | ||||||
chr15:48743094
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3836-994T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743094 | ||||||
chr15:48743548
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3835+692G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743548 | ||||||
chr15:48743563
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3835+677A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743563 | ||||||
chr15:48743769
|
T | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.3835+471A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743769 | ||||||
chr15:48744050
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3835+190A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48744050 | ||||||
chr15:48744148
|
G | A | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3835+92C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48744148 | ||||||
chr15:48744220
|
A | C | 2 | a0017c0028t0002g0287a0026c0032t0001g0149 | 2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3835+20T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48744220 | ||||||
chr15:48744705
|
T | C | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3731+191A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/26 | chr15 | 48744705 | ||||||
chr15:48744764
|
T | C | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3731+132A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/26 | chr15 | 48744764 | ||||||
chr15:48745116
|
G | A | 1 | a0002c0002t0006g0265 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3635-124C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745116 | ||||||
chr15:48745266
|
A | G | 1 | a0003c0003t0002g0297 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3635-274T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745266 | ||||||
chr15:48745319
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3635-327T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745319 | ||||||
chr15:48745434
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3635-442A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745434 | ||||||
chr15:48745452
|
T | TTG | 3 | a0003c0003t0001g0161a0003c0003t0001g0172a0003c0003t0002g0295 | 3 | NA18963.hp2 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3635-462_3635-461d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745452 | ||||||
chr15:48745452
|
TTG | T | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.3635-462_3635-461d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745452 | ||||||
chr15:48745732
|
G | A | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(70): Show | 75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3635-740C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745732 | ||||||
chr15:48745943
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3635-951A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745943 | ||||||
chr15:48745954
|
G | A | 1 | a0001c0001t0003g0238 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3635-962C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745954 | ||||||
chr15:48745984
|
C | T | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3635-992G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745984 | ||||||
chr15:48746033
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0060 | 2 | HG00621.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.3635-1041G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746033 | ||||||
chr15:48746159
|
A | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3635-1167T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746159 | ||||||
chr15:48746273
|
C | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(70): Show | 75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3635-1281G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746273 | ||||||
chr15:48746486
|
A | G | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3635-1494T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746486 | ||||||
chr15:48746501
|
C | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3635-1509G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746501 | ||||||
chr15:48746502
|
A | G | 2 | a0001c0024t0001g0138a0024c0018t0001g0232 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3635-1510T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746502 | ||||||
chr15:48746559
|
G | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3635-1567C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746559 | ||||||
chr15:48746655
|
T | C | 2 | a0001c0024t0001g0138a0024c0018t0001g0232 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3635-1663A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746655 | ||||||
chr15:48746671
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 8 | HG02717.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3635-1679C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746671 | ||||||
chr15:48747029
|
G | C | 1 | a0002c0002t0002g0267 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3634+1414C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747029 | ||||||
chr15:48747275
|
G | C | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1168C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747275 | ||||||
chr15:48747288
|
T | C | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1155A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747288 | ||||||
chr15:48747294
|
C | G | 1 | a0025c0027t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3634+1149G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747294 | ||||||
chr15:48747336
|
T | C | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1107A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747336 | ||||||
chr15:48747344
|
A | G | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1099T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747344 | ||||||
chr15:48747429
|
G | T | 1 | a0004c0004t0001g0147 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3634+1014C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747429 | ||||||
chr15:48747513
|
G | A | 1 | a0007c0006t0001g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3634+930C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747513 | ||||||
chr15:48747572
|
A | G | 1 | a0001c0001t0002g0309 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3634+871T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747572 | ||||||
chr15:48747600
|
T | C | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.3634+843A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747600 | ||||||
chr15:48747685
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3634+758T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747685 | ||||||
chr15:48747879
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3634+564C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747879 | ||||||
chr15:48747908
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3634+535A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747908 | ||||||
chr15:48747934
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3634+509C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747934 | ||||||
chr15:48747976
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3634+467G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747976 | ||||||
chr15:48748082
|
T | A | 1 | a0010c0011t0001g0096 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3634+361A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748082 | ||||||
chr15:48748104
|
T | G | 1 | a0001c0001t0001g0155 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3634+339A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748104 | ||||||
chr15:48748303
|
T | G | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3634+140A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748303 | ||||||
chr15:48748322
|
A | C | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3634+121T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748322 | ||||||
chr15:48748667
|
TA | T | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.3467-58delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48748667 | ||||||
chr15:48749238
|
A | C | 3 | a0001c0001t0002g0246a0001c0001t0002g0247a0001c0001t0002g0298 | 3 | NA18957.hp2 NA18985.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.3467-628T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749238 | ||||||
chr15:48749556
|
A | G | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3467-946T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749556 | ||||||
chr15:48749584
|
A | G | 4 | a0004c0004t0001g0141a0004c0004t0001g0146a0004c0004t0001g0150others(1): Show | 4 | NA18949.hp1 NA19058.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.3467-974T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749584 | ||||||
chr15:48749837
|
GA | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(26): Show | 31 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.3467-1228delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749837 | ||||||
chr15:48750015
|
C | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 48 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.3467-1405G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750015 | ||||||
chr15:48750070
|
A | G | 1 | a0002c0002t0002g0251 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3467-1460T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750070 | ||||||
chr15:48750481
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3466+1868A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750481 | ||||||
chr15:48750647
|
C | T | 5 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.3466+1702G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750647 | ||||||
chr15:48750664
|
T | C | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+1685A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750664 | ||||||
chr15:48750721
|
C | T | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3466+1628G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750721 | ||||||
chr15:48750722
|
A | G | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 138 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.3466+1627T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750722 | ||||||
chr15:48750814
|
A | C | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3466+1535T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750814 | ||||||
chr15:48750820
|
T | C | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3466+1529A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750820 | ||||||
chr15:48750965
|
G | C | 1 | a0004c0004t0001g0145 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3466+1384C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750965 | ||||||
chr15:48751063
|
C | T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+1286G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751063 | ||||||
chr15:48751196
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3466+1153T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751196 | ||||||
chr15:48751351
|
A | G | 1 | a0002c0002t0002g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3466+998T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751351 | ||||||
chr15:48751352
|
G | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+997C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751352 | ||||||
chr15:48751516
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3466+833C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751516 | ||||||
chr15:48751568
|
G | A | 1 | a0012c0013t0001g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3466+781C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751568 | ||||||
chr15:48751652
|
C | A | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 132 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.3466+697G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751652 | ||||||
chr15:48751652
|
C | T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+697G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751652 | ||||||
chr15:48751777
|
C | G | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+572G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751777 | ||||||
chr15:48751792
|
T | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.3466+557A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751792 | ||||||
chr15:48751805
|
C | G | 44 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 47 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.3466+544G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751805 | ||||||
chr15:48752239
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3466+110G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48752239 | ||||||
chr15:48752341
|
C | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
splice_region_variant&intron_variant | LOW | c.3466+8G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48752341 | ||||||
chr15:48752619
|
T | C | 9 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0001g0085others(6): Show | 9 | HG00621.hp2 NA18747.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.3346-150A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752619 | ||||||
chr15:48752730
|
G | C | 1 | a0001c0001t0002g0292 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3346-261C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752730 | ||||||
chr15:48752850
|
G | A | 1 | a0001c0001t0001g0002 | 3 | HG00140.hp1 HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3346-381C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752850 | ||||||
chr15:48752880
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3346-411G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752880 | ||||||
