geneid | 85459 |
---|---|
ensemblid | ENSG00000166004.15 |
hgncid | 29366 |
symbol | CEP295 |
name | centrosomal protein 295 |
refseq_nuc | NM_033395.2 |
refseq_prot | NP_203753.1 |
ensembl_nuc | ENST00000325212.11 |
ensembl_prot | ENSP00000316681.6 |
mane_status | MANE Select |
chr | chr11 |
start | 93661682 |
end | 93730358 |
strand | + |
ver | v1.2 |
region | chr11:93661682-93730358 |
region5000 | chr11:93656682-93735358 |
regionname0 | CEP295_chr11_93661682_93730358 |
regionname5000 | CEP295_chr11_93656682_93735358 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2601 | 194 | 23 | 33 | 100 | 11 | 26 | 82 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0002 | 0/0 | 2601 | 39 | 0 | 2 | 36 | 0 | 1 | 26 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0003 | 1/0 | 2601 | 39 | 27 | 6 | 4 | 0 | 1 | 4 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004 | 0/0 | 2601 | 17 | 7 | 6 | 0 | 3 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005 | 0/0 | 2601 | 15 | 12 | 2 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0006 | 0/0 | 2601 | 13 | 0 | 0 | 13 | 0 | 0 | 12 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0007 | 0/0 | 2601 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0008 | 0/0 | 2601 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0009 | 0/0 | 2601 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0010 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0011 | 0/0 | 2601 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0012 | 0/0 | 2601 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0013 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0014 | 0/0 | 192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0015 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0016 | 0/0 | 2601 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0017 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0018 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0019 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0020 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0021 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0022 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0023 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0024 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0025 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0026 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0027 | 0/0 | 2601 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0028 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0029 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0030 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0031 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0032 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0033 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 7806 | 187 | 23 | 33 | 98 | 9 | 24 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0002 | 0/0 | 7806 | 39 | 0 | 2 | 36 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0003 | 1/0 | 7806 | 34 | 22 | 6 | 4 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0004 | 0/0 | 7806 | 12 | 0 | 0 | 12 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0005 | 0/0 | 7806 | 12 | 2 | 6 | 0 | 3 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0006 | 0/0 | 7806 | 9 | 8 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0007 | 0/0 | 7806 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0008 | 0/0 | 7806 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0009 | 0/0 | 7806 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0010 | 0/0 | 7806 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0011 | 0/0 | 7806 | 2 | 1 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0012 | 0/1 | 7806 | 2 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0013 | 0/0 | 7806 | 2 | 0 | 0 | 0 | 0 | 2 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0014 | 0/0 | 7806 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0015 | 0/0 | 7806 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0016 | 0/0 | 7806 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0017 | 0/0 | 7806 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0018 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0019 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0020 | 0/0 | 7806 | 2 | 0 | 0 | 1 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0021 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0022 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0023 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0024 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0025 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0026 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0027 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0028 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0029 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0030 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0031 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0032 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0033 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0034 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0035 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0036 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0037 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0038 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0039 | 0/0 | 7850 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0040 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0041 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0042 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0043 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0044 | 0/0 | 7784 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0045 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0046 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
c0047 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 209 | 350 | 83 | 51 | 168 | 14 | 32 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
t0002 | 0/0 | 209 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
t0003 | 0/0 | 209 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
t0004 | 0/0 | 209 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 7806 | 187 | 23 | 33 | 98 | 9 | 24 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0012 | 0/1 | 7806 | 2 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0013 | 0/0 | 7806 | 2 | 0 | 0 | 0 | 0 | 2 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0016 | 0/0 | 7806 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0032 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0002c0002 | 0/0 | 7806 | 39 | 0 | 2 | 36 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0003c0003 | 1/0 | 7806 | 34 | 22 | 6 | 4 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0003c0010 | 0/0 | 7806 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0003c0019 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0005 | 0/0 | 7806 | 12 | 2 | 6 | 0 | 3 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0009 | 0/0 | 7806 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0043 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0047 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0006 | 0/0 | 7806 | 9 | 8 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0011 | 0/0 | 7806 | 2 | 1 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0014 | 0/0 | 7806 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0026 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0033 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0006c0004 | 0/0 | 7806 | 12 | 0 | 0 | 12 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0006c0037 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0007c0007 | 0/0 | 7806 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0008c0008 | 0/0 | 7806 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0009c0017 | 0/0 | 7806 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0010c0018 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0011c0020 | 0/0 | 7806 | 2 | 0 | 0 | 1 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0012c0015 | 0/0 | 7806 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0013c0021 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0014c0044 | 0/0 | 7784 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0015c0035 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0016c0034 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0017c0036 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0018c0024 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0019c0045 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0020c0025 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0021c0046 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0022c0030 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0023c0031 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0024c0028 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0025c0029 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0026c0027 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0027c0023 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0028c0022 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0029c0039 | 0/0 | 7850 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0030c0040 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0031c0038 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0032c0041 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0033c0042 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8014 | 187 | 23 | 33 | 98 | 9 | 24 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0012t0001 | 0/1 | 8014 | 2 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0013t0001 | 0/0 | 8014 | 2 | 0 | 0 | 0 | 0 | 2 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0016t0001 | 0/0 | 8014 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0001c0032t0001 | 0/0 | 8014 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0002c0002t0001 | 0/0 | 8014 | 39 | 0 | 2 | 36 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0003c0003t0001 | 1/0 | 8014 | 34 | 22 | 6 | 4 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0003c0010t0001 | 0/0 | 8014 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0003c0019t0001 | 0/0 | 8014 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0005t0001 | 0/0 | 8014 | 11 | 1 | 6 | 0 | 3 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0005t0003 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0009t0001 | 0/0 | 8014 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0043t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0004c0047t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0006t0001 | 0/0 | 8014 | 9 | 8 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0011t0001 | 0/0 | 8014 | 2 | 1 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0014t0001 | 0/0 | 8014 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0026t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0005c0033t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0006c0004t0001 | 0/0 | 8014 | 12 | 0 | 0 | 12 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0006c0037t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0007c0007t0001 | 0/0 | 8014 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0008c0008t0001 | 0/0 | 8014 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0009c0017t0002 | 0/0 | 8014 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0010c0018t0001 | 0/0 | 8014 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0011c0020t0001 | 0/0 | 8014 | 2 | 0 | 0 | 1 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0012c0015t0001 | 0/0 | 8014 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0013c0021t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0014c0044t0001 | 0/0 | 7992 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0015c0035t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0016c0034t0001 | 0/0 | 8014 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0017c0036t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0018c0024t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0019c0045t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0020c0025t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0021c0046t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0022c0030t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0023c0031t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0024c0028t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0025c0029t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0026c0027t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0027c0023t0001 | 0/0 | 8014 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0028c0022t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0029c0039t0001 | 0/0 | 8058 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0030c0040t0004 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0031c0038t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0032c0041t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
a0033c0042t0001 | 0/0 | 8014 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | copy fasta | chr11 | 93656682 | 93735358 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0012t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0012t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0013t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0013t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0016t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0032t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0010t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0010t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0019t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0019t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0009t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0009t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0009t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0043t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0047t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0011t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0011t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0014t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0014t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0026t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0033t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0037t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0008c0008t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0008c0008t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0008c0008t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0008c0008t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0009c0017t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0009c0017t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0010c0018t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0010c0018t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0011c0020t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0011c0020t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0012c0015t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0012c0015t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0013c0021t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0014c0044t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0015c0035t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0016c0034t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0017c0036t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0018c0024t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0019c0045t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0020c0025t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0021c0046t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0022c0030t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0023c0031t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0024c0028t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0025c0029t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0026c0027t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0027c0023t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0028c0022t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0029c0039t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0030c0040t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0031c0038t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0032c0041t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0033c0042t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0005 | t0001 | g0103 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00140 | hp1 | a0004 | c0005 | t0001 | g0101 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00741 | hp2 | a0005 | c0006 | t0001 | g0044 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01074 | hp2 | a0003 | c0003 | t0001 | g0298 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0291 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01099 | hp1 | a0009 | c0017 | t0002 | g0313 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01106 | hp2 | a0004 | c0005 | t0001 | g0104 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01109 | hp1 | a0016 | c0034 | t0001 | g0060 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01168 | hp1 | a0004 | c0005 | t0001 | g0091 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01169 | hp1 | a0004 | c0005 | t0001 | g0100 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0284 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01243 | hp1 | a0003 | c0003 | t0001 | g0280 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0304 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01255 | hp1 | a0027 | c0023 | t0001 | g0247 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01255 | hp2 | a0004 | c0005 | t0001 | g0114 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01261 | hp2 | a0004 | c0005 | t0001 | g0251 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01361 | hp1 | a0004 | c0005 | t0001 | g0116 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01361 | hp2 | a0003 | c0003 | t0001 | g0282 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01515 | hp1 | a0001 | c0032 | t0001 | g0254 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01884 | hp2 | a0003 | c0010 | t0001 | g0022 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01891 | hp1 | a0003 | c0003 | t0001 | g0293 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01891 | hp2 | a0005 | c0011 | t0001 | g0246 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02004 | hp1 | a0005 | c0014 | t0001 | g0077 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02055 | hp1 | a0004 | c0043 | t0001 | g0125 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02055 | hp2 | a0005 | c0006 | t0001 | g0062 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02056 | hp1 | a0018 | c0024 | t0001 | g0172 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02145 | hp2 | a0007 | c0007 | t0001 | g0073 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02165 | hp1 | a0006 | c0004 | t0001 | g0002 | EAS | CDX | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CDX | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02257 | hp1 | a0005 | c0006 | t0001 | g0040 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0303 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0296 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02280 | hp2 | a0005 | c0014 | t0001 | g0078 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02451 | hp1 | a0008 | c0008 | t0001 | g0083 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02572 | hp1 | a0005 | c0006 | t0001 | g0042 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02572 | hp2 | a0003 | c0010 | t0001 | g0292 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02615 | hp1 | a0003 | c0003 | t0001 | g0281 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02615 | hp2 | a0004 | c0047 | t0001 | g0253 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0285 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0295 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0299 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02683 | hp1 | a0011 | c0020 | t0001 | g0102 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02698 | hp1 | a0003 | c0003 | t0001 | g0286 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02723 | hp1 | a0032 | c0041 | t0001 | g0290 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0302 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02809 | hp1 | a0010 | c0018 | t0001 | g0312 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02818 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02818 | hp2 | a0031 | c0038 | t0001 | g0279 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02886 | hp1 | a0005 | c0006 | t0001 | g0036 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02886 | hp2 | a0010 | c0018 | t0001 | g0311 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02895 | hp2 | a0005 | c0006 | t0001 | g0274 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02897 | hp2 | a0005 | c0006 | t0001 | g0275 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0301 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02965 | hp2 | a0008 | c0008 | t0001 | g0122 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02976 | hp1 | a0004 | c0005 | t0001 | g0086 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0020 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03041 | hp2 | a0005 | c0033 | t0001 | g0039 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0294 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03098 | hp2 | a0005 | c0026 | t0001 | g0045 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03130 | hp1 | a0008 | c0008 | t0001 | g0084 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03130 | hp2 | a0004 | c0009 | t0001 | g0124 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0021 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03139 | hp2 | a0015 | c0035 | t0001 | g0061 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03195 | hp2 | a0003 | c0010 | t0001 | g0022 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03209 | hp1 | a0013 | c0021 | t0001 | g0074 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03209 | hp2 | a0003 | c0003 | t0001 | g0020 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03453 | hp2 | a0003 | c0003 | t0001 | g0283 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03486 | hp1 | a0007 | c0007 | t0001 | g0072 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03540 | hp1 | a0007 | c0007 | t0001 | g0076 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03540 | hp2 | a0004 | c0005 | t0003 | g0026 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03579 | hp1 | a0009 | c0017 | t0002 | g0310 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03579 | hp2 | a0030 | c0040 | t0004 | g0300 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03688 | hp1 | a0004 | c0005 | t0001 | g0008 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03834 | hp2 | a0001 | c0013 | t0001 | g0206 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03942 | hp1 | a0001 | c0013 | t0001 | g0209 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18522 | hp1 | a0005 | c0006 | t0001 | g0043 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18522 | hp2 | a0004 | c0009 | t0001 | g0038 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18940 | hp2 | a0006 | c0004 | t0001 | g0034 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18941 | hp1 | a0006 | c0004 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18949 | hp2 | a0020 | c0025 | t0001 | g0010 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18956 | hp2 | a0028 | c0022 | t0001 | g0250 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18969 | hp1 | a0006 | c0004 | t0001 | g0027 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18971 | hp2 | a0006 | c0004 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18975 | hp2 | a0017 | c0036 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18980 | hp1 | a0019 | c0045 | t0001 | g0008 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18982 | hp1 | a0006 | c0004 | t0001 | g0032 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18985 | hp1 | a0022 | c0030 | t0001 | g0215 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18986 | hp2 | a0029 | c0039 | t0001 | g0307 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18997 | hp2 | a0006 | c0004 | t0001 | g0029 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0308 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19009 | hp2 | a0006 | c0004 | t0001 | g0031 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0287 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19030 | hp2 | a0003 | c0019 | t0001 | g0289 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0305 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19054 | hp1 | a0026 | c0027 | t0001 | g0131 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0309 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19055 | hp1 | a0025 | c0029 | t0001 | g0145 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19058 | hp2 | a0012 | c0015 | t0001 | g0015 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19060 | hp1 | a0023 | c0031 | t0001 | g0228 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19060 | hp2 | a0006 | c0037 | t0001 | g0028 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19062 | hp2 | a0006 | c0004 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19068 | hp2 | a0006 | c0004 | t0001 | g0035 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19074 | hp1 | a0011 | c0020 | t0001 | g0087 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19076 | hp1 | a0014 | c0044 | t0001 | g0081 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19077 | hp1 | a0012 | c0015 | t0001 | g0202 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19077 | hp2 | a0001 | c0016 | t0001 | g0009 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19079 | hp1 | a0006 | c0004 | t0001 | g0033 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19080 | hp2 | a0001 | c0016 | t0001 | g0009 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19086 | hp1 | a0006 | c0004 | t0001 | g0030 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19089 | hp1 | a0021 | c0046 | t0001 | g0117 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19240 | hp2 | a0007 | c0007 | t0001 | g0075 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20752 | hp1 | a0004 | c0005 | t0001 | g0099 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20805 | hp2 | a0001 | c0012 | t0001 | g0184 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20905 | hp1 | a0005 | c0011 | t0001 | g0248 | SAS | GIH | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20905 | hp2 | a0033 | c0042 | t0001 | g0154 | SAS | GIH | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02109 | hp2 | a0024 | c0028 | t0001 | g0041 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02486 | hp2 | a0003 | c0003 | t0001 | g0021 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03471 | hp1 | a0008 | c0008 | t0001 | g0085 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03471 | hp2 | a0003 | c0003 | t0001 | g0297 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20300 | hp1 | a0004 | c0009 | t0001 | g0037 | AFR | USA | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20300 | hp2 | a0005 | c0006 | t0001 | g0276 | AFR | USA | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA21309 | hp1 | a0003 | c0019 | t0001 | g0288 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
homoSapiens_chm13v2 | hp1 | a0001 | c0012 | t0001 | g0222 | REF | REF | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0306 | REF | REF | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93667707
|
A | G | 1 | a0033 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.209A>G | p.Glu70Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/30 | 328/8014 | 209/7806 | 70/2601 | chr11 | 93667707 | ||
chr11:93667736
|
C | A | 2 | a0007a0013 | 5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.238C>A | p.Gln80Lys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/30 | 357/8014 | 238/7806 | 80/2601 | chr11 | 93667736 | ||
chr11:93668910
|
A | G | 1 | a0032 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.412A>G | p.Ile138Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/30 | 531/8014 | 412/7806 | 138/2601 | chr11 | 93668910 | ||
chr11:93675578
|
AAGTAAAA others(15): Show |
A | 1 | a0014 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.538_559delGTAAAAAG others(14): Show |
p.Val180fs | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/30 | 657/8014 | 538/7806 | 180/2601 | INFO_REALIGN_3_PRIME | chr11 | 93675578 | |
chr11:93675665
|
G | A | 28 | a0001a0002a0004others(25): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
missense_variant&splice_region_variant | MODERATE | c.623G>A | p.Arg208Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/30 | 742/8014 | 623/7806 | 208/2601 | chr11 | 93675665 | ||
chr11:93679421
|
C | T | 2 | a0015a0016 | 2 | HG01109.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.634C>T | p.Arg212Cys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/30 | 753/8014 | 634/7806 | 212/2601 | chr11 | 93679421 | ||
chr11:93684086
|
C | A | 1 | a0009 | 2 | HG01099.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.1072C>A | p.Leu358Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/30 | 1191/8014 | 1072/7806 | 358/2601 | chr11 | 93684086 | ||
chr11:93687848
|
C | T | 2 | a0009a0010 | 4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.1319C>T | p.Ser440Phe | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/30 | 1438/8014 | 1319/7806 | 440/2601 | chr11 | 93687848 | ||
chr11:93691763
|
G | A | 1 | a0031 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1417G>A | p.Gly473Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 11/30 | 1536/8014 | 1417/7806 | 473/2601 | chr11 | 93691763 | ||
chr11:93691993
|
C | A | 28 | a0001a0002a0004others(25): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
missense_variant | MODERATE | c.1496C>A | p.Ala499Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/30 | 1615/8014 | 1496/7806 | 499/2601 | chr11 | 93691993 | ||
chr11:93695549
|
T | C | 1 | a0028 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.1586T>C | p.Ile529Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/30 | 1705/8014 | 1586/7806 | 529/2601 | chr11 | 93695549 | ||
chr11:93696716
|
C | G | 1 | a0011 | 2 | HG02683.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.1804C>G | p.Gln602Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 1923/8014 | 1804/7806 | 602/2601 | chr11 | 93696716 | ||
chr11:93696992
|
C | A | 1 | a0027 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.2080C>A | p.Arg694Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2199/8014 | 2080/7806 | 694/2601 | chr11 | 93696992 | ||
chr11:93697356
|
G | C | 1 | a0013 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2444G>C | p.Ser815Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2563/8014 | 2444/7806 | 815/2601 | chr11 | 93697356 | ||
chr11:93697460
|
C | T | 1 | a0008 | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.2548C>T | p.Leu850Phe | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2667/8014 | 2548/7806 | 850/2601 | chr11 | 93697460 | ||
chr11:93697503
|
C | G | 4 | a0006a0009a0010others(1): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.2591C>G | p.Thr864Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2710/8014 | 2591/7806 | 864/2601 | chr11 | 93697503 | ||
chr11:93697575
|
T | C | 2 | a0009a0010 | 4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.2663T>C | p.Phe888Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2782/8014 | 2663/7806 | 888/2601 | chr11 | 93697575 | ||
chr11:93697988
|
G | A | 4 | a0006a0009a0010others(1): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.3076G>A | p.Glu1026Lys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3195/8014 | 3076/7806 | 1026/2601 | chr11 | 93697988 | ||
chr11:93698001
|
T | C | 1 | a0018 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.3089T>C | p.Val1030Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3208/8014 | 3089/7806 | 1030/2601 | chr11 | 93698001 | ||
chr11:93698471
|
G | A | 1 | a0033 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3559G>A | p.Val1187Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3678/8014 | 3559/7806 | 1187/2601 | chr11 | 93698471 | ||
chr11:93698721
|
C | G | 2 | a0006a0017 | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.3809C>G | p.Ala1270Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3928/8014 | 3809/7806 | 1270/2601 | chr11 | 93698721 | ||
chr11:93698765
|
C | A | 6 | a0002a0011a0014others(3): Show | 45 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(42): Show |
missense_variant | MODERATE | c.3853C>A | p.Gln1285Lys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3972/8014 | 3853/7806 | 1285/2601 | chr11 | 93698765 | ||
chr11:93698931
|
T | C | 1 | a0017 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.4019T>C | p.Ile1340Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4138/8014 | 4019/7806 | 1340/2601 | chr11 | 93698931 | ||
chr11:93699234
|
G | A | 2 | a0006a0017 | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.4322G>A | p.Gly1441Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4441/8014 | 4322/7806 | 1441/2601 | chr11 | 93699234 | ||
chr11:93699288
|
T | G | 4 | a0006a0009a0010others(1): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.4376T>G | p.Leu1459Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4495/8014 | 4376/7806 | 1459/2601 | chr11 | 93699288 | ||
chr11:93699692
|
A | C | 4 | a0006a0009a0010others(1): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.4780A>C | p.Lys1594Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4899/8014 | 4780/7806 | 1594/2601 | chr11 | 93699692 | ||
chr11:93699714
|
A | G | 1 | a0021 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.4802A>G | p.Asp1601Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4921/8014 | 4802/7806 | 1601/2601 | chr11 | 93699714 | ||
chr11:93699797
|
C | G | 1 | a0012 | 2 | NA19058.hp2 NA19077.hp1 |
missense_variant | MODERATE | c.4885C>G | p.Gln1629Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5004/8014 | 4885/7806 | 1629/2601 | chr11 | 93699797 | ||
chr11:93699798
|
A | G | 1 | a0030 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.4886A>G | p.Gln1629Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5005/8014 | 4886/7806 | 1629/2601 | chr11 | 93699798 | ||
chr11:93699858
|
A | C | 2 | a0006a0017 | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.4946A>C | p.Lys1649Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5065/8014 | 4946/7806 | 1649/2601 | chr11 | 93699858 | ||
chr11:93706835
|
C | T | 2 | a0022a0023 | 2 | NA18985.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.5687C>T | p.Pro1896Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/30 | 5806/8014 | 5687/7806 | 1896/2601 | chr11 | 93706835 | ||
chr11:93721377
|
G | A | 2 | a0006a0017 | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.5815G>A | p.Ala1939Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/30 | 5934/8014 | 5815/7806 | 1939/2601 | chr11 | 93721377 | ||
chr11:93724328
|
T | C | 1 | a0019 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.6271T>C | p.Ser2091Pro | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/30 | 6390/8014 | 6271/7806 | 2091/2601 | chr11 | 93724328 | ||
chr11:93724359
|
A | G | 1 | a0023 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.6302A>G | p.Asn2101Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/30 | 6421/8014 | 6302/7806 | 2101/2601 | chr11 | 93724359 | ||
chr11:93725777
|
A | G | 2 | a0006a0017 | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.6445A>G | p.Thr2149Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/30 | 6564/8014 | 6445/7806 | 2149/2601 | chr11 | 93725777 | ||
chr11:93726994
|
A | C | 7 | a0002a0004a0008others(4): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
missense_variant | MODERATE | c.6518A>C | p.Glu2173Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 6637/8014 | 6518/7806 | 2173/2601 | chr11 | 93726994 | ||
chr11:93727098
|
C | G | 1 | a0015 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.6622C>G | p.Gln2208Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 6741/8014 | 6622/7806 | 2208/2601 | chr11 | 93727098 | ||
chr11:93727477
|
T | C | 1 | a0026 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.7001T>C | p.Ile2334Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 7120/8014 | 7001/7806 | 2334/2601 | chr11 | 93727477 | ||
chr11:93727480
|
A | G | 1 | a0025 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.7004A>G | p.Gln2335Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 7123/8014 | 7004/7806 | 2335/2601 | chr11 | 93727480 | ||
chr11:93728681
|
G | GGGGGGGG others(37): Show |
1 | a0029 | 1 | NA18986.hp2 | frameshift_variant&splice_region_variant | HIGH | c.7162_7163insGGGGGG others(38): Show |
p.Glu2388fs | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7282/8014 | 7163/7806 | 2388/2601 | chr11 | 93728681 | ||
chr11:93728702
|
A | G | 1 | a0029 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.7183A>G | p.Ile2395Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7302/8014 | 7183/7806 | 2395/2601 | chr11 | 93728702 | ||
chr11:93728729
|
A | G | 3 | a0006a0009a0017 | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
missense_variant | MODERATE | c.7210A>G | p.Ile2404Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7329/8014 | 7210/7806 | 2404/2601 | chr11 | 93728729 | ||
chr11:93729441
|
A | T | 12 | a0001a0012a0015others(9): Show | 206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
missense_variant | MODERATE | c.7310A>T | p.Glu2437Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/30 | 7429/8014 | 7310/7806 | 2437/2601 | chr11 | 93729441 | ||
chr11:93729474
|
C | T | 1 | a0024 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.7343C>T | p.Ser2448Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/30 | 7462/8014 | 7343/7806 | 2448/2601 | chr11 | 93729474 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93667630
|
C | T | 9 | a0002c0002a0004c0005a0004c0043others(6): Show | 62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
synonymous_variant | LOW | c.132C>T | p.Ile44Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/30 | 251/8014 | 132/7806 | 44/2601 | chr11 | 93667630 | ||
chr11:93668840
|
A | G | 8 | a0002c0002a0004c0005a0004c0047others(5): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
synonymous_variant | LOW | c.342A>G | p.Ala114Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/30 | 461/8014 | 342/7806 | 114/2601 | chr11 | 93668840 | ||
chr11:93668930
|
C | A | 35 | a0001c0001a0001c0012a0001c0013others(32): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
splice_region_variant&synonymous_variant | LOW | c.432C>A | p.Thr144Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/30 | 551/8014 | 432/7806 | 144/2601 | chr11 | 93668930 | ||
chr11:93696865
|
C | G | 1 | a0005c0033 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1953C>G | p.Leu651Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2072/8014 | 1953/7806 | 651/2601 | chr11 | 93696865 | ||
chr11:93696943
|
G | A | 1 | a0009c0017 | 2 | HG01099.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.2031G>A | p.Ala677Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2150/8014 | 2031/7806 | 677/2601 | chr11 | 93696943 | ||
chr11:93697504
|
T | A | 5 | a0006c0004a0006c0037a0009c0017others(2): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.2592T>A | p.Thr864Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2711/8014 | 2592/7806 | 864/2601 | chr11 | 93697504 | ||
chr11:93697876
|
C | T | 5 | a0006c0004a0006c0037a0009c0017others(2): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.2964C>T | p.Ser988Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3083/8014 | 2964/7806 | 988/2601 | chr11 | 93697876 | ||
chr11:93697996
|
A | G | 1 | a0001c0032 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.3084A>G | p.Gly1028Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3203/8014 | 3084/7806 | 1028/2601 | chr11 | 93697996 | ||
chr11:93698794
|
G | A | 1 | a0004c0047 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.3882G>A | p.Gln1294Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4001/8014 | 3882/7806 | 1294/2601 | chr11 | 93698794 | ||
chr11:93698963
|
T | C | 1 | a0003c0010 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.4051T>C | p.Leu1351Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4170/8014 | 4051/7806 | 1351/2601 | chr11 | 93698963 | ||
chr11:93699199
|
C | T | 1 | a0001c0016 | 2 | NA19077.hp2 NA19080.hp2 |
synonymous_variant | LOW | c.4287C>T | p.Ser1429Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4406/8014 | 4287/7806 | 1429/2601 | chr11 | 93699199 | ||
chr11:93699430
|
G | A | 5 | a0006c0004a0006c0037a0009c0017others(2): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.4518G>A | p.Gln1506Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4637/8014 | 4518/7806 | 1506/2601 | chr11 | 93699430 | ||
chr11:93699520
|
A | G | 1 | a0003c0010 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.4608A>G | p.Glu1536Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4727/8014 | 4608/7806 | 1536/2601 | chr11 | 93699520 | ||
chr11:93699874
|
G | T | 1 | a0006c0037 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.4962G>T | p.Ser1654Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5081/8014 | 4962/7806 | 1654/2601 | chr11 | 93699874 | ||
chr11:93700096
|
G | A | 5 | a0006c0004a0006c0037a0009c0017others(2): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.5184G>A | p.Gln1728Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5303/8014 | 5184/7806 | 1728/2601 | chr11 | 93700096 | ||
chr11:93702471
|
C | T | 1 | a0005c0014 | 2 | HG02004.hp1 HG02280.hp2 |
synonymous_variant | LOW | c.5286C>T | p.Pro1762Pro | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 16/30 | 5405/8014 | 5286/7806 | 1762/2601 | chr11 | 93702471 | ||
chr11:93706776
|
C | G | 1 | a0001c0013 | 2 | HG03834.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.5628C>G | p.Pro1876Pro | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/30 | 5747/8014 | 5628/7806 | 1876/2601 | chr11 | 93706776 | ||
chr11:93721358
|
T | C | 3 | a0001c0012a0005c0011a0027c0023 | 5 | HG01255.hp1 HG01891.hp2 NA20805.hp2 others(2): Show |