chr15:48753328
|
A | G | 1 | a0004c0004t0001g0146 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3346-859T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753328 | ||||||
chr15:48753483
|
C | G | 1 | a0001c0001t0002g0319 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3346-1014G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753483 | ||||||
chr15:48753567
|
C | T | 43 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 46 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.3346-1098G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753567 | ||||||
chr15:48753670
|
A | G | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3346-1201T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753670 | ||||||
chr15:48754526
|
C | CA | 6 | a0006c0012t0001g0057a0006c0012t0001g0077a0006c0017t0001g0025others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3345+1376dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754526 | ||||||
chr15:48754561
|
G | A | 1 | a0021c0026t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3345+1342C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754561 | ||||||
chr15:48754597
|
G | T | 4 | a0005c0005t0001g0044a0005c0005t0001g0050a0005c0005t0001g0052others(1): Show | 4 | HG02630.hp2 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345+1306C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754597 | ||||||
chr15:48754680
|
T | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+1223A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754680 | ||||||
chr15:48754762
|
C | T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+1141G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754762 | ||||||
chr15:48754852
|
G | A | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3345+1051C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754852 | ||||||
chr15:48754970
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3345+933G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754970 | ||||||
chr15:48755017
|
CT | C | 55 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(52): Show | 59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3345+885delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755017 | ||||||
chr15:48755074
|
C | G | 1 | a0027c0031t0002g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3345+829G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755074 | ||||||
chr15:48755134
|
A | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.3345+769T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755134 | ||||||
chr15:48755134
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0013 | 3 | NA18977.hp1 NA19081.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3345+769T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755134 | ||||||
chr15:48755145
|
C | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0136 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3345+758G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755145 | ||||||
chr15:48755147
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3345+756C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755147 | ||||||
chr15:48755157
|
T | A | 5 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.3345+746A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755157 | ||||||
chr15:48755266
|
G | A | 55 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(52): Show | 59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3345+637C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755266 | ||||||
chr15:48755275
|
G | A | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3345+628C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755275 | ||||||
chr15:48755295
|
A | G | 55 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(52): Show | 59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3345+608T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755295 | ||||||
chr15:48755468
|
T | G | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3345+435A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755468 | ||||||
chr15:48755793
|
A | G | 1 | a0001c0001t0003g0239 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3345+110T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755793 | ||||||
chr15:48755810
|
T | A | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3345+93A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755810 | ||||||
chr15:48756768
|
G | C | 51 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(48): Show | 55 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2695-215C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48756768 | ||||||
chr15:48757007
|
T | C | 1 | a0001c0009t0005g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2695-454A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757007 | ||||||
chr15:48757148
|
C | G | 1 | a0004c0004t0001g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2695-595G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757148 | ||||||
chr15:48757154
|
C | CA | 56 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(53): Show | 60 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.2695-602dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757154 | ||||||
chr15:48757218
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2695-665C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757218 | ||||||
chr15:48757492
|
C | T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2695-939G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757492 | ||||||
chr15:48757603
|
C | T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2695-1050G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757603 | ||||||
chr15:48757626
|
C | T | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.2695-1073G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757626 | ||||||
chr15:48757734
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0063 | 2 | HG00438.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2695-1181T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757734 | ||||||
chr15:48757769
|
G | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2695-1216C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757769 | ||||||
chr15:48757782
|
A | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(138): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2695-1229T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757782 | ||||||
chr15:48757970
|
T | C | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2695-1417A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757970 | ||||||
chr15:48758131
|
T | A | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2695-1578A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758131 | ||||||
chr15:48758252
|
C | T | 1 | a0002c0002t0006g0265 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2695-1699G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758252 | ||||||
chr15:48758279
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2695-1726A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758279 | ||||||
chr15:48758446
|
G | A | 1 | a0001c0001t0002g0314 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2694+1689C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758446 | ||||||
chr15:48758587
|
C | T | 1 | a0029c0015t0001g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2694+1548G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758587 | ||||||
chr15:48758677
|
C | T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2694+1458G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758677 | ||||||
chr15:48758718
|
C | CAA | 25 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0122others(22): Show | 27 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2694+1415_2694+141 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | ||||||
chr15:48758718
|
C | CAAA | 76 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(73): Show | 79 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.2694+1414_2694+141 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | ||||||
chr15:48758718
|
C | CAAAA | 36 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0054others(33): Show | 37 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2694+1413_2694+141 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | ||||||
chr15:48758718
|
C | CAAAAAAA | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 88 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.2694+1410_2694+141 others(11): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | ||||||
chr15:48758718
|
C | CAAAAAAA others(1): Show |
42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(39): Show | 44 | HG00408.hp2 HG01123.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.2694+1409_2694+141 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | ||||||
chr15:48758718
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2694+1405_2694+141 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | ||||||
chr15:48758773
|
T | C | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2694+1362A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758773 | ||||||
chr15:48758901
|
A | G | 1 | a0021c0026t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2694+1234T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758901 | ||||||
chr15:48758976
|
A | G | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2694+1159T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758976 | ||||||
chr15:48759106
|
G | T | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(188): Show | 200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2694+1029C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759106 | ||||||
chr15:48759442
|
T | C | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2694+693A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759442 | ||||||
chr15:48759453
|
C | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 137 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.2694+682G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759453 | ||||||
chr15:48759457
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2694+678A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759457 | ||||||
chr15:48759646
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0136 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2694+489A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759646 | ||||||
chr15:48759715
|
C | G | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2694+420G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759715 | ||||||
chr15:48759752
|
A | G | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2694+383T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759752 | ||||||
chr15:48760336
|
G | C | 1 | a0007c0006t0001g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2563-70C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760336 | ||||||
chr15:48760472
|
A | C | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2563-206T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760472 | ||||||
chr15:48760612
|
A | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(34): Show | 40 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.2563-346T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760612 | ||||||
chr15:48760614
|
T | C | 1 | a0021c0026t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2563-348A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760614 | ||||||
chr15:48760632
|
C | T | 50 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(47): Show | 54 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.2563-366G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760632 | ||||||
chr15:48760704
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2563-438T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760704 | ||||||
chr15:48760999
|
G | C | 7 | a0001c0001t0002g0249a0001c0001t0002g0296a0002c0002t0002g0243others(4): Show | 7 | NA18955.hp1 NA18956.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.2563-733C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760999 | ||||||
chr15:48761053
|
T | G | 51 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(48): Show | 55 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2563-787A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761053 | ||||||
chr15:48761214
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0191a0001c0001t0001g0194others(1): Show | 4 | HG00099.hp1 HG00642.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.2563-948C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761214 | ||||||
chr15:48761243
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2563-977T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761243 | ||||||
chr15:48761381
|
T | C | 3 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0016t0004g0110 | 3 | HG00099.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2562+1010A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761381 | ||||||
chr15:48761649
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2562+742G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761649 | ||||||
chr15:48761786
|
A | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2562+605T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761786 | ||||||
chr15:48762290
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG01496.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2562+101T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48762290 | ||||||
chr15:48762755
|
C | A | 43 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(40): Show | 46 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.2281-83G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762755 | ||||||