synonymous_variant | LOW | c.5796T>C | p.Tyr1932Tyr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/30 | 5915/8014 | 5796/7806 | 1932/2601 | chr11 | 93721358 | ||
chr11:93725743
|
T | G | 1 | a0005c0026 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.6411T>G | p.Ser2137Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/30 | 6530/8014 | 6411/7806 | 2137/2601 | chr11 | 93725743 | ||
chr11:93727010
|
A | G | 3 | a0006c0004a0006c0037a0017c0036 | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
synonymous_variant | LOW | c.6534A>G | p.Glu2178Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 6653/8014 | 6534/7806 | 2178/2601 | chr11 | 93727010 | ||
chr11:93727481
|
G | A | 1 | a0025c0029 | 1 | NA19055.hp1 | synonymous_variant | LOW | c.7005G>A | p.Gln2335Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 7124/8014 | 7005/7806 | 2335/2601 | chr11 | 93727481 | ||
chr11:93728701
|
T | G | 1 | a0029c0039 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.7182T>G | p.Gly2394Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7301/8014 | 7182/7806 | 2394/2601 | chr11 | 93728701 | ||
chr11:93729729
|
T | C | 1 | a0003c0019 | 2 | NA19030.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.7515T>C | p.Ile2505Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 27/30 | 7634/8014 | 7515/7806 | 2505/2601 | chr11 | 93729729 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93661761
|
C | A | 1 | a0004c0005t0003 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/30 | 4947 | chr11 | 93661761 | |||||
chr11:93666690
|
T | C | 1 | a0030c0040t0004 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/30 | 18 | chr11 | 93666690 | |||||
chr11:93730330
|
T | G | 1 | a0009c0017t0002 | 2 | HG01099.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*61T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 30/30 | 61 | chr11 | 93730330 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93661890
|
A | C | 4 | a0009c0017t0002g0310a0009c0017t0002g0313a0010c0018t0001g0311others(1): Show | 4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+116A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93661890 | ||||||
chr11:93662020
|
G | C | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-27+246G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662020 | ||||||
chr11:93662155
|
G | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27+381G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662155 | ||||||
chr11:93662307
|
G | A | 1 | a0005c0006t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-27+533G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662307 | ||||||
chr11:93662356
|
G | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-27+582G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662356 | ||||||
chr11:93662650
|
T | C | 2 | a0004c0009t0001g0037a0004c0009t0001g0038 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-27+876T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662650 | ||||||
chr11:93662748
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-27+974A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662748 | ||||||
chr11:93662883
|
A | G | 4 | a0003c0003t0001g0025a0003c0003t0001g0308a0003c0003t0001g0309others(1): Show | 5 | NA18953.hp1 NA18968.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+1109A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662883 | ||||||
chr11:93663011
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0277 | 3 | NA18966.hp2 NA18990.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-27+1237A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663011 | ||||||
chr11:93663043
|
G | A | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-27+1269G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663043 | ||||||
chr11:93663267
|
T | C | 1 | a0031c0038t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-27+1493T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663267 | ||||||
chr11:93663296
|
C | A | 3 | a0005c0006t0001g0040a0005c0006t0001g0042a0024c0028t0001g0041 | 3 | HG02109.hp2 HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-27+1522C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663296 | ||||||
chr11:93663521
|
T | C | 2 | a0005c0006t0001g0043a0005c0006t0001g0044 | 2 | HG00741.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-27+1747T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663521 | ||||||
chr11:93663660
|
T | C | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-27+1886T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663660 | ||||||
chr11:93664192
|
CA | C | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27+2419delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664192 | ||||||
chr11:93664334
|
G | C | 18 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(15): Show | 21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26-2348G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664334 | ||||||
chr11:93664373
|
G | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0260others(13): Show | 19 | HG00438.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-2309G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664373 | ||||||
chr11:93664415
|
G | A | 1 | a0031c0038t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-26-2267G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664415 | ||||||
chr11:93664451
|
C | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-26-2231C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664451 | ||||||
chr11:93664473
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-2209C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664473 | ||||||
chr11:93664658
|
C | T | 1 | a0001c0032t0001g0254 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-26-2024C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664658 | ||||||
chr11:93664676
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-26-2006C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664676 | ||||||
chr11:93664824
|
C | T | 1 | a0004c0047t0001g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-26-1858C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664824 | ||||||
chr11:93664836
|
G | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-26-1846G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664836 | ||||||
chr11:93665131
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-26-1551A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665131 | ||||||
chr11:93665407
|
C | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-1275C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665407 | ||||||
chr11:93665430
|
G | A | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(259): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-26-1252G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665430 | ||||||
chr11:93665477
|
G | T | 1 | a0004c0005t0001g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-26-1205G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665477 | ||||||
chr11:93665639
|
C | T | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-26-1043C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665639 | ||||||
chr11:93665721
|
A | G | 1 | a0009c0017t0002g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-26-961A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665721 | ||||||
chr11:93665740
|
C | T | 4 | a0009c0017t0002g0310a0009c0017t0002g0313a0010c0018t0001g0311others(1): Show | 4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-942C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665740 | ||||||
chr11:93665944
|
T | C | 20 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(17): Show | 20 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-26-738T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665944 | ||||||
chr11:93665994
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-26-688T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665994 | ||||||
chr11:93666019
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-26-663G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666019 | ||||||
chr11:93666212
|
C | T | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-26-470C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666212 | ||||||
chr11:93666214
|
A | G | 1 | a0001c0032t0001g0254 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-26-468A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666214 | ||||||
chr11:93666232
|
C | T | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-26-450C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666232 | ||||||
chr11:93666236
|
G | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-446G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666236 | ||||||
chr11:93666401
|
C | G | 1 | a0028c0022t0001g0250 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-26-281C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666401 | ||||||
chr11:93666519
|
G | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-163G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666519 | ||||||
chr11:93666599
|
A | C | 1 | a0001c0001t0001g0249 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-26-83A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666599 | ||||||
chr11:93666650
|
A | AT | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-27dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr11 | 93666650 | |||||
chr11:93666832
|
A | G | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+17A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666832 | ||||||
chr11:93666837
|
G | A | 3 | a0006c0004t0001g0027a0006c0004t0001g0029a0006c0037t0001g0028 | 3 | NA18969.hp1 NA18997.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.108+22G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666837 | ||||||
chr11:93666886
|
G | A | 300 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(297): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.108+71G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666886 | ||||||
chr11:93666940
|
A | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.108+125A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666940 | ||||||
chr11:93667016
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG01256.hp1 HG02145.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.108+201T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667016 | ||||||
chr11:93667054
|
A | G | 1 | a0003c0010t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.108+239A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667054 | ||||||
chr11:93667111
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.108+296T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667111 | ||||||
chr11:93667137
|
T | C | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+322T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667137 | ||||||
chr11:93667337
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.109-270G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667337 | ||||||
chr11:93668000
|
TC | T | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.309+195delC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr11 | 93668000 | |||||
chr11:93668027
|
A | G | 97 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 101 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.309+220A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668027 | ||||||
chr11:93668242
|
C | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.309+435C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668242 | ||||||
chr11:93668426
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.310-382A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668426 | ||||||
chr11:93668452
|
CA | C | 3 | a0005c0011t0001g0246a0005c0011t0001g0248a0027c0023t0001g0247 | 3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.310-354delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr11 | 93668452 | |||||
chr11:93668454
|
A | G | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.310-354A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668454 | ||||||
chr11:93668525
|
C | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.310-283C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668525 | ||||||
chr11:93668649
|
A | G | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.310-159A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668649 | ||||||
chr11:93668653
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(53): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.310-155C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668653 | ||||||
chr11:93669260
|
G | A | 3 | a0003c0003t0001g0023a0003c0003t0001g0293a0003c0003t0001g0294 | 4 | HG01891.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+328G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | chr11 | 93669260 | ||||||
chr11:93669414
|
G | GT | 166 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(163): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.435-250dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr11 | 93669414 | |||||
chr11:93669469
|
C | G | 2 | a0005c0006t0001g0043a0005c0006t0001g0044 | 2 | HG00741.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-208C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | chr11 | 93669469 | ||||||
chr11:93669527
|
A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.435-150A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | chr11 | 93669527 | ||||||
chr11:93669779
|
G | A | 18 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(15): Show | 21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.528+9G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669779 | ||||||
chr11:93669901
|
G | A | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.528+131G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669901 | ||||||
chr11:93669932
|
A | G | 1 | a0009c0017t0002g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.528+162A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669932 | ||||||
chr11:93669945
|
T | C | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.528+175T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669945 | ||||||
chr11:93670180
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+410C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670180 | ||||||
chr11:93670268
|
A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+498A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670268 | ||||||
chr11:93670323
|
T | A | 91 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 95 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.528+553T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670323 | ||||||
chr11:93670397
|
T | A | 2 | a0003c0010t0001g0022a0003c0010t0001g0292 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.528+627T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670397 | ||||||
chr11:93670397
|
TA | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+634delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93670397 | |||||
chr11:93670710
|
G | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.528+940G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670710 | ||||||
chr11:93670812
|
A | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+1042A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670812 | ||||||
chr11:93670888
|
CT | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.528+1125delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93670888 | |||||
chr11:93670895
|
T | G | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.528+1125T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670895 | ||||||
chr11:93670968
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+1198T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670968 | ||||||
chr11:93670985
|
C | T | 1 | a0003c0003t0001g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.528+1215C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670985 | ||||||
chr11:93671046
|
C | G | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.528+1276C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671046 | ||||||
chr11:93671111
|
G | C | 5 | a0007c0007t0001g0072a0007c0007t0001g0073a0007c0007t0001g0075others(2): Show | 5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+1341G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671111 | ||||||
chr11:93671315
|
C | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG00140.hp2 HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.528+1545C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671315 | ||||||
chr11:93671353
|
T | C | 5 | a0007c0007t0001g0072a0007c0007t0001g0073a0007c0007t0001g0075others(2): Show | 5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+1583T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671353 | ||||||
chr11:93671442
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.528+1672C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671442 | ||||||
chr11:93671458
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.528+1688G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671458 | ||||||
chr11:93671758
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.528+1988G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671758 | ||||||
chr11:93671771
|
A | G | 1 | a0009c0017t0002g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.528+2001A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671771 | ||||||
chr11:93671773
|
G | T | 3 | a0005c0006t0001g0062a0015c0035t0001g0061a0016c0034t0001g0060 | 3 | HG01109.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.528+2003G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671773 | ||||||
chr11:93671774
|
C | T | 3 | a0005c0006t0001g0062a0015c0035t0001g0061a0016c0034t0001g0060 | 3 | HG01109.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.528+2004C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671774 | ||||||
chr11:93671909
|
G | A | 1 | a0003c0003t0001g0295 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.528+2139G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671909 | ||||||
chr11:93671965
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.528+2195G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671965 | ||||||
chr11:93672124
|
T | C | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.528+2354T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672124 | ||||||
chr11:93672216
|
C | T | 1 | a0003c0003t0001g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.528+2446C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672216 | ||||||
chr11:93672253
|
A | G | 2 | a0004c0005t0003g0026a0004c0047t0001g0253 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.528+2483A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672253 | ||||||
chr11:93672356
|
G | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+2586G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672356 | ||||||
chr11:93672416
|
C | CT | 16 | a0005c0026t0001g0045a0006c0004t0001g0002a0006c0004t0001g0027others(13): Show | 19 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.528+2659dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93672416 | |||||
chr11:93672435
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.528+2665G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672435 | ||||||
chr11:93672567
|
A | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+2797A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672567 | ||||||
chr11:93672670
|
A | G | 2 | a0003c0010t0001g0022a0003c0010t0001g0292 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.528+2900A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672670 | ||||||
chr11:93672734
|
A | C | 1 | a0031c0038t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.529-2837A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672734 | ||||||
chr11:93672832
|
TATAATC | T | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.529-2737_529-2732d others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93672832 | |||||
chr11:93672897
|
A | C | 17 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(14): Show | 17 | HG00140.hp2 HG01099.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.529-2674A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672897 | ||||||
chr11:93672932
|
G | GGTACTTT others(4): Show |
1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.529-2630_529-2629i others(13): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93672932 | |||||
chr11:93672949
|
A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.529-2622A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672949 | ||||||
chr11:93672981
|
C | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.529-2590C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672981 | ||||||
chr11:93673116
|
T | A | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.529-2455T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673116 | ||||||
chr11:93673199
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.529-2372T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673199 | ||||||
chr11:93673238
|
C | G | 1 | a0018c0024t0001g0172 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.529-2333C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673238 | ||||||
chr11:93673451
|
A | G | 1 | a0032c0041t0001g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.529-2120A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673451 | ||||||
chr11:93673481