chr15:48762909
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2281-237A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762909 | ||||||
chr15:48762965
|
T | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(75): Show | 80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.2281-293A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762965 | ||||||
chr15:48762989
|
T | TA | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 134 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.2281-318dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762989 | ||||||
chr15:48763034
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2281-362A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763034 | ||||||
chr15:48763098
|
G | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2281-426C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763098 | ||||||
chr15:48763138
|
G | A | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 138 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.2281-466C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763138 | ||||||
chr15:48763214
|
C | T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2281-542G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763214 | ||||||
chr15:48763263
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2281-591A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763263 | ||||||
chr15:48763404
|
T | G | 1 | a0004c0004t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2281-732A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763404 | ||||||
chr15:48763509
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2281-837T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763509 | ||||||
chr15:48763640
|
C | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2281-968G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763640 | ||||||
chr15:48763690
|
A | AT | 3 | a0003c0003t0001g0160a0003c0003t0001g0161a0003c0003t0001g0172 | 3 | HG02080.hp2 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2281-1019dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763690 | ||||||
chr15:48763917
|
T | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(27): Show | 32 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.2281-1245A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763917 | ||||||
chr15:48763994
|
T | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2281-1322A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763994 | ||||||
chr15:48764047
|
C | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2281-1375G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764047 | ||||||
chr15:48764092
|
A | G | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2281-1420T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764092 | ||||||
chr15:48764473
|
T | G | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(188): Show | 200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2281-1801A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764473 | ||||||
chr15:48764607
|
G | A | 1 | a0002c0002t0002g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2281-1935C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764607 | ||||||
chr15:48764937
|
C | T | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2280+2123G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764937 | ||||||
chr15:48764942
|
C | G | 1 | a0004c0004t0001g0145 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2280+2118G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764942 | ||||||
chr15:48764992
|
TA | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0148a0002c0002t0002g0250others(3): Show | 6 | HG00597.hp2 HG01257.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2280+2067delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764992 | ||||||
chr15:48765056
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2280+2004G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765056 | ||||||
chr15:48765066
|
A | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2280+1994T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765066 | ||||||
chr15:48765279
|
C | T | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.2280+1781G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765279 | ||||||
chr15:48765424
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2280+1636A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765424 | ||||||
chr15:48765471
|
T | C | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2280+1589A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765471 | ||||||
chr15:48765546
|
A | G | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2280+1514T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765546 | ||||||
chr15:48765636
|
A | AT | 52 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0031others(49): Show | 57 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.2280+1423dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATT | 40 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0045others(37): Show | 41 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.2280+1422_2280+142 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTT | 8 | a0001c0001t0001g0105a0001c0001t0002g0296a0001c0001t0002g0298others(5): Show | 8 | HG02886.hp1 HG03516.hp1 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.2280+1421_2280+142 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTT | 8 | a0001c0001t0001g0021a0001c0001t0001g0056a0001c0001t0001g0092others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.2280+1420_2280+142 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0100a0001c0001t0002g0289a0006c0012t0001g0077 | 3 | HG03041.hp1 HG03486.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2280+1412_2280+142 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0002g0288 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2280+1411_2280+142 others(17): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2280+1407_2280+142 others(21): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTTTTT others(11): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0108 | 4 | HG02717.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280+1406_2280+142 others(22): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2280+1405_2280+142 others(23): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2280+1402_2280+142 others(26): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0001g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2280+1400_2280+142 others(28): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
AT | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(51): Show | 56 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2280+1423delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
ATT | A | 21 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0065others(18): Show | 21 | HG00544.hp2 HG00558.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2280+1422_2280+142 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
ATTT | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0064a0001c0001t0001g0223others(3): Show | 6 | HG02922.hp1 HG03209.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.2280+1421_2280+142 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
ATTTT | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(12): Show | 17 | HG00408.hp2 HG01884.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.2280+1420_2280+142 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
ATTTTTTT others(7): Show |
A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2280+1410_2280+142 others(18): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
ATTTTTTT others(10): Show |
A | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2280+1407_2280+142 others(21): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
ATTTTTTT others(11): Show |
A | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2280+1406_2280+142 others(22): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765636
|
ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2280+1404_2280+142 others(24): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | ||||||
chr15:48765699
|
G | C | 1 | a0002c0002t0002g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2280+1361C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765699 | ||||||
chr15:48765802
|
C | T | 1 | a0002c0002t0002g0281 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2280+1258G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765802 | ||||||
chr15:48765873
|
C | T | 1 | a0001c0001t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2280+1187G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765873 | ||||||
chr15:48765995
|
T | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0054others(36): Show | 40 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.2280+1065A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765995 | ||||||
chr15:48766201
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2280+859G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48766201 | ||||||
chr15:48766639
|
C | T | 5 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2280+421G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48766639 | ||||||
chr15:48766787
|
C | CT | 9 | a0001c0001t0002g0296a0001c0001t0002g0318a0002c0002t0002g0012others(6): Show | 10 | HG03225.hp2 HG03927.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.2280+272dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48766787 | ||||||
chr15:48767029
|
G | T | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2280+31C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48767029 | ||||||
chr15:48767476
|
C | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 45 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.2019-13G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767476 | ||||||
chr15:48767506
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0136 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2019-43G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767506 | ||||||
chr15:48767571
|
T | C | 2 | a0021c0026t0001g0131a0027c0031t0002g0321 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2019-108A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767571 | ||||||
chr15:48767745
|
T | G | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2019-282A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767745 | ||||||
chr15:48767804
|
T | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2019-341A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767804 | ||||||
chr15:48767886
|
G | T | 50 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(47): Show | 54 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.2018+333C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767886 | ||||||
chr15:48767947
|
C | T | 1 | a0001c0016t0004g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2018+272G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767947 | ||||||
chr15:48767969
|
C | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.2018+250G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767969 | ||||||
chr15:48767973
|
T | C | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2018+246A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767973 | ||||||
chr15:48768088
|
C | G | 2 | a0021c0026t0001g0131a0027c0031t0002g0321 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2018+131G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48768088 | ||||||
chr15:48768336
|
C | G | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02615.hp1 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.1909-8G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768336 | ||||||
chr15:48768355
|
C | T | 1 | a0005c0005t0001g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1909-27G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768355 | ||||||
chr15:48768489
|
G | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1909-161C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768489 | ||||||
chr15:48768528
|
T | C | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1909-200A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768528 | ||||||
chr15:48768591
|
T | C | 1 | a0001c0001t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1909-263A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768591 | ||||||
chr15:48768645
|
T | A | 1 | a0001c0001t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1908+311A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768645 | ||||||
chr15:48768733
|
T | C | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1908+223A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768733 | ||||||
chr15:48768790
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1908+166G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768790 | ||||||
chr15:48768929
|
TAA | T | 4 | a0003c0003t0001g0047a0003c0003t0001g0143a0003c0003t0001g0227others(1): Show | 4 | HG02056.hp1 NA18985.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908+25_1908+26del others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768929 | ||||||
chr15:48768933
|
A | T | 1 | a0001c0001t0001g0222 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1908+23T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768933 | ||||||
chr15:48769104
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0065 | 2 | NA18948.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1783-23A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769104 | ||||||
chr15:48769111
|
A | G | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1783-30T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769111 | ||||||