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.529-2090T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673481 | ||||||
chr11:93673543
|
G | T | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.529-2028G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673543 | ||||||
chr11:93673597
|
G | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.529-1974G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673597 | ||||||
chr11:93673603
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.529-1968C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673603 | ||||||
chr11:93673689
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.529-1882C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673689 | ||||||
chr11:93673784
|
C | T | 300 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(297): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.529-1787C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673784 | ||||||
chr11:93673848
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0277 | 3 | NA18966.hp2 NA18990.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.529-1723C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673848 | ||||||
chr11:93673943
|
T | TC | 224 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(221): Show | 246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.529-1622dupC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93673943 | |||||
chr11:93673950
|
T | C | 56 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0185others(53): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.529-1621T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673950 | ||||||
chr11:93673952
|
C | T | 56 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0185others(53): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.529-1619C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673952 | ||||||
chr11:93673953
|
T | C | 56 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0185others(53): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.529-1618T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673953 | ||||||
chr11:93673991
|
C | T | 1 | a0005c0006t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.529-1580C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673991 | ||||||
chr11:93674051
|
C | T | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.529-1520C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674051 | ||||||
chr11:93674087
|
C | T | 1 | a0028c0022t0001g0250 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.529-1484C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674087 | ||||||
chr11:93674225
|
A | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.529-1346A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674225 | ||||||
chr11:93674252
|
C | T | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.529-1319C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674252 | ||||||
chr11:93674496
|
A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.529-1075A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674496 | ||||||
chr11:93674603
|
A | T | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.529-968A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674603 | ||||||
chr11:93674676
|
T | G | 4 | a0009c0017t0002g0310a0009c0017t0002g0313a0010c0018t0001g0311others(1): Show | 4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-895T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674676 | ||||||
chr11:93674682
|
G | GT | 11 | a0001c0001t0001g0016a0001c0001t0001g0233a0001c0001t0001g0234others(8): Show | 12 | HG01109.hp2 HG01192.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.529-885dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93674682 | |||||
chr11:93674773
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.529-798T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674773 | ||||||
chr11:93674775
|
C | T | 1 | a0032c0041t0001g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.529-796C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674775 | ||||||
chr11:93674783
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.529-788A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674783 | ||||||
chr11:93674789
|
T | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-782T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674789 | ||||||
chr11:93674877
|
G | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.529-694G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674877 | ||||||
chr11:93674918
|
A | G | 52 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(49): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.529-653A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674918 | ||||||
chr11:93675161
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.529-410C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93675161 | ||||||
chr11:93675318
|
T | TA | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.529-248dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93675318 | |||||
chr11:93675438
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.529-133A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93675438 | ||||||
chr11:93675562
|
CTT | C | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.529-6_529-5delTT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93675562 | |||||
chr11:93675792
|
C | CA | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.624+130dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr11 | 93675792 | |||||
chr11:93676025
|
A | G | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.624+359A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676025 | ||||||
chr11:93676049
|
A | G | 2 | a0005c0006t0001g0042a0024c0028t0001g0041 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.624+383A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676049 | ||||||
chr11:93676107
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.624+441A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676107 | ||||||
chr11:93676174
|
C | T | 4 | a0004c0009t0001g0037a0004c0009t0001g0038a0004c0009t0001g0124others(1): Show | 4 | HG02055.hp1 HG03130.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+508C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676174 | ||||||
chr11:93676282
|
A | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.624+616A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676282 | ||||||
chr11:93676396
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.624+730A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676396 | ||||||
chr11:93676448
|
C | T | 2 | a0003c0019t0001g0288a0003c0019t0001g0289 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.624+782C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676448 | ||||||
chr11:93676608
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18953.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.624+942A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676608 | ||||||
chr11:93676613
|
T | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0260others(13): Show | 19 | HG00438.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.624+947T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676613 | ||||||
chr11:93676638
|
G | A | 300 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(297): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.624+972G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676638 | ||||||
chr11:93676685
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.624+1019T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676685 | ||||||
chr11:93676692
|
C | G | 1 | a0010c0018t0001g0312 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.624+1026C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676692 | ||||||
chr11:93676815
|
A | T | 1 | a0002c0002t0001g0123 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.624+1149A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676815 | ||||||
chr11:93676879
|
G | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.624+1213G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676879 | ||||||
chr11:93676918
|
G | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.624+1252G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676918 | ||||||
chr11:93677132
|
C | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.624+1466C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677132 | ||||||
chr11:93677190
|
T | C | 3 | a0004c0009t0001g0037a0004c0009t0001g0038a0004c0009t0001g0124 | 3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.624+1524T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677190 | ||||||
chr11:93677370
|
A | G | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.624+1704A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677370 | ||||||
chr11:93677414
|
A | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+1748A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677414 | ||||||
chr11:93677521
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.624+1855C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677521 | ||||||
chr11:93677560
|
C | T | 1 | a0008c0008t0001g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.625-1852C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677560 | ||||||
chr11:93677694
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.625-1718G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677694 | ||||||
chr11:93677987
|
A | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.625-1425A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677987 | ||||||
chr11:93678083
|
T | A | 1 | a0014c0044t0001g0081 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.625-1329T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678083 | ||||||
chr11:93678097
|
T | C | 1 | a0005c0006t0001g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.625-1315T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678097 | ||||||
chr11:93678292
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.625-1120C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678292 | ||||||
chr11:93678665
|
C | T | 1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.625-747C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678665 | ||||||
chr11:93678681
|
G | A | 1 | a0002c0002t0001g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.625-731G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678681 | ||||||
chr11:93678733
|
G | A | 97 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 101 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.625-679G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678733 | ||||||
chr11:93678880
|
G | A | 17 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(14): Show | 20 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.625-532G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678880 | ||||||
chr11:93678882
|
A | T | 2 | a0003c0010t0001g0022a0003c0010t0001g0292 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.625-530A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678882 | ||||||
chr11:93679046
|
A | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.625-366A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679046 | ||||||
chr11:93679232
|
A | C | 1 | a0014c0044t0001g0081 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.625-180A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679232 | ||||||
chr11:93679267
|
C | T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-145C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679267 | ||||||
chr11:93679329
|
T | A | 1 | a0014c0044t0001g0081 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.625-83T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679329 | ||||||
chr11:93679364
|
T | C | 7 | a0003c0003t0001g0024a0003c0003t0001g0295a0003c0003t0001g0296others(4): Show | 8 | HG01074.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.625-48T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679364 | ||||||
chr11:93679408
|
C | G | 1 | a0030c0040t0004g0300 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.625-4C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679408 | ||||||
chr11:93679563
|
T | C | 5 | a0004c0005t0001g0086a0008c0008t0001g0083a0008c0008t0001g0084others(2): Show | 5 | HG02451.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.765+11T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679563 | ||||||
chr11:93679608
|
A | G | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.765+56A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679608 | ||||||
chr11:93679660
|
T | C | 53 | a0001c0001t0001g0127a0002c0002t0001g0001a0002c0002t0001g0005others(50): Show | 62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.765+108T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679660 | ||||||
chr11:93679892
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.765+340T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679892 | ||||||
chr11:93679967
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.765+415C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679967 | ||||||
chr11:93680005
|
G | A | 2 | a0005c0006t0001g0274a0005c0006t0001g0275 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.765+453G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680005 | ||||||
chr11:93680201
|
C | T | 3 | a0001c0001t0001g0183a0003c0010t0001g0022a0003c0010t0001g0292 | 4 | HG01884.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+649C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680201 | ||||||
chr11:93680287
|
A | G | 1 | a0008c0008t0001g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.765+735A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680287 | ||||||
chr11:93680319
|
C | T | 3 | a0003c0019t0001g0288a0003c0019t0001g0289a0032c0041t0001g0290 | 3 | HG02723.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.765+767C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680319 | ||||||
chr11:93680537
|
T | C | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.765+985T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680537 | ||||||
chr11:93680655
|
C | A | 7 | a0003c0003t0001g0024a0003c0003t0001g0295a0003c0003t0001g0296others(4): Show | 8 | HG01074.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.765+1103C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680655 | ||||||
chr11:93680691
|
G | A | 300 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(297): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.765+1139G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680691 | ||||||
chr11:93680796
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.765+1244A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680796 | ||||||
chr11:93681004
|
G | A | 4 | a0008c0008t0001g0083a0008c0008t0001g0084a0008c0008t0001g0085others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+1452G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681004 | ||||||
chr11:93681090
|
C | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.765+1538C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681090 | ||||||
chr11:93681141
|
A | G | 2 | a0015c0035t0001g0061a0016c0034t0001g0060 | 2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.765+1589A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681141 | ||||||
chr11:93681235
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765+1683T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681235 | ||||||
chr11:93681237
|
GT | G | 170 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 186 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.765+1702delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681237 | |||||
chr11:93681240
|
T | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(106): Show | 124 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.765+1688T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681240 | ||||||
chr11:93681241
|
T | G | 170 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 186 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.765+1689T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681241 | ||||||
chr11:93681242
|
T | G | 1 | a0014c0044t0001g0081 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.765+1690T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681242 | ||||||
chr11:93681276
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 6 | NA18971.hp1 NA18972.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.765+1724G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681276 | ||||||
chr11:93681403
|
A | AT | 19 | a0003c0003t0001g0020a0003c0003t0001g0025a0003c0003t0001g0281others(16): Show | 24 | HG01074.hp2 HG01361.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.765+1881dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
A | ATT | 41 | a0001c0001t0001g0071a0001c0001t0001g0190a0002c0002t0001g0001others(38): Show | 51 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.765+1880_765+1881d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
A | ATTT | 65 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0069others(62): Show | 67 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.765+1879_765+1881d others(5): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
A | ATTTT | 61 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(58): Show | 63 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.765+1878_765+1881d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
A | ATTTTT | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(47): Show | 61 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.765+1877_765+1881d others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
A | ATTTTTT | 46 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(43): Show | 50 | HG00438.hp1 HG00741.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.765+1876_765+1881d others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
A | ATTTTTTT | 12 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 12 | HG01099.hp2 HG01358.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+1875_765+1881d others(9): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.765+1872_765+1881d others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681403
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.765+1871_765+1881d others(13): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | |||||
chr11:93681463
|
G | T | 298 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(295): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.765+1911G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681463 | ||||||
chr11:93681472
|
A | G | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(278): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.765+1920A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681472 | ||||||
chr11:93681477
|
G | A | 7 | a0003c0003t0001g0280a0005c0006t0001g0040a0005c0006t0001g0042others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.765+1925G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681477 | ||||||
chr11:93681517
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.765+1965A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681517 | ||||||
chr11:93681693
|
C | T | 1 | a0023c0031t0001g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.766-1866C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681693 | ||||||
chr11:93681786
|
A | G | 1 | a0027c0023t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.766-1773A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681786 | ||||||
chr11:93681860
|
G | GT | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(187): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.766-1687dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681860 | |||||
chr11:93681865
|
T | TG | 90 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.766-1694_766-1693i others(3): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681865 | ||||||
chr11:93681920
|
A | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.766-1639A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681920 | ||||||
chr11:93681921
|
A | G | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.766-1638A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681921 | ||||||
chr11:93681924
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02922.hp2 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.766-1635A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681924 | ||||||
chr11:93682127
|
A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.766-1432A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682127 | ||||||
chr11:93682458
|
A | G | 2 | a0011c0020t0001g0087a0011c0020t0001g0102 | 2 | HG02683.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.766-1101A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682458 | ||||||
chr11:93682538
|
T | A | 1 | a0003c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-1021T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682538 | ||||||
chr11:93682596
|
TA | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(98): Show | 116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.766-952delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93682596 | |||||
chr11:93682674
|
A | T | 69 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(66): Show | 72 | HG00323.hp2 HG00438.hp2 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.766-885A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682674 | ||||||
chr11:93682821
|
C | T | 1 | a0004c0005t0001g0101 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.766-738C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682821 | ||||||
chr11:93683059
|
T | G | 18 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(15): Show | 21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.766-500T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683059 | ||||||
chr11:93683142
|
C | T | 1 | a0005c0011t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766-417C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683142 | ||||||
chr11:93683305
|
C | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0216others(1): Show | 4 | HG02148.hp1 HG02257.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-254C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683305 | ||||||
chr11:93683346
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.766-213A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683346 | ||||||
chr11:93683367
|
G | T | 1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-192G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683367 | ||||||
chr11:93683495
|
C | T | 1 | a0003c0003t0001g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.766-64C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683495 | ||||||
chr11:93683797
|
A | G | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.949+55A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 8/29 | chr11 | 93683797 | ||||||
chr11:93683948
|
A | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.950-16A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 8/29 | chr11 | 93683948 | ||||||
chr11:93684145
|
G | A | 2 | a0015c0035t0001g0061a0016c0034t0001g0060 | 2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1114+17G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684145 | ||||||
chr11:93684271
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1114+143C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684271 | ||||||
chr11:93684294
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(53): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1114+166C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684294 | ||||||
chr11:93684295
|
G | A | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1114+167G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684295 | ||||||
chr11:93684343
|
G | C | 1 | a0004c0005t0001g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1114+215G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684343 | ||||||
chr11:93684624
|
G | A | 1 | a0004c0005t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1114+496G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684624 | ||||||
chr11:93684638
|
G | A | 3 | a0003c0003t0001g0021a0003c0003t0001g0281a0003c0003t0001g0291 | 4 | HG01081.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+510G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684638 | ||||||
chr11:93684693
|
C | T | 91 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 95 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1114+565C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684693 | ||||||
chr11:93684809
|
C | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0224 | 3 | HG01516.hp2 HG01943.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1114+681C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684809 | ||||||
chr11:93684848
|
G | A | 307 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(304): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1114+720G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684848 | ||||||
chr11:93684898
|
C | T | 1 | a0005c0006t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1114+770C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684898 | ||||||
chr11:93684965
|
T | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | NA18941.hp2 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1114+837T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684965 | ||||||
chr11:93685028
|
A | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1114+900A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685028 | ||||||
chr11:93685200
|
A | G | 1 | a0005c0006t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1114+1072A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685200 | ||||||
chr11:93685231
|
T | C | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1114+1103T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685231 | ||||||
chr11:93685366
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1114+1238C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685366 | ||||||
chr11:93685398
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0243 | 2 | NA18988.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1114+1270G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685398 | ||||||
chr11:93685403
|
C | T | 47 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(44): Show | 56 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.1114+1275C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685403 | ||||||
chr11:93685525
|
A | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1114+1397A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685525 | ||||||
chr11:93685531
|
A | C | 1 | a0005c0006t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1114+1403A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685531 | ||||||
chr11:93685538
|
G | GA | 7 | a0003c0003t0001g0024a0003c0003t0001g0295a0003c0003t0001g0296others(4): Show | 8 | HG01074.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114+1418dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685538 | |||||
chr11:93685575
|
T | A | 1 | a0004c0005t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1114+1447T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685575 | ||||||
chr11:93685593
|
A | G | 298 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(295): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1114+1465A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685593 | ||||||
chr11:93685609
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1114+1481A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685609 | ||||||
chr11:93685686
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1114+1558C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685686 | ||||||
chr11:93685700
|
C | CTTTG | 149 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(146): Show | 161 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1114+1596_1114+159 others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685700 | |||||
chr11:93685700
|
C | CTTTGTTT others(1): Show |
112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(109): Show | 128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1114+1592_1114+159 others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685700 | |||||
chr11:93685700
|
C | CTTTGTTT others(5): Show |
4 | a0001c0001t0001g0135a0001c0001t0001g0168a0001c0001t0001g0237others(1): Show | 4 | NA19011.hp1 NA19057.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+1588_1114+159 others(16): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685700 | |||||
chr11:93685774
|
G | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.1114+1646G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685774 | ||||||
chr11:93685804
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1114+1676G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685804 | ||||||
chr11:93685841
|
G | GAGAGATT others(885): Show |
6 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1713_1114+171 others(896): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685841 | ||||||
chr11:93685844
|
G | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1716G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685844 | ||||||
chr11:93685845
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1717G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685845 | ||||||
chr11:93685847
|
A | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1719A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685847 | ||||||
chr11:93685849
|
TACA | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1722_1114+172 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685849 | ||||||
chr11:93685853
|
G | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1725G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685853 | ||||||
chr11:93685931
|
G | A | 1 | a0004c0009t0001g0037 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1115-1713G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685931 | ||||||
chr11:93685949
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1115-1695C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685949 | ||||||
chr11:93686229
|
T | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1115-1415T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686229 | ||||||
chr11:93686288
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1115-1356C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686288 | ||||||
chr11:93686319
|
T | TA | 301 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(298): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1115-1313dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93686319 | |||||
chr11:93686319
|
T | TAA | 14 | a0001c0001t0001g0229a0002c0002t0001g0120a0005c0026t0001g0045others(11): Show | 17 | HG02165.hp1 HG03098.hp2 HG03453.hp1 others(14): Show |
intron_variant | MODIFIER | c.1115-1314_1115-131 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93686319 | |||||
chr11:93686337
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1115-1307T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686337 | ||||||
chr11:93686352
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1115-1292C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686352 | ||||||
chr11:93686665
|
A | G | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1115-979A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686665 | ||||||
chr11:93686682
|
A | G | 5 | a0005c0033t0001g0039a0009c0017t0002g0310a0009c0017t0002g0313others(2): Show | 5 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1115-962A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686682 | ||||||
chr11:93686796
|
T | C | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1115-848T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686796 | ||||||
chr11:93686953
|
T | G | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1115-691T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686953 | ||||||
chr11:93687156
|
C | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1115-488C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687156 | ||||||
chr11:93687194
|
C | T | 1 | a0031c0038t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1115-450C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687194 | ||||||
chr11:93687218
|
A | T | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1115-426A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687218 | ||||||
chr11:93687379
|
A | G | 1 | a0005c0006t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1115-265A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687379 | ||||||
chr11:93687399
|
A | G | 52 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(49): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1115-245A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687399 | ||||||
chr11:93687525
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1115-119G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687525 | ||||||
chr11:93688335
|
A | G | 1 | a0005c0011t0001g0248 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1336+470A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688335 | ||||||
chr11:93688399
|
T | G | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1336+534T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688399 | ||||||
chr11:93688434
|
G | A | 5 | a0007c0007t0001g0072a0007c0007t0001g0073a0007c0007t0001g0075others(2): Show | 5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+569G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688434 | ||||||
chr11:93688460
|
A | G | 1 | a0023c0031t0001g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1336+595A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688460 | ||||||
chr11:93688533
|
C | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1336+668C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688533 | ||||||
chr11:93688577
|
TG | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1336+714delG | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93688577 | |||||
chr11:93688593
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0129a0001c0001t0001g0160others(1): Show | 6 | HG02080.hp1 NA18942.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336+728C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688593 | ||||||
chr11:93688616
|
G | A | 91 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 95 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1336+751G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688616 | ||||||
chr11:93688644
|
A | C | 1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1336+779A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688644 | ||||||
chr11:93688671
|
C | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1336+806C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688671 | ||||||
chr11:93688681
|
C | T | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1336+816C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688681 | ||||||
chr11:93688984
|
G | C | 1 | a0002c0002t0001g0079 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1336+1119G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688984 | ||||||
chr11:93688999
|
T | C | 3 | a0004c0009t0001g0037a0004c0009t0001g0038a0004c0009t0001g0124 | 3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1336+1134T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688999 | ||||||
chr11:93689204
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0280a0003c0003t0001g0283others(1): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+1339A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689204 | ||||||
chr11:93689286
|
G | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1336+1421G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689286 | ||||||
chr11:93689447
|
G | A | 89 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(86): Show | 93 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1336+1582G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689447 | ||||||
chr11:93689545
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1336+1680A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689545 | ||||||
chr11:93689886
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1337-1797G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689886 | ||||||
chr11:93690071
|
G | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1337-1612G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690071 | ||||||
chr11:93690267
|
C | T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1337-1416C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690267 | ||||||
chr11:93690299
|
C | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1337-1384C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690299 | ||||||
chr11:93690431
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1337-1252T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690431 | ||||||
chr11:93690513
|
C | T | 5 | a0007c0007t0001g0072a0007c0007t0001g0073a0007c0007t0001g0075others(2): Show | 5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1337-1170C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690513 | ||||||
chr11:93690519
|
A | G | 4 | a0009c0017t0002g0310a0009c0017t0002g0313a0010c0018t0001g0311others(1): Show | 4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1337-1164A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690519 | ||||||
chr11:93690553
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1337-1130T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690553 | ||||||
chr11:93690560
|
C | CA | 26 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0066others(23): Show | 26 | HG01168.hp2 HG01169.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.1337-1102dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690560 | |||||
chr11:93690560
|
CA | C | 47 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(44): Show | 56 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.1337-1102delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690560 | |||||
chr11:93690635
|
G | A | 1 | a0002c0002t0001g0107 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1337-1048G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690635 | ||||||
chr11:93690729
|
C | CA | 8 | a0002c0002t0001g0090a0003c0003t0001g0024a0003c0003t0001g0295others(5): Show | 9 | HG00609.hp2 HG01074.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1337-930dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690729 | |||||
chr11:93690729
|
CA | C | 57 | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0069others(54): Show | 63 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.1337-930delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690729 | |||||
chr11:93690729
|
CAA | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1337-931_1337-930d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690729 | |||||
chr11:93690752
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1337-931A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690752 | ||||||
chr11:93690851
|
T | C | 1 | a0003c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1337-832T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690851 | ||||||
chr11:93690874
|
T | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1337-809T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690874 | ||||||
chr11:93690878
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1337-805C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690878 | ||||||
chr11:93690895
|
T | C | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1337-788T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690895 | ||||||
chr11:93691018
|
G | A | 4 | a0003c0003t0001g0020a0003c0003t0001g0280a0003c0003t0001g0283others(1): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1337-665G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691018 | ||||||
chr11:93691069
|
T | C | 1 | a0028c0022t0001g0250 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1337-614T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691069 | ||||||
chr11:93691103
|
T | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1337-580T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691103 | ||||||
chr11:93691113
|
A | T | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1337-570A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691113 | ||||||
chr11:93691181
|
T | TCTGC | 18 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(15): Show | 21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1337-500_1337-497d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93691181 | |||||
chr11:93691277
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG02148.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1337-406G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691277 | ||||||
chr11:93691288
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1337-395C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691288 | ||||||
chr11:93691478
|
A | G | 4 | a0005c0006t0001g0040a0005c0006t0001g0274a0005c0006t0001g0275others(1): Show | 4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1337-205A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691478 | ||||||
chr11:93691503
|
A | G | 1 | a0001c0013t0001g0209 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1337-180A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691503 | ||||||
chr11:93692173
|
A | AT | 7 | a0005c0014t0001g0077a0005c0014t0001g0078a0007c0007t0001g0072others(4): Show | 7 | HG02004.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533+144dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692173 | |||||
chr11:93692199
|
A | G | 1 | a0005c0014t0001g0077 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1533+169A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692199 | ||||||
chr11:93692232
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1533+202T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692232 | ||||||
chr11:93692426
|
A | G | 2 | a0015c0035t0001g0061a0016c0034t0001g0060 | 2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1533+396A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692426 | ||||||
chr11:93692482
|
G | A | 1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533+452G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692482 | ||||||
chr11:93692498
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0152 | 2 | NA18962.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1533+468G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692498 | ||||||
chr11:93692689
|
T | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0069others(16): Show | 20 | HG00408.hp2 HG00621.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1533+659T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692689 | ||||||
chr11:93692920
|
T | TC | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1533+891dupC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692920 | |||||