chr15:48769114
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0065 | 2 | NA18948.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1783-33A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769114 | ||||||
chr15:48769171
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1783-90G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769171 | ||||||
chr15:48769199
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1783-118T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769199 | ||||||
chr15:48769249
|
T | C | 1 | a0002c0002t0002g0267 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1783-168A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769249 | ||||||
chr15:48769295
|
T | G | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1783-214A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769295 | ||||||
chr15:48769408
|
A | C | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1783-327T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769408 | ||||||
chr15:48769458
|
G | A | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1783-377C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769458 | ||||||
chr15:48769508
|
A | C | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1783-427T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769508 | ||||||
chr15:48769551
|
G | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1783-470C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769551 | ||||||
chr15:48769696
|
A | G | 57 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(54): Show | 61 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1783-615T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769696 | ||||||
chr15:48769778
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1783-697C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769778 | ||||||
chr15:48769783
|
T | C | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1783-702A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769783 | ||||||
chr15:48770273
|
C | T | 1 | a0003c0003t0001g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1783-1192G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770273 | ||||||
chr15:48770489
|
CA | C | 50 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(47): Show | 54 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1783-1409delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770489 | ||||||
chr15:48770918
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1782+1569A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770918 | ||||||
chr15:48770959
|
A | AAAAG | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1782+1527_1782+152 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770959 | ||||||
chr15:48770987
|
G | A | 1 | a0025c0027t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1782+1500C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770987 | ||||||
chr15:48770993
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1782+1494T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770993 | ||||||
chr15:48771027
|
T | C | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1782+1460A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771027 | ||||||
chr15:48771232
|
T | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(74): Show | 79 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1782+1255A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771232 | ||||||
chr15:48771271
|
CAA | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 131 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1782+1214_1782+121 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771271 | ||||||
chr15:48771336
|
G | C | 1 | a0002c0002t0002g0267 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1782+1151C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771336 | ||||||
chr15:48771344
|
A | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1782+1143T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771344 | ||||||
chr15:48771457
|
G | A | 45 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 48 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.1782+1030C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771457 | ||||||
chr15:48772154
|
G | A | 3 | a0006c0012t0001g0057a0006c0012t0001g0077a0027c0031t0002g0321 | 3 | HG01891.hp1 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1782+333C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772154 | ||||||
chr15:48772175
|
T | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 130 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1782+312A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772175 | ||||||
chr15:48772275
|
G | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1782+212C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772275 | ||||||
chr15:48772325
|
C | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1782+162G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772325 | ||||||
chr15:48772429
|
A | C | 6 | a0001c0001t0001g0173a0001c0001t0001g0217a0001c0001t0001g0220others(3): Show | 6 | HG02015.hp1 NA18942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+58T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772429 | ||||||
chr15:48772697
|
G | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0065 | 3 | NA18948.hp1 NA18961.hp2 NA18984.hp1 |
splice_region_variant&intron_variant | LOW | c.1578-6C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48772697 | ||||||
chr15:48773259
|
A | C | 2 | a0006c0012t0001g0057a0006c0012t0001g0077 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1578-568T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773259 | ||||||
chr15:48773346
|
G | A | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1578-655C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773346 | ||||||
chr15:48773441
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1578-750G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773441 | ||||||
chr15:48773492
|
T | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1578-801A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773492 | ||||||
chr15:48773561
|
G | A | 1 | a0001c0001t0002g0314 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1578-870C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773561 | ||||||
chr15:48773586
|
A | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1578-895T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773586 | ||||||
chr15:48773837
|
A | G | 1 | a0003c0003t0001g0210 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1578-1146T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773837 | ||||||
chr15:48773881
|
T | C | 55 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(52): Show | 59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1578-1190A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773881 | ||||||
chr15:48774005
|
T | C | 1 | a0027c0031t0002g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1578-1314A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774005 | ||||||
chr15:48774080
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG01496.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-1389A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774080 | ||||||
chr15:48774428
|
T | C | 1 | a0007c0006t0001g0026 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1578-1737A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774428 | ||||||
chr15:48774455
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1578-1764C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774455 | ||||||
chr15:48774471
|
G | A | 1 | a0008c0008t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1578-1780C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774471 | ||||||
chr15:48774484
|
C | A | 1 | a0001c0001t0004g0136 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1578-1793G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774484 | ||||||
chr15:48774523
|
C | T | 1 | a0003c0003t0001g0227 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1578-1832G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774523 | ||||||
chr15:48774705
|
C | CTG | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578-2015_1578-201 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774705 | ||||||
chr15:48774793
|
A | T | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578-2102T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774793 | ||||||
chr15:48775140
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1578-2449T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775140 | ||||||
chr15:48775525
|
A | G | 1 | a0027c0031t0002g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1578-2834T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775525 | ||||||
chr15:48775559
|
T | C | 1 | a0002c0002t0002g0268 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1578-2868A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775559 | ||||||
chr15:48775588
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1578-2897A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775588 | ||||||
chr15:48775663
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1578-2972T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775663 | ||||||
chr15:48775664
|
T | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1578-2973A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775664 | ||||||
chr15:48775724
|
T | A | 51 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(48): Show | 55 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1578-3033A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775724 | ||||||
chr15:48775780
|
T | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1578-3089A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775780 | ||||||
chr15:48775922
|
TA | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(322): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1578-3232delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775922 | ||||||
chr15:48775946
|
C | T | 2 | a0001c0001t0001g0038a0002c0002t0002g0280 | 2 | NA18990.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1578-3255G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775946 | ||||||
chr15:48776039
|
G | GAA | 56 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(53): Show | 60 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1578-3350_1578-334 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776039 | ||||||
chr15:48776137
|
C | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0136 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1578-3446G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776137 | ||||||
chr15:48776161
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0136 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1578-3470T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776161 | ||||||
chr15:48776484
|
C | A | 1 | a0002c0002t0002g0271 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1578-3793G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776484 | ||||||
chr15:48776582
|
T | C | 2 | a0001c0001t0001g0188a0008c0008t0001g0189 | 2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1578-3891A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776582 | ||||||
chr15:48776888
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0107 | 2 | HG01169.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1578-4197C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776888 | ||||||
chr15:48776913
|
T | C | 2 | a0002c0002t0002g0254a0002c0002t0002g0268 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1578-4222A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776913 | ||||||
chr15:48776994
|
G | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1577+4202C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776994 | ||||||
chr15:48777138
|
A | C | 1 | a0023c0019t0001g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1577+4058T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777138 | ||||||
chr15:48777198
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1577+3998A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777198 | ||||||
chr15:48777308
|
G | A | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1577+3888C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777308 | ||||||
chr15:48777325
|
G | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 130 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1577+3871C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777325 | ||||||
chr15:48777466
|
T | TTG | 8 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0004g0129others(5): Show | 8 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1577+3728_1577+372 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
T | TTGTG | 12 | a0001c0001t0001g0164a0001c0001t0001g0214a0001c0001t0001g0215others(9): Show | 12 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1577+3726_1577+372 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
T | TTGTGTG | 33 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 36 | HG00408.hp2 HG01109.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.1577+3724_1577+372 others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
T | TTGTGTGT others(1): Show |
38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(35): Show | 40 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1577+3722_1577+372 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
T | TTGTGTGT others(3): Show |
23 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0059others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1577+3720_1577+372 others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