chr11:93692942
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1533+912C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692942 | ||||||
chr11:93692972
|
C | CA | 11 | a0001c0001t0001g0053a0001c0001t0001g0160a0001c0001t0001g0232others(8): Show | 11 | HG02055.hp1 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533+960dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692972 | |||||
chr11:93692972
|
CA | C | 14 | a0001c0001t0001g0134a0001c0001t0001g0235a0003c0019t0001g0288others(11): Show | 17 | HG01168.hp2 HG02165.hp1 NA18940.hp2 others(14): Show |
intron_variant | MODIFIER | c.1533+960delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692972 | |||||
chr11:93692983
|
A | C | 52 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(49): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1533+953A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692983 | ||||||
chr11:93693104
|
CG | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533+1075delG | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693104 | ||||||
chr11:93693106
|
T | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533+1076T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693106 | ||||||
chr11:93693145
|
C | T | 1 | a0003c0003t0001g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1533+1115C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693145 | ||||||
chr11:93693149
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533+1119C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693149 | ||||||
chr11:93693193
|
T | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1533+1163T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693193 | ||||||
chr11:93693230
|
T | C | 2 | a0002c0002t0001g0082a0002c0002t0001g0108 | 2 | NA18991.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1533+1200T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693230 | ||||||
chr11:93693234
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1533+1204G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693234 | ||||||
chr11:93693288
|
A | G | 1 | a0003c0003t0001g0305 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1533+1258A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693288 | ||||||
chr11:93693354
|
C | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1533+1324C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693354 | ||||||
chr11:93693492
|
A | G | 1 | a0003c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1533+1462A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693492 | ||||||
chr11:93693495
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533+1465T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693495 | ||||||
chr11:93693542
|
G | C | 1 | a0005c0006t0001g0276 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1533+1512G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693542 | ||||||
chr11:93693585
|
A | C | 1 | a0028c0022t0001g0250 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1533+1555A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693585 | ||||||
chr11:93693616
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533+1586C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693616 | ||||||
chr11:93693687
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1533+1657T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693687 | ||||||
chr11:93693720
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1533+1690C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693720 | ||||||
chr11:93693787
|
C | G | 3 | a0003c0003t0001g0024a0003c0003t0001g0296a0003c0003t0001g0297 | 4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-1710C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693787 | ||||||
chr11:93693972
|
A | G | 1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1534-1525A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693972 | ||||||
chr11:93694127
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1534-1370G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694127 | ||||||
chr11:93694291
|
A | G | 2 | a0003c0010t0001g0022a0003c0010t0001g0292 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1534-1206A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694291 | ||||||
chr11:93694302
|
G | A | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1534-1195G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694302 | ||||||
chr11:93694422
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1534-1075A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694422 | ||||||
chr11:93694710
|
A | G | 1 | a0007c0007t0001g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1534-787A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694710 | ||||||
chr11:93694721
|
G | A | 15 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(12): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.1534-776G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694721 | ||||||
chr11:93694775
|
T | C | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.1534-722T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694775 | ||||||
chr11:93695125
|
A | T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1534-372A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695125 | ||||||
chr11:93695341
|
T | C | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1534-156T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695341 | ||||||
chr11:93695393
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1534-104G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695393 | ||||||
chr11:93695478
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1534-19A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695478 | ||||||
chr11:93695679
|
G | T | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.1671+45G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93695679 | ||||||
chr11:93695941
|
G | A | 2 | a0001c0001t0001g0128a0001c0016t0001g0009 | 3 | NA18956.hp1 NA19077.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1671+307G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93695941 | ||||||
chr11:93696069
|
G | A | 13 | a0003c0003t0001g0021a0003c0003t0001g0025a0003c0003t0001g0281others(10): Show | 15 | HG01081.hp1 HG01192.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1672-251G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93696069 | ||||||
chr11:93696162
|
A | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1672-158A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93696162 | ||||||
chr11:93700424
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5274+238T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700424 | ||||||
chr11:93700426
|
C | CT | 44 | a0001c0001t0001g0158a0001c0001t0001g0165a0001c0001t0001g0180others(41): Show | 50 | HG01074.hp2 HG01081.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.5274+257dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93700426 | |||||
chr11:93700426
|
CT | C | 13 | a0005c0006t0001g0274a0006c0004t0001g0002a0006c0004t0001g0027others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.5274+257delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93700426 | |||||
chr11:93700600
|
AT | A | 14 | a0005c0006t0001g0062a0006c0004t0001g0002a0006c0004t0001g0027others(11): Show | 17 | HG01099.hp1 HG02055.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.5274+427delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93700600 | |||||
chr11:93700731
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5274+545A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700731 | ||||||
chr11:93700755
|
T | A | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5274+569T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700755 | ||||||
chr11:93700757
|
T | C | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5274+571T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700757 | ||||||
chr11:93700758
|
T | C | 1 | a0027c0023t0001g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5274+572T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700758 | ||||||
chr11:93700765
|
T | G | 15 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(12): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5274+579T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700765 | ||||||
chr11:93700824
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5274+638T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700824 | ||||||
chr11:93700974
|
A | G | 2 | a0003c0010t0001g0022a0003c0010t0001g0292 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5274+788A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700974 | ||||||
chr11:93700990
|
C | CT | 15 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(12): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5274+804_5274+805i others(3): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700990 | ||||||
chr11:93701147
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.5274+961C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701147 | ||||||
chr11:93701278
|
T | A | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5274+1092T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701278 | ||||||
chr11:93701557
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5275-903T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701557 | ||||||
chr11:93701649
|
G | A | 15 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(12): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5275-811G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701649 | ||||||
chr11:93701717
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5275-743C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701717 | ||||||
chr11:93701879
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5275-581G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701879 | ||||||
chr11:93701935
|
GGTTGTTG others(8): Show |
G | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.5275-515_5275-501d others(17): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93701935 | |||||
chr11:93702108
|
A | G | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5275-352A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93702108 | ||||||
chr11:93702389
|
T | C | 1 | a0001c0012t0001g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5275-71T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93702389 | ||||||
chr11:93702747
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5453-29T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 16/29 | chr11 | 93702747 | ||||||
chr11:93703088
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.5596+169C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703088 | ||||||
chr11:93703109
|
G | A | 92 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(89): Show | 96 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.5596+190G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703109 | ||||||
chr11:93703166
|
A | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5596+247A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703166 | ||||||
chr11:93703177
|
C | T | 1 | a0001c0012t0001g0222 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5596+258C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703177 | ||||||
chr11:93703335
|
G | A | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5596+416G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703335 | ||||||
chr11:93703435
|
A | G | 1 | a0004c0005t0001g0101 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5596+516A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703435 | ||||||
chr11:93703477
|
T | C | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.5596+558T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703477 | ||||||
chr11:93703480
|
G | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.5596+561G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703480 | ||||||
chr11:93703544
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0129a0001c0001t0001g0137others(9): Show | 14 | HG00673.hp2 HG02074.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.5596+625T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703544 | ||||||
chr11:93703575
|
GT | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5596+668delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703575 | |||||
chr11:93703624
|
ACTGTT | A | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5596+713_5596+717d others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703624 | |||||
chr11:93703675
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5596+756G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703675 | ||||||
chr11:93703693
|
A | G | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5596+774A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703693 | ||||||
chr11:93703767
|
C | CT | 26 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(23): Show | 27 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.5596+867dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703767 | |||||
chr11:93703767
|
CT | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0258a0001c0001t0001g0262others(7): Show | 10 | HG01168.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.5596+867delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703767 | |||||
chr11:93703814
|
G | A | 2 | a0003c0010t0001g0022a0003c0010t0001g0292 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5596+895G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703814 | ||||||
chr11:93703825
|
G | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5596+906G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703825 | ||||||
chr11:93704008
|
A | T | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5596+1089A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704008 | ||||||
chr11:93704100
|
T | C | 2 | a0002c0002t0001g0092a0002c0002t0001g0109 | 2 | HG00673.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.5596+1181T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704100 | ||||||
chr11:93704134
|
C | G | 1 | a0003c0003t0001g0304 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5596+1215C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704134 | ||||||
chr11:93704253
|
A | C | 1 | a0002c0002t0001g0123 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5596+1334A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704253 | ||||||
chr11:93704398
|
G | A | 1 | a0031c0038t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5596+1479G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704398 | ||||||
chr11:93704405
|
C | G | 1 | a0005c0006t0001g0044 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5596+1486C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704405 | ||||||
chr11:93704411
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 6 | HG01192.hp2 HG01358.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.5596+1492C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704411 | ||||||
chr11:93704438
|
C | A | 31 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(28): Show | 37 | HG01081.hp1 HG01099.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.5596+1519C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704438 | ||||||
chr11:93704783
|
A | G | 3 | a0005c0011t0001g0246a0005c0011t0001g0248a0027c0023t0001g0247 | 3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.5596+1864A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704783 | ||||||
chr11:93704844
|
C | G | 97 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 101 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.5597-1901C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704844 | ||||||
chr11:93704984
|
C | T | 1 | a0015c0035t0001g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5597-1761C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704984 | ||||||
chr11:93705032
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5597-1713T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705032 | ||||||
chr11:93705039
|
T | C | 1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5597-1706T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705039 | ||||||
chr11:93705072
|
A | G | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5597-1673A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705072 | ||||||
chr11:93705194
|
C | T | 20 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(17): Show | 20 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.5597-1551C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705194 | ||||||
chr11:93705195
|
G | A | 15 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(12): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5597-1550G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705195 | ||||||
chr11:93705202
|
G | C | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5597-1543G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705202 | ||||||
chr11:93705289
|
C | CAAAGCAC others(10): Show |
1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5597-1452_5597-143 others(21): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93705289 | |||||
chr11:93705444
|
T | G | 5 | a0004c0005t0001g0086a0008c0008t0001g0083a0008c0008t0001g0084others(2): Show | 5 | HG02451.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.5597-1301T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705444 | ||||||
chr11:93705789
|
G | A | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5597-956G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705789 | ||||||
chr11:93705867
|
C | G | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5597-878C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705867 | ||||||
chr11:93706013
|
G | A | 1 | a0003c0010t0001g0022 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5597-732G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706013 | ||||||
chr11:93706069
|
G | A | 2 | a0011c0020t0001g0087a0011c0020t0001g0102 | 2 | HG02683.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.5597-676G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706069 | ||||||
chr11:93706080
|
G | T | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5597-665G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706080 | ||||||
chr11:93706166
|
G | A | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5597-579G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706166 | ||||||
chr11:93706256
|
C | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.5597-489C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706256 | ||||||
chr11:93706292
|
A | G | 1 | a0003c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5597-453A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706292 | ||||||
chr11:93706295
|
A | G | 1 | a0032c0041t0001g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5597-450A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706295 | ||||||
chr11:93706299
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0280a0003c0003t0001g0283others(1): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.5597-446A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706299 | ||||||
chr11:93706355
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0186a0001c0001t0001g0188others(1): Show | 5 | NA18971.hp1 NA18972.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.5597-390T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706355 | ||||||
chr11:93706394
|
T | C | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5597-351T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706394 | ||||||
chr11:93706636
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0130 | 3 | HG00741.hp1 HG01433.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.5597-109A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706636 | ||||||
chr11:93706727
|
A | T | 1 | a0003c0003t0001g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5597-18A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706727 | ||||||
chr11:93706735
|
T | C | 3 | a0002c0002t0001g0110a0005c0014t0001g0077a0005c0014t0001g0078 | 3 | HG02004.hp1 HG02280.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.5597-10T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706735 | ||||||
chr11:93707040
|
A | G | 2 | a0003c0019t0001g0288a0003c0019t0001g0289 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5749+143A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707040 | ||||||
chr11:93707099
|
C | CTTTTAAA others(11): Show |
3 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0176 | 3 | HG00140.hp2 HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.5749+202_5749+203i others(20): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707099 | ||||||
chr11:93707100
|
C | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0176 | 3 | HG00140.hp2 HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.5749+203C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707100 | ||||||
chr11:93707135
|
A | G | 55 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(52): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.5749+238A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707135 | ||||||
chr11:93707295
|
A | G | 2 | a0003c0010t0001g0022a0003c0010t0001g0292 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5749+398A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707295 | ||||||
chr11:93707441
|