T | TTGTGTGT others(5): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0112a0001c0001t0002g0316others(5): Show | 8 | HG00323.hp1 HG01106.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1577+3718_1577+372 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
T | TTGTGTGT others(7): Show |
3 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0308 | 3 | HG02155.hp1 NA18949.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1577+3716_1577+372 others(18): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
T | TTGTGTGT others(9): Show |
1 | a0002c0002t0002g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1577+3714_1577+372 others(20): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
TTG | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(128): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1577+3728_1577+372 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777466
|
TTGTGTG | T | 4 | a0001c0001t0001g0078a0003c0003t0002g0295a0011c0039t0002g0256others(1): Show | 4 | HG01884.hp1 HG02074.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1577+3724_1577+372 others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | ||||||
chr15:48777515
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1577+3681G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777515 | ||||||
chr15:48777637
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1577+3559T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777637 | ||||||
chr15:48777638
|
T | C | 1 | a0008c0008t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1577+3558A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777638 | ||||||
chr15:48777703
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1577+3493A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777703 | ||||||
chr15:48777848
|
G | A | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1577+3348C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777848 | ||||||
chr15:48777995
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1577+3201A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777995 | ||||||
chr15:48778405
|
C | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1577+2791G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778405 | ||||||
chr15:48778467
|
G | A | 1 | a0001c0001t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1577+2729C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778467 | ||||||
chr15:48778616
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0127a0001c0001t0001g0130others(3): Show | 8 | HG00140.hp1 HG00280.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1577+2580G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778616 | ||||||
chr15:48778672
|
G | A | 5 | a0006c0012t0001g0057a0006c0012t0001g0077a0006c0017t0001g0025others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1577+2524C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778672 | ||||||
chr15:48778674
|
G | T | 1 | a0002c0002t0002g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1577+2522C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778674 | ||||||
chr15:48778677
|
C | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1577+2519G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778677 | ||||||
chr15:48778715
|
C | T | 9 | a0001c0001t0001g0164a0001c0001t0002g0288a0001c0001t0002g0289others(6): Show | 9 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1577+2481G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778715 | ||||||
chr15:48778779
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG02451.hp2 HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1577+2417C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778779 | ||||||
chr15:48778852
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1577+2344C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778852 | ||||||
chr15:48778949
|
C | CA | 17 | a0001c0001t0001g0017a0001c0001t0001g0083a0001c0001t0001g0084others(14): Show | 17 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1577+2246dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778949 | ||||||
chr15:48778965
|
G | C | 17 | a0001c0001t0001g0082a0001c0001t0001g0135a0001c0001t0001g0178others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1577+2231C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778965 | ||||||
chr15:48779010
|
G | A | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1577+2186C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779010 | ||||||
chr15:48779348
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1577+1848T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779348 | ||||||
chr15:48779613
|
C | A | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1577+1583G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779613 | ||||||
chr15:48779639
|
G | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(26): Show | 31 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.1577+1557C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779639 | ||||||
chr15:48779884
|
C | A | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1577+1312G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779884 | ||||||
chr15:48779930
|
G | A | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1577+1266C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779930 | ||||||
chr15:48780277
|
G | A | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1577+919C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780277 | ||||||
chr15:48780483
|
T | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1577+713A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780483 | ||||||
chr15:48780583
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0002g0322 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1577+613A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780583 | ||||||
chr15:48780590
|
T | G | 2 | a0001c0001t0001g0078a0001c0001t0002g0322 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1577+606A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780590 | ||||||
chr15:48780780
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0059a0013c0035t0001g0071 | 3 | NA18943.hp1 NA18962.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1577+416G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780780 | ||||||
chr15:48780830
|
C | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1577+366G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780830 | ||||||
chr15:48780838
|
G | A | 1 | a0004c0004t0001g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1577+358C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780838 | ||||||
chr15:48781052
|
C | G | 1 | a0029c0015t0001g0142 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1577+144G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781052 | ||||||
chr15:48781080
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0136 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1577+116T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781080 | ||||||
chr15:48781099
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0127others(20): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1577+97A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781099 | ||||||
chr15:48781190
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG01496.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1577+6G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781190 | ||||||
chr15:48781706
|
A | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1414-347T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781706 | ||||||
chr15:48781719
|
G | C | 17 | a0001c0001t0001g0082a0001c0001t0001g0135a0001c0001t0001g0178others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1414-360C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781719 | ||||||
chr15:48781726
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1414-367C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781726 | ||||||
chr15:48781799
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0002g0326 | 2 | HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1413+340A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781799 | ||||||
chr15:48781895
|
G | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0148a0002c0002t0002g0250others(2): Show | 5 | HG00597.hp2 HG02129.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1413+244C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781895 | ||||||
chr15:48781938
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1413+201C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781938 | ||||||
chr15:48781996
|
G | A | 1 | a0003c0003t0001g0158 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1413+143C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781996 | ||||||
chr15:48782034
|
G | C | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1413+105C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48782034 | ||||||
chr15:48782342
|
C | T | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 130 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1322-112G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782342 | ||||||
chr15:48782505
|
C | G | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1322-275G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782505 | ||||||
chr15:48782667
|
C | T | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1322-437G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782667 | ||||||
chr15:48782721
|
AT | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0065others(1): Show | 4 | NA18948.hp1 NA18961.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1322-492delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782721 | ||||||
chr15:48782818
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1322-588T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782818 | ||||||
chr15:48782967
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1322-737G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782967 | ||||||
chr15:48783032
|
T | G | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(73): Show | 78 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1322-802A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783032 | ||||||
chr15:48783263
|
G | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1321+710C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783263 | ||||||
chr15:48783479
|
T | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1321+494A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783479 | ||||||
chr15:48783506
|
G | C | 3 | a0007c0006t0001g0018a0007c0006t0001g0019a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1321+467C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783506 | ||||||
chr15:48783621
|
C | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1321+352G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783621 | ||||||
chr15:48783706
|
T | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1321+267A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783706 | ||||||
chr15:48783721
|
T | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0127others(20): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1321+252A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783721 | ||||||
chr15:48783775
|
G | GTA | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(142): Show | 151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1321+196_1321+197d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783775 | ||||||
chr15:48783775
|
G | GTATA | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(34): Show | 39 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.1321+194_1321+197d others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783775 | ||||||
chr15:48783775
|
G | GTATATA | 7 | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0001g0100others(4): Show | 8 | HG02717.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321+192_1321+197d others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783775 | ||||||
chr15:48783791
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0225a0002c0002t0002g0255 | 3 | HG02738.hp1 NA18971.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.1321+182C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783791 | ||||||
chr15:48783892
|
T | G | 1 | a0001c0001t0001g0213 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1321+81A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783892 | ||||||
chr15:48784379
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1174-259T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784379 | ||||||
chr15:48784476
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0002g0326 | 2 | HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1174-356A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784476 | ||||||
chr15:48784482
|
T | C | 5 | a0006c0012t0001g0057a0006c0012t0001g0077a0006c0017t0001g0025others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-362A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784482 | ||||||
chr15:48784529
|
A | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-409T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784529 | ||||||
chr15:48784589
|
C | T | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1174-469G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784589 | ||||||
chr15:48784721
|
C | A | 2 | a0001c0001t0002g0306a0001c0001t0002g0307 | 2 | NA18961.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1174-601G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784721 | ||||||
chr15:48784882
|
T | C | 3 | a0003c0003t0001g0160a0003c0003t0001g0161a0003c0003t0001g0172 | 3 | HG02080.hp2 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1174-762A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784882 | ||||||
chr15:48785231
|
G | C | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1174-1111C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785231 | ||||||
chr15:48785266
|
T | C | 5 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1146A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785266 | ||||||
chr15:48785406
|
T | TCTCAAG | 5 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0001t0004g0129others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1287_1174-128 others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785406 | ||||||
chr15:48785619
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1174-1499A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785619 | ||||||
chr15:48785732
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1174-1612A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785732 | ||||||
chr15:48785864
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1174-1744G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785864 | ||||||
chr15:48785918
|
AAAGAG | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 123 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1174-1803_1174-179 others(9): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785918 | ||||||
chr15:48785919
|
AAGAG | A | 3 | a0001c0001t0001g0226a0002c0002t0002g0001a0002c0002t0002g0270 | 6 | NA18953.hp1 NA18957.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-1803_1174-180 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785919 | ||||||
chr15:48785984
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1174-1864C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785984 | ||||||
chr15:48786026
|
A | C | 3 | a0001c0001t0004g0049a0001c0001t0004g0086a0001c0016t0004g0110 | 3 | HG00099.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1174-1906T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786026 | ||||||
chr15:48786062
|
AGT | A | 48 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0038others(45): Show | 52 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1174-1944_1174-194 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786062 | ||||||
chr15:48786314
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1174-2194T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786314 | ||||||
chr15:48786385
|
C | CA | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1174-2266dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786385 | ||||||
chr15:48786606
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1173+2195G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786606 | ||||||
chr15:48786685
|
A | AAAT | 29 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0092others(26): Show | 30 | HG00735.hp2 HG01981.hp2 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+2113_1173+211 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786685 | ||||||
chr15:48786769
|
G | A | 37 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0123others(34): Show | 37 | HG00140.hp2 HG00621.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1173+2032C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786769 | ||||||
chr15:48786948
|
A | T | 4 | a0002c0002t0002g0012a0002c0002t0002g0272a0002c0002t0002g0276others(1): Show | 5 | NA18952.hp1 NA18964.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+1853T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786948 | ||||||
chr15:48786993
|
C | G | 1 | a0001c0009t0005g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1173+1808G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786993 | ||||||
chr15:48787156
|
A | C | 2 | a0018c0025t0001g0231a0024c0018t0001g0232 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1173+1645T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787156 | ||||||
chr15:48787163
|
G | GTTTTTTG others(1): Show |
14 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG01175.hp2 HG01978.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1173+1637_1173+163 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
G | GTTTTTTG others(3): Show |
2 | a0001c0001t0001g0188a0008c0008t0001g0189 | 2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1173+1637_1173+163 others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
G | GTTTTTTT others(1): Show |
29 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0035others(26): Show | 30 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+1630_1173+163 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
G | GTTTTTTT others(2): Show |
73 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 76 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1173+1629_1173+163 others(13): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
G | GTTTTTTT others(3): Show |
18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(15): Show | 18 | HG00621.hp2 HG01106.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1173+1628_1173+163 others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1173+1627_1173+163 others(15): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
G | GTTTTTTT others(5): Show |
1 | a0007c0006t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1173+1626_1173+163 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
GT | G | 88 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0038others(85): Show | 94 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1173+1637delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787163
|
GTT | G | 71 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0104others(68): Show | 73 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1173+1636_1173+163 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | ||||||
chr15:48787172
|
T | G | 1 | a0001c0001t0002g0308 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1173+1629A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787172 | ||||||
chr15:48787182
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1173+1619A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787182 | ||||||
chr15:48787232
|
A | G | 1 | a0007c0006t0001g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1173+1569T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787232 | ||||||
chr15:48787264
|
C | CTTG | 5 | a0001c0001t0001g0109a0001c0001t0004g0136a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+1536_1173+153 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787264 | ||||||
chr15:48787352
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1173+1449C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787352 | ||||||
chr15:48787386
|
G | A | 1 | a0023c0019t0001g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1173+1415C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787386 | ||||||
chr15:48787400
|
G | A | 1 | a0002c0002t0002g0272 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1173+1401C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787400 | ||||||
chr15:48787461
|
G | A | 1 | a0022c0020t0001g0069 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1173+1340C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787461 | ||||||
chr15:48787729
|
AC | A | 40 | a0002c0002t0002g0001a0002c0002t0002g0012a0002c0002t0002g0243others(37): Show | 44 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1173+1071delG | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787729 | ||||||
chr15:48788014
|
T | C | 326 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1173+787A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788014 | ||||||
chr15:48788084
|
C | T | 8 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0290others(5): Show | 8 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+717G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788084 | ||||||
chr15:48788118
|
T | C | 2 | a0003c0003t0001g0032a0003c0003t0001g0033 | 2 | NA18992.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1173+683A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788118 | ||||||
chr15:48788148
|
A | C | 9 | a0001c0001t0002g0249a0001c0001t0002g0288a0001c0001t0002g0289others(6): Show | 9 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+653T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788148 | ||||||
chr15:48788326
|
CT | C | 104 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0107others(101): Show | 111 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1173+474delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788326 | ||||||
chr15:48788326
|
CTT | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 156 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1173+473_1173+474d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788326 | ||||||
chr15:48788330
|
T | C | 1 | a0002c0002t0002g0273 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1173+471A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788330 | ||||||
chr15:48788351
|
G | T | 326 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1173+450C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788351 | ||||||
chr15:48788373
|
G | A | 2 | a0001c0001t0001g0079a0007c0006t0001g0018 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+428C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788373 | ||||||
chr15:48788423
|
T | G | 2 | a0001c0001t0004g0136a0020c0021t0001g0137 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1173+378A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788423 | ||||||
chr15:48788427
|
G | A | 1 | a0003c0003t0001g0227 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1173+374C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788427 | ||||||
chr15:48788480
|
C | T | 1 | a0001c0001t0002g0286 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1173+321G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788480 | ||||||
chr15:48788701
|
A | G | 1 | a0001c0001t0003g0234 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1173+100T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788701 | ||||||
chr15:48789135
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0003g0235 | 2 | HG02293.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.973-134G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789135 | ||||||
chr15:48789182
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.973-181G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789182 | ||||||
chr15:48789315
|
G | GC | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.973-315dupG | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789315 | ||||||
chr15:48789340
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0004g0136a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.973-339T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789340 | ||||||
chr15:48789342
|
G | A | 1 | a0003c0003t0001g0210 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.973-341C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789342 | ||||||
chr15:48789659
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.973-658A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789659 | ||||||
chr15:48789944
|
C | T | 1 | a0003c0003t0001g0152 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.973-943G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789944 | ||||||
chr15:48790518
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 5 | HG01496.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.972+719T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790518 | ||||||
chr15:48790550
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0004g0136a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+687G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790550 | ||||||
chr15:48790652
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0004g0136a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+585G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790652 | ||||||
chr15:48790733
|
A | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0094 | 3 | HG00323.hp2 HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.972+504T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790733 | ||||||
chr15:48790825
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.972+412G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790825 | ||||||
chr15:48790853
|
C | G | 1 | a0007c0006t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972+384G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790853 | ||||||
chr15:48790854
|
C | A | 1 | a0007c0006t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972+383G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790854 | ||||||
chr15:48790987
|
T | C | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.972+250A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790987 | ||||||
chr15:48791001
|
C | T | 41 | a0002c0002t0002g0001a0002c0002t0002g0012a0002c0002t0002g0243others(38): Show | 45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.972+236G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48791001 | ||||||
chr15:48791380
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
splice_region_variant&intron_variant | LOW | c.833-4G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791380 | ||||||
chr15:48791421
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.833-45C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791421 | ||||||
chr15:48791677
|
C | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.833-301G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791677 | ||||||
chr15:48791830
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.833-454A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791830 | ||||||
chr15:48792061
|