A | G | 1 | a0018c0024t0001g0172 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5749+544A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707441 | ||||||
chr11:93707490
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5749+593G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707490 | ||||||
chr11:93707530
|
A | G | 3 | a0003c0003t0001g0024a0003c0003t0001g0296a0003c0003t0001g0297 | 4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5749+633A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707530 | ||||||
chr11:93707564
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+667C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707564 | ||||||
chr11:93707565
|
C | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+668C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707565 | ||||||
chr11:93707583
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5749+686A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707583 | ||||||
chr11:93707842
|
A | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+945A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707842 | ||||||
chr11:93707944
|
T | G | 1 | a0003c0003t0001g0305 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5749+1047T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707944 | ||||||
chr11:93707992
|
A | C | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+1095A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707992 | ||||||
chr11:93708084
|
T | C | 4 | a0002c0002t0001g0105a0002c0002t0001g0111a0002c0002t0001g0112others(1): Show | 4 | NA18949.hp1 NA19000.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.5749+1187T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708084 | ||||||
chr11:93708167
|
T | G | 1 | a0003c0003t0001g0301 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5749+1270T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708167 | ||||||
chr11:93708201
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5749+1304T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708201 | ||||||
chr11:93708206
|
A | G | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5749+1309A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708206 | ||||||
chr11:93708308
|
G | A | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+1411G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708308 | ||||||
chr11:93708512
|
C | G | 5 | a0007c0007t0001g0072a0007c0007t0001g0073a0007c0007t0001g0075others(2): Show | 5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5749+1615C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708512 | ||||||
chr11:93708521
|
T | TA | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+1625dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93708521 | |||||
chr11:93708526
|
G | A | 1 | a0003c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5749+1629G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708526 | ||||||
chr11:93708670
|
G | A | 6 | a0002c0002t0001g0093a0002c0002t0001g0094a0002c0002t0001g0095others(3): Show | 6 | HG02015.hp2 HG02148.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.5749+1773G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708670 | ||||||
chr11:93708684
|
G | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+1787G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708684 | ||||||
chr11:93708746
|
C | T | 300 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(297): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.5749+1849C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708746 | ||||||
chr11:93708767
|
C | T | 18 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(15): Show | 21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.5749+1870C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708767 | ||||||
chr11:93708913
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5749+2016C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708913 | ||||||
chr11:93709143
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0059 | 2 | HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.5749+2246A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709143 | ||||||
chr11:93709214
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.5749+2317C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709214 | ||||||
chr11:93709399
|
A | T | 1 | a0005c0006t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5749+2502A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709399 | ||||||
chr11:93709476
|
T | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.5749+2579T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709476 | ||||||
chr11:93709816
|
T | A | 3 | a0005c0011t0001g0246a0005c0011t0001g0248a0027c0023t0001g0247 | 3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.5749+2919T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709816 | ||||||
chr11:93709972
|
T | A | 3 | a0004c0009t0001g0037a0004c0009t0001g0038a0004c0009t0001g0124 | 3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5749+3075T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709972 | ||||||
chr11:93710062
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5749+3165T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710062 | ||||||
chr11:93710069
|
G | A | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+3172G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710069 | ||||||
chr11:93710133
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0126a0001c0001t0001g0135others(5): Show | 11 | HG00323.hp1 HG00609.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.5749+3236C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710133 | ||||||
chr11:93710134
|
G | A | 15 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(12): Show | 18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5749+3237G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710134 | ||||||
chr11:93710139
|
C | T | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+3242C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710139 | ||||||
chr11:93710209
|
A | AGGAT | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+3313_5749+331 others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93710209 | |||||
chr11:93710211
|
A | T | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+3314A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710211 | ||||||
chr11:93710225
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5749+3328G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710225 | ||||||
chr11:93710273
|
A | G | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+3376A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710273 | ||||||
chr11:93710372
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5749+3475A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710372 | ||||||
chr11:93710462
|
C | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(99): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.5749+3565C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710462 | ||||||
chr11:93710526
|
G | T | 1 | a0001c0001t0001g0264 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.5749+3629G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710526 | ||||||
chr11:93710616
|
A | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+3719A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710616 | ||||||
chr11:93710642
|
G | A | 1 | a0004c0043t0001g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5749+3745G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710642 | ||||||
chr11:93710711
|
G | A | 1 | a0004c0005t0001g0114 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5749+3814G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710711 | ||||||
chr11:93710730
|
G | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+3833G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710730 | ||||||
chr11:93710750
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5749+3853T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710750 | ||||||
chr11:93710891
|
T | C | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+3994T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710891 | ||||||
chr11:93710925
|
C | A | 4 | a0002c0002t0001g0088a0002c0002t0001g0089a0002c0002t0001g0096others(1): Show | 4 | NA18966.hp1 NA18979.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.5749+4028C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710925 | ||||||
chr11:93710986
|
CCTT | C | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+4093_5749+409 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93710986 | |||||
chr11:93711063
|
T | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5749+4166T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711063 | ||||||
chr11:93711213
|
T | C | 3 | a0003c0003t0001g0024a0003c0003t0001g0296a0003c0003t0001g0297 | 4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5749+4316T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711213 | ||||||
chr11:93711392
|
A | G | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG00408.hp2 NA18945.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5749+4495A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711392 | ||||||
chr11:93711481
|
G | GTTTTGT | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.5749+4618_5749+462 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711481 | |||||
chr11:93711481
|
GTTTTGT | G | 3 | a0001c0001t0001g0232a0009c0017t0002g0310a0009c0017t0002g0313 | 3 | HG01099.hp1 HG02056.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+4618_5749+462 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711481 | |||||
chr11:93711481
|
GTTTTGTT others(11): Show |
G | 1 | a0001c0001t0001g0226 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5749+4606_5749+462 others(22): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711481 | |||||
chr11:93711518
|
T | G | 1 | a0009c0017t0002g0310 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5749+4621T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711518 | ||||||
chr11:93711789
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5749+4892G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711789 | ||||||
chr11:93711826
|
GTT | G | 10 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0030others(7): Show | 13 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.5749+4941_5749+494 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711826 | |||||
chr11:93711829
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5749+4932T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711829 | ||||||
chr11:93711830
|
T | G | 4 | a0003c0010t0001g0022a0003c0010t0001g0292a0009c0017t0002g0310others(1): Show | 5 | HG01099.hp1 HG01884.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.5749+4933T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711830 | ||||||
chr11:93711834
|
T | G | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+4937T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711834 | ||||||
chr11:93712209
|
C | CT | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+5322dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712209 | |||||
chr11:93712209
|
CT | C | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+5322delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712209 | |||||
chr11:93712220
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+5323C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712220 | ||||||
chr11:93712261
|
T | A | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+5364T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712261 | ||||||
chr11:93712277
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5749+5380C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712277 | ||||||
chr11:93712289
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5749+5392C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712289 | ||||||
chr11:93712679
|
A | G | 1 | a0004c0005t0001g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5749+5782A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712679 | ||||||
chr11:93712832
|
T | C | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+5935T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712832 | ||||||
chr11:93712856
|
T | TTTG | 80 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(77): Show | 84 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.5749+5995_5749+599 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | |||||
chr11:93712856
|
T | TTTGTTG | 17 | a0001c0001t0001g0016a0001c0001t0001g0190a0001c0001t0001g0210others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.5749+5992_5749+599 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | |||||
chr11:93712856
|
T | TTTGTTGT others(2): Show |
5 | a0005c0006t0001g0042a0005c0011t0001g0246a0005c0011t0001g0248others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.5749+5989_5749+599 others(13): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | |||||
chr11:93712856
|
TTTG | T | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.5749+5995_5749+599 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | |||||
chr11:93712856
|
TTTGTTG | T | 15 | a0001c0001t0001g0057a0002c0002t0001g0095a0002c0002t0001g0113others(12): Show | 18 | HG02015.hp2 HG02165.hp1 HG02698.hp1 others(15): Show |
intron_variant | MODIFIER | c.5749+5992_5749+599 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | |||||
chr11:93712856
|
TTTGTTGT others(11): Show |
T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+5980_5749+599 others(22): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | |||||
chr11:93713211
|
CTGTT | C | 12 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(9): Show | 15 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(12): Show |
intron_variant | MODIFIER | c.5749+6316_5749+631 others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93713211 | |||||
chr11:93713228
|
G | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+6331G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713228 | ||||||
chr11:93713491
|
G | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+6594G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713491 | ||||||
chr11:93713492
|
C | T | 1 | a0002c0002t0001g0089 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.5749+6595C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713492 | ||||||
chr11:93713533
|
G | A | 1 | a0005c0006t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5749+6636G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713533 | ||||||
chr11:93713785
|
G | A | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+6888G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713785 | ||||||
chr11:93713914
|
A | ATTC | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+7019_5749+702 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93713914 | |||||
chr11:93713998
|
T | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+7101T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713998 | ||||||
chr11:93714022
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+7125C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714022 | ||||||
chr11:93714161
|
C | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.5750-7151C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714161 | ||||||
chr11:93714217
|
T | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0213 | 2 | NA18945.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.5750-7095T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714217 | ||||||
chr11:93714247
|
G | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5750-7065G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714247 | ||||||
chr11:93714275
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.5750-7037G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714275 | ||||||
chr11:93714291
|
T | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-7021T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714291 | ||||||
chr11:93714376
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5750-6936A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714376 | ||||||
chr11:93714395
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(53): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5750-6917C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714395 | ||||||
chr11:93714407
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-6905C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714407 | ||||||
chr11:93714570
|
G | A | 1 | a0005c0033t0001g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5750-6742G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714570 | ||||||
chr11:93714660
|
T | G | 2 | a0003c0019t0001g0288a0003c0019t0001g0289 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5750-6652T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714660 | ||||||
chr11:93714673
|
C | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-6639C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714673 | ||||||
chr11:93714788
|
G | A | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5750-6524G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714788 | ||||||
chr11:93714790
|
A | T | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-6522A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714790 | ||||||
chr11:93714810
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.5750-6502T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714810 | ||||||
chr11:93714827
|
A | G | 1 | a0006c0004t0001g0033 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.5750-6485A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714827 | ||||||
chr11:93714842
|
C | CCT | 67 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0079others(64): Show | 79 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.5750-6451_5750-645 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93714842 | |||||
chr11:93715097
|
C | T | 1 | a0009c0017t0002g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5750-6215C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715097 | ||||||
chr11:93715140
|
C | T | 1 | a0005c0006t0001g0276 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5750-6172C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715140 | ||||||
chr11:93715193
|
A | G | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-6119A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715193 | ||||||
chr11:93715302
|
TG | T | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-6009delG | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715302 | ||||||
chr11:93715353
|
G | T | 1 | a0006c0004t0001g0035 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5750-5959G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715353 | ||||||
chr11:93715423
|
A | G | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.5750-5889A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715423 | ||||||
chr11:93715591
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5750-5721G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715591 | ||||||
chr11:93715654
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.5750-5658T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715654 | ||||||
chr11:93715732
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5750-5580A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715732 | ||||||
chr11:93715760
|
T | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-5552T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715760 | ||||||
chr11:93715843
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5750-5469A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715843 | ||||||
chr11:93715896
|
G | A | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-5416G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715896 | ||||||
chr11:93716013
|
C | T | 1 | a0001c0001t0001g0019 | 2 | NA18966.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.5750-5299C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716013 | ||||||
chr11:93716021
|
G | A | 1 | a0003c0003t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5750-5291G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716021 | ||||||
chr11:93716187
|
A | G | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-5125A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716187 | ||||||
chr11:93716233
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-5079C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716233 | ||||||
chr11:93716287
|
A | C | 12 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0054others(9): Show | 12 | HG00140.hp2 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.5750-5025A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716287 | ||||||
chr11:93716457
|
C | T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-4855C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716457 | ||||||
chr11:93716471
|
G | A | 1 | a0005c0006t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5750-4841G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716471 | ||||||
chr11:93716531
|
T | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-4781T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716531 | ||||||
chr11:93716549
|
G | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5750-4763G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716549 | ||||||
chr11:93716569
|
C | T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-4743C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716569 | ||||||