C | G | 5 | a0001c0001t0001g0109a0001c0001t0004g0136a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-685G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792061 | ||||||
chr15:48792477
|
C | T | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.832+844G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792477 | ||||||
chr15:48792690
|
A | G | 3 | a0006c0017t0001g0025a0007c0006t0001g0018a0007c0006t0001g0026 | 3 | HG01884.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.832+631T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792690 | ||||||
chr15:48792783
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+538T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792783 | ||||||
chr15:48792815
|
A | T | 1 | a0002c0002t0002g0252 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.832+506T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792815 | ||||||
chr15:48792820
|
C | CT | 9 | a0001c0001t0001g0132a0001c0001t0001g0205a0002c0002t0002g0248others(6): Show | 9 | HG01069.hp1 HG01081.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+500dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792820 | ||||||
chr15:48793613
|
A | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18984.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.692-152T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48793613 | ||||||
chr15:48793629
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.692-168G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48793629 | ||||||
chr15:48794203
|
A | T | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.692-742T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794203 | ||||||
chr15:48794252
|
A | T | 1 | a0001c0001t0003g0236 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.692-791T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794252 | ||||||
chr15:48794267
|
A | G | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0119others(4): Show | 7 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.692-806T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794267 | ||||||
chr15:48794675
|
T | C | 16 | a0001c0001t0001g0148a0001c0001t0001g0233a0003c0003t0001g0143others(13): Show | 17 | HG00558.hp2 HG00597.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.692-1214A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794675 | ||||||
chr15:48794802
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.691+1208C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794802 | ||||||
chr15:48794999
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.691+1011C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794999 | ||||||
chr15:48795145
|
A | G | 1 | a0001c0001t0002g0320 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.691+865T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795145 | ||||||
chr15:48795419
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.691+591A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795419 | ||||||
chr15:48795440
|
T | C | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.691+570A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795440 | ||||||
chr15:48795596
|
C | T | 41 | a0002c0002t0002g0001a0002c0002t0002g0012a0002c0002t0002g0243others(38): Show | 45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.691+414G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795596 | ||||||
chr15:48795737
|
T | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 87 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.691+273A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795737 | ||||||
chr15:48796001
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0178a0001c0001t0001g0193others(11): Show | 15 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.691+9C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48796001 | ||||||
chr15:48796197
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.541-37G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796197 | ||||||
chr15:48796280
|
T | TTA | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG02895.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.541-122_541-121dup others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796280 | ||||||
chr15:48796287
|
TATAC | T | 42 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.541-131_541-128del others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796287 | ||||||
chr15:48796287
|
TATACACA others(3): Show |
T | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.541-137_541-128del others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796287 | ||||||
chr15:48796287
|
TATACACA others(7): Show |
T | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.541-141_541-128del others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796287 | ||||||
chr15:48796289
|
T | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0173a0001c0001t0001g0200 | 3 | HG01981.hp1 HG02886.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.541-129A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | ||||||
chr15:48796289
|
T | TAC | 18 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0020others(15): Show | 21 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.541-131_541-130dup others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | ||||||
chr15:48796289
|
TAC | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.541-131_541-130del others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | ||||||
chr15:48796289
|
TACAC | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 167 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.541-133_541-130del others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | ||||||
chr15:48796289
|
TACACAC | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0082a0002c0002t0002g0250others(1): Show | 4 | HG01123.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-135_541-130del others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | ||||||
chr15:48796291
|
C | T | 4 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-131G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796291 | ||||||
chr15:48796295
|
C | T | 37 | a0001c0001t0003g0235a0002c0002t0002g0001a0002c0002t0002g0012others(34): Show | 41 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.541-135G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796295 | ||||||
chr15:48796297
|
C | T | 2 | a0002c0002t0002g0250a0002c0002t0002g0276 | 2 | HG04204.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.541-137G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796297 | ||||||
chr15:48796316
|
A | C | 1 | a0001c0001t0002g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.541-156T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796316 | ||||||
chr15:48796325
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0002g0319 | 2 | HG03669.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.541-165A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796325 | ||||||
chr15:48796356
|
G | A | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.541-196C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796356 | ||||||
chr15:48796399
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.541-239A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796399 | ||||||
chr15:48796487
|
T | A | 1 | a0001c0001t0002g0314 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.541-327A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796487 | ||||||
chr15:48796843
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.540+458T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796843 | ||||||
chr15:48796851
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.540+450A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796851 | ||||||
chr15:48797220
|
T | C | 1 | a0002c0002t0002g0275 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.540+81A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48797220 | ||||||
chr15:48797227
|
C | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.540+74G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48797227 | ||||||
chr15:48797248
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.540+53G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48797248 | ||||||
chr15:48797910
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.191+38T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/26 | chr15 | 48797910 | ||||||
chr15:48797927
|
A | C | 1 | a0001c0001t0002g0320 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.191+21T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/26 | chr15 | 48797927 | ||||||
chr15:48797937
|
C | T | 16 | a0001c0001t0001g0148a0001c0001t0001g0233a0003c0003t0001g0143others(13): Show | 17 | HG00558.hp2 HG00597.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.191+11G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/26 | chr15 | 48797937 | ||||||
chr15:48798157
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.88-106G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798157 | ||||||
chr15:48798261
|
CT | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0098others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.88-211delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798261 | ||||||
chr15:48798430
|
T | C | 1 | a0004c0004t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.88-379A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798430 | ||||||
chr15:48798540
|
CT | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.88-490delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798540 | ||||||
chr15:48798846
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0004g0136a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-795G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798846 | ||||||
chr15:48798916
|
TATA | T | 40 | a0001c0001t0001g0009a0001c0001t0001g0098a0001c0001t0001g0174others(37): Show | 41 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.88-868_88-866delTA others(1): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798916 | ||||||
chr15:48799106
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.88-1055A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799106 | ||||||
chr15:48799160
|
G | GA | 33 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 36 | HG00408.hp2 HG01109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.88-1110dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799160 | ||||||
chr15:48799307
|
T | C | 2 | a0001c0009t0005g0022a0001c0009t0005g0023 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88-1256A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799307 | ||||||
chr15:48799484
|
A | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.88-1433T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799484 | ||||||
chr15:48799617
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.88-1566A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799617 | ||||||
chr15:48799982
|
A | G | 1 | a0001c0001t0003g0234 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.88-1931T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799982 | ||||||
chr15:48800052
|
C | A | 1 | a0001c0001t0001g0092 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.88-2001G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800052 | ||||||
chr15:48800119
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0004g0136a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-2068G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800119 | ||||||
chr15:48800156
|
G | A | 4 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG02698.hp2 HG03831.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-2105C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800156 | ||||||
chr15:48800224
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.88-2173A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800224 | ||||||
chr15:48800646
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.88-2595G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800646 | ||||||
chr15:48801104
|
T | C | 2 | a0018c0025t0001g0231a0024c0018t0001g0232 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.88-3053A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801104 | ||||||
chr15:48801403
|
G | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88-3352C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801403 | ||||||
chr15:48801440
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0016t0004g0110others(1): Show | 4 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-3389T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801440 | ||||||
chr15:48801627
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.88-3576A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801627 | ||||||
chr15:48801738
|
G | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.88-3687C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801738 | ||||||
chr15:48801808
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.87+3755G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801808 | ||||||
chr15:48801952
|
C | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG01175.hp2 HG01978.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.87+3611G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801952 | ||||||
chr15:48802022
|
G | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(36): Show | 41 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.87+3541C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802022 | ||||||
chr15:48802032
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.87+3531C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802032 | ||||||
chr15:48802052
|
T | C | 1 | a0006c0012t0001g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.87+3511A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802052 | ||||||
chr15:48802066
|
G | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(36): Show | 41 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.87+3497C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802066 | ||||||
chr15:48802197
|
G | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.87+3366C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802197 | ||||||
chr15:48802358
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.87+3205T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802358 | ||||||
chr15:48802367
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.87+3196C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802367 | ||||||
chr15:48802437
|
C | A | 1 | a0001c0001t0002g0326 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.87+3126G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802437 | ||||||
chr15:48802446
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87+3117G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802446 | ||||||
chr15:48802637
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.87+2926A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802637 | ||||||
chr15:48802670
|
G | A | 42 | a0002c0002t0002g0001a0002c0002t0002g0012a0002c0002t0002g0243others(39): Show | 46 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.87+2893C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802670 | ||||||
chr15:48802754
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.87+2809G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802754 | ||||||
chr15:48802821
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.87+2742A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802821 | ||||||
chr15:48803005
|
T | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0178a0001c0001t0001g0193others(12): Show | 16 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.87+2558A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803005 | ||||||
chr15:48803170
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.87+2393G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803170 | ||||||
chr15:48803670
|
T | C | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+1893A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803670 | ||||||
chr15:48803819
|
A | G | 2 | a0006c0017t0001g0025a0007c0006t0001g0026 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.87+1744T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803819 | ||||||
chr15:48804103
|
T | C | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.87+1460A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804103 | ||||||
chr15:48804181
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+1382A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804181 | ||||||
chr15:48804377
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.87+1186C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804377 | ||||||
chr15:48804452
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.87+1111A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804452 | ||||||
chr15:48804463
|
A | G | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.87+1100T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804463 | ||||||
chr15:48804489
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.87+1074C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804489 | ||||||
chr15:48804608
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.87+955G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804608 | ||||||
chr15:48804818
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.87+745T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804818 | ||||||
chr15:48804859
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.87+704T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804859 | ||||||
chr15:48804878
|
C | A | 41 | a0002c0002t0002g0001a0002c0002t0002g0012a0002c0002t0002g0243others(38): Show | 45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.87+685G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804878 | ||||||
chr15:48805037
|
A | G | 1 | a0001c0024t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.87+526T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805037 | ||||||
chr15:48805438
|
G | GT | 42 | a0001c0001t0002g0249a0002c0002t0002g0001a0002c0002t0002g0012others(39): Show | 46 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.87+124dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805438 | ||||||
chr15:48805439
|
T | G | 1 | a0020c0021t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.87+124A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805439 | ||||||
chr15:48805448
|
T | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 34 | HG00408.hp2 HG01109.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.87+115A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805448 | ||||||
chr15:48805449
|
A | T | 4 | a0001c0001t0001g0031a0003c0003t0001g0030a0003c0003t0001g0032others(1): Show | 4 | HG02027.hp1 HG02040.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+114T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805449 | ||||||
chr15:48805535
|
C | CT | 116 | a0001c0001t0001g0013a0001c0001t0001g0104a0001c0001t0001g0105others(113): Show | 122 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.87+27dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805535 | ||||||
chr15:48805536
|
T | TC | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 98 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.87+26_87+27insG | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805536 | ||||||
chr15:48805537
|
T | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 34 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.87+26A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805537 | ||||||
chr15:48805538
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.87+25A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805538 | ||||||
chr15:48805819
|
C | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-7-163G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48805819 | ||||||
chr15:48805825
|
T | C | 5 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(2): Show | 5 | HG00140.hp2 HG01099.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-169A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48805825 | ||||||
chr15:48806483
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7-827G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806483 | ||||||
chr15:48806506
|
T | A | 1 | a0024c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-7-850A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806506 | ||||||
chr15:48806558
|
G | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(36): Show | 41 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-7-902C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806558 | ||||||
chr15:48806690
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-7-1034G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806690 | ||||||
chr15:48806964
|
G | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0212others(18): Show | 23 | HG00408.hp2 HG01109.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.-7-1308C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806964 | ||||||
chr15:48806992
|
T | C | 1 | a0018c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-1336A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806992 | ||||||
chr15:48807561
|
C | CA | 18 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(15): Show | 18 | HG00323.hp2 HG00642.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7-1906dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807561 | ||||||
chr15:48807561
|
CA | C | 149 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.-7-1906delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807561 | ||||||
chr15:48807561
|
CAA | C | 42 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(39): Show | 42 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-7-1907_-7-1906del others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807561 | ||||||
chr15:48807718
|
C | T | 41 | a0001c0001t0002g0249a0002c0002t0002g0001a0002c0002t0002g0012others(38): Show | 45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-7-2062G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807718 | ||||||
chr15:48807782
|
T | C | 40 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0140others(37): Show | 42 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-7-2126A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807782 | ||||||
chr15:48807904
|
T | TTAAAG | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-7-2253_-7-2249dup others(5): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807904 | ||||||
chr15:48807932
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-7-2276T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807932 | ||||||
chr15:48808083
|
C | A | 1 | a0003c0003t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-7-2427G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808083 | ||||||
chr15:48808513
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG01175.hp2 HG01978.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-8+2448G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808513 | ||||||
chr15:48808546
|
A | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0212others(20): Show | 25 | HG00408.hp2 HG01109.hp1 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+2415T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808546 | ||||||
chr15:48808785
|
G | T | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | NA18957.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-8+2176C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808785 | ||||||
chr15:48808956
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+2005T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808956 | ||||||
chr15:48808983
|
C | T | 2 | a0001c0001t0001g0233a0024c0018t0001g0232 | 2 | HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+1978G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808983 | ||||||
chr15:48809005
|
T | C | 2 | a0001c0001t0001g0233a0024c0018t0001g0232 | 2 | HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+1956A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809005 | ||||||
chr15:48809008
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-8+1953G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809008 | ||||||
chr15:48809077
|
A | T | 1 | a0001c0001t0001g0174 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-8+1884T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809077 | ||||||
chr15:48809272
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-8+1689A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809272 | ||||||
chr15:48809294
|
T | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-8+1667A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809294 | ||||||
chr15:48809312
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8+1649G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809312 | ||||||
chr15:48809610
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-8+1351A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809610 | ||||||
chr15:48809634
|
G | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0098a0001c0001t0001g0174others(37): Show | 41 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.-8+1327C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809634 | ||||||
chr15:48809693
|
G | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0016t0004g0110others(2): Show | 5 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+1268C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809693 | ||||||
chr15:48809799
|
A | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0001g0100others(8): Show | 12 | HG01169.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+1162T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809799 | ||||||
chr15:48809840
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-8+1121C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809840 | ||||||
chr15:48809938
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8+1023T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809938 | ||||||
chr15:48810130
|
A | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-8+831T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810130 | ||||||
chr15:48810183
|
T | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0212others(18): Show | 23 | HG00408.hp2 HG01109.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8+778A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810183 | ||||||
chr15:48810190
|
T | C | 3 | a0001c0001t0001g0233a0018c0025t0001g0231a0024c0018t0001g0232 | 3 | HG01884.hp1 HG02451.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+771A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810190 | ||||||
chr15:48810468
|
G | T | 2 | a0010c0011t0001g0096a0010c0011t0001g0097 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-8+493C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810468 | ||||||
chr15:48810622
|
T | C | 3 | a0001c0001t0001g0233a0018c0025t0001g0231a0024c0018t0001g0232 | 3 | HG01884.hp1 HG02451.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+339A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810622 | ||||||
chr15:48810688
|
C | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-8+273G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810688 | ||||||
chr15:48810703
|
A | C | 1 | a0001c0001t0001g0013 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-8+258T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810703 |