chr11:93716606
|
C | T | 3 | a0004c0009t0001g0037a0004c0009t0001g0038a0004c0009t0001g0124 | 3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5750-4706C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716606 | ||||||
chr11:93716652
|
G | T | 8 | a0003c0003t0001g0021a0003c0003t0001g0025a0003c0003t0001g0281others(5): Show | 10 | HG01081.hp1 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.5750-4660G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716652 | ||||||
chr11:93716968
|
A | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.5750-4344A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716968 | ||||||
chr11:93717004
|
C | T | 2 | a0005c0006t0001g0042a0024c0028t0001g0041 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5750-4308C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717004 | ||||||
chr11:93717043
|
A | C | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-4269A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717043 | ||||||
chr11:93717132
|
C | T | 2 | a0005c0006t0001g0274a0005c0006t0001g0275 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5750-4180C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717132 | ||||||
chr11:93717162
|
A | C | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-4150A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717162 | ||||||
chr11:93717168
|
C | T | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-4144C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717168 | ||||||
chr11:93717212
|
G | T | 1 | a0031c0038t0001g0279 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5750-4100G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717212 | ||||||
chr11:93717386
|
G | A | 1 | a0005c0006t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5750-3926G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717386 | ||||||
chr11:93717751
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5750-3561T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717751 | ||||||
chr11:93717780
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3532C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717780 | ||||||
chr11:93717904
|
G | A | 6 | a0001c0001t0001g0220a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG02622.hp1 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5750-3408G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717904 | ||||||
chr11:93717911
|
A | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3401A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717911 | ||||||
chr11:93718036
|
C | T | 1 | a0003c0010t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5750-3276C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718036 | ||||||
chr11:93718040
|
T | G | 4 | a0008c0008t0001g0083a0008c0008t0001g0084a0008c0008t0001g0085others(1): Show | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5750-3272T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718040 | ||||||
chr11:93718092
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5750-3220G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718092 | ||||||
chr11:93718128
|
C | A | 1 | a0001c0001t0001g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5750-3184C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718128 | ||||||
chr11:93718172
|
A | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3140A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718172 | ||||||
chr11:93718181
|
G | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-3131G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718181 | ||||||
chr11:93718198
|
A | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3114A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718198 | ||||||
chr11:93718249
|
A | G | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5750-3063A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718249 | ||||||
chr11:93718392
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5750-2920G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718392 | ||||||
chr11:93718465
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 11 | HG01109.hp2 HG01192.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.5750-2847T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718465 | ||||||
chr11:93718570
|
C | T | 1 | a0002c0002t0001g0079 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5750-2742C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718570 | ||||||
chr11:93719105
|
C | CA | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.5750-2199dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93719105 | |||||
chr11:93719221
|
T | A | 265 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(262): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.5750-2091T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719221 | ||||||
chr11:93719246
|
G | GGT | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-2066_5750-206 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719246 | ||||||
chr11:93719246
|
G | GT | 37 | a0001c0001t0001g0179a0002c0002t0001g0109a0002c0002t0001g0120others(34): Show | 43 | HG00673.hp1 HG01074.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.5750-2052dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93719246 | |||||
chr11:93719246
|
GT | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(97): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.5750-2052delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93719246 | |||||
chr11:93719247
|
T | G | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5750-2065T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719247 | ||||||
chr11:93719349
|
A | G | 1 | a0009c0017t0002g0310 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5750-1963A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719349 | ||||||
chr11:93719465
|
G | C | 2 | a0001c0013t0001g0206a0001c0013t0001g0209 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.5750-1847G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719465 | ||||||
chr11:93719605
|
C | G | 1 | a0001c0001t0001g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5750-1707C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719605 | ||||||
chr11:93719626
|
A | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-1686A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719626 | ||||||
chr11:93719702
|
T | G | 1 | a0003c0003t0001g0282 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5750-1610T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719702 | ||||||
chr11:93719928
|
A | C | 261 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(258): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.5750-1384A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719928 | ||||||
chr11:93720062
|
T | TA | 296 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(293): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.5750-1236dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720062 | |||||
chr11:93720062
|
TA | T | 13 | a0005c0033t0001g0039a0006c0004t0001g0002a0006c0004t0001g0027others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03041.hp2 others(13): Show |
intron_variant | MODIFIER | c.5750-1236delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720062 | |||||
chr11:93720083
|
C | T | 3 | a0005c0011t0001g0246a0005c0011t0001g0248a0027c0023t0001g0247 | 3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.5750-1229C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720083 | ||||||
chr11:93720114
|
TCAGGAGG others(6): Show |
T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-1190_5750-117 others(17): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720114 | |||||
chr11:93720270
|
C | T | 89 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(86): Show | 93 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.5750-1042C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720270 | ||||||
chr11:93720271
|
G | A | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5750-1041G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720271 | ||||||
chr11:93720289
|
A | G | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-1023A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720289 | ||||||
chr11:93720308
|
A | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-1004A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720308 | ||||||
chr11:93720381
|
G | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-931G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720381 | ||||||
chr11:93720450
|
G | A | 1 | a0006c0004t0001g0029 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.5750-862G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720450 | ||||||
chr11:93720473
|
CA | C | 17 | a0003c0003t0001g0020a0003c0003t0001g0021a0003c0003t0001g0025others(14): Show | 20 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.5750-822delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720473 | |||||
chr11:93720489
|
A | AAAAAAAG | 16 | a0001c0001t0001g0006a0001c0001t0001g0129a0001c0001t0001g0137others(13): Show | 18 | HG00673.hp2 HG02055.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(9): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | |||||
chr11:93720489
|
A | AAAAAAG | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(90): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | |||||
chr11:93720489
|
A | AAAAAG | 155 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(152): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | |||||
chr11:93720489
|
A | AAAAG | 6 | a0001c0001t0001g0203a0005c0014t0001g0077a0005c0014t0001g0078others(3): Show | 6 | HG02004.hp1 HG02280.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | |||||
chr11:93720489
|
A | AAAG | 10 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(7): Show | 13 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(5): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | |||||
chr11:93720589
|
T | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-723T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720589 | ||||||
chr11:93720616
|
G | A | 1 | a0005c0014t0001g0078 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5750-696G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720616 | ||||||
chr11:93720785
|
T | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-527T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720785 | ||||||
chr11:93720922
|
T | C | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5750-390T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720922 | ||||||
chr11:93720926
|
TGCATGTT others(3): Show |
T | 1 | a0003c0003t0001g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5750-381_5750-372d others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720926 | |||||
chr11:93720981
|
T | A | 1 | a0002c0002t0001g0093 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5750-331T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720981 | ||||||
chr11:93721453
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5850+41T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721453 | ||||||
chr11:93721477
|
A | G | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5850+65A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721477 | ||||||
chr11:93721491
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5850+79A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721491 | ||||||
chr11:93721665
|
G | GGT | 82 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 89 | HG00323.hp2 HG00621.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.5851-254_5851-253d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | |||||
chr11:93721665
|
G | GGTGT | 12 | a0001c0001t0001g0069a0001c0001t0001g0180a0001c0001t0001g0185others(9): Show | 12 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.5851-256_5851-253d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | |||||
chr11:93721665
|
G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0213others(1): Show | 4 | HG00408.hp2 HG02004.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.5851-260_5851-253d others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | |||||
chr11:93721665
|
GGT | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0057a0001c0001t0001g0126others(69): Show | 84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.5851-254_5851-253d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | |||||
chr11:93721665
|
GGTGT | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(110): Show | 131 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.5851-256_5851-253d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | |||||
chr11:93721665
|
GGTGTGT | G | 8 | a0001c0001t0001g0143a0001c0001t0001g0160a0001c0001t0001g0262others(5): Show | 8 | HG00438.hp1 HG02080.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.5851-258_5851-253d others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | |||||
chr11:93721665
|
GGTGTGTG others(3): Show |
G | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5851-262_5851-253d others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | |||||
chr11:93721722
|
A | AT | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5851-231dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721722 | |||||
chr11:93721726
|
C | G | 1 | a0003c0010t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5851-228C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721726 | ||||||
chr11:93722089
|
C | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0173a0001c0001t0001g0175others(2): Show | 5 | HG01358.hp2 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.5947+39C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722089 | ||||||
chr11:93722248
|
C | G | 3 | a0003c0003t0001g0024a0003c0003t0001g0296a0003c0003t0001g0297 | 4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5947+198C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722248 | ||||||
chr11:93722277
|
G | A | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.5947+227G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722277 | ||||||
chr11:93722355
|
A | G | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5947+305A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722355 | ||||||
chr11:93722395
|
A | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0217 | 2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.5947+345A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722395 | ||||||
chr11:93722418
|
C | T | 3 | a0005c0006t0001g0274a0005c0006t0001g0275a0005c0006t0001g0276 | 3 | HG02895.hp2 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5947+368C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722418 | ||||||
chr11:93722505
|
C | T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5947+455C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722505 | ||||||
chr11:93722826
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 6 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.5948-215C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722826 | ||||||
chr11:93722854
|
G | A | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5948-187G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722854 | ||||||
chr11:93722924
|
G | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5948-117G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722924 | ||||||
chr11:93723031
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5948-10C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93723031 | ||||||
chr11:93723385
|
A | G | 1 | a0005c0006t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6196+96A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723385 | ||||||
chr11:93723549
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.6196+260G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723549 | ||||||
chr11:93723589
|
C | G | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(103): Show | 121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.6196+300C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723589 | ||||||
chr11:93723606
|
C | T | 2 | a0002c0002t0001g0005a0014c0044t0001g0081 | 4 | NA18747.hp1 NA18945.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.6196+317C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723606 | ||||||
chr11:93723910
|
C | T | 1 | a0004c0005t0001g0114 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6197-344C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723910 | ||||||
chr11:93723969
|
A | T | 14 | a0003c0003t0001g0287a0006c0004t0001g0002a0006c0004t0001g0027others(11): Show | 17 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(14): Show |
intron_variant | MODIFIER | c.6197-285A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723969 | ||||||
chr11:93723970
|
T | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0204 | 2 | HG02738.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.6197-284T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723970 | ||||||
chr11:93724150
|
G | A | 2 | a0001c0001t0001g0164a0033c0042t0001g0154 | 2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.6197-104G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724150 | ||||||
chr11:93724150
|
G | T | 1 | a0002c0002t0001g0097 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.6197-104G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724150 | ||||||
chr11:93724163
|
T | C | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6197-91T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724163 | ||||||
chr11:93724239
|
A | T | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6197-15A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724239 | ||||||
chr11:93724536
|
G | A | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.6318+161G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724536 | ||||||
chr11:93724598
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6318+223C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724598 | ||||||
chr11:93724638
|
G | A | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.6318+263G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724638 | ||||||
chr11:93724665
|
G | T | 1 | a0001c0016t0001g0009 | 2 | NA19077.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.6318+290G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724665 | ||||||
chr11:93724702
|
G | A | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.6318+327G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724702 | ||||||
chr11:93724722
|
G | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6318+347G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724722 | ||||||
chr11:93724853
|
A | C | 4 | a0003c0003t0001g0020a0003c0003t0001g0280a0003c0003t0001g0283others(1): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6318+478A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724853 | ||||||
chr11:93724876
|
T | C | 1 | a0004c0005t0001g0101 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6318+501T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724876 | ||||||
chr11:93724886
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6318+511T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724886 | ||||||
chr11:93724970
|
T | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.6318+595T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724970 | ||||||
chr11:93724992
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.6318+617T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724992 | ||||||
chr11:93725026
|
A | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.6319-625A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725026 | ||||||
chr11:93725114
|
G | C | 1 | a0005c0006t0001g0043 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6319-537G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725114 | ||||||
chr11:93725147
|
G | A | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.6319-504G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725147 | ||||||
chr11:93725201
|
C | T | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(256): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6319-450C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725201 | ||||||
chr11:93725587
|
G | A | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6319-64G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725587 | ||||||
chr11:93725612
|
T | C | 1 | a0003c0010t0001g0022 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6319-39T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725612 | ||||||
chr11:93725865
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6499+34T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93725865 | ||||||
chr11:93726053
|
TTCCCTAC others(7): Show |
T | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6499+223_6499+236d others(16): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726053 | ||||||
chr11:93726071
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6499+240A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726071 | ||||||
chr11:93726097
|
A | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.6499+266A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726097 | ||||||
chr11:93726225
|
G | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6499+394G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726225 | ||||||
chr11:93726342
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6499+511C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726342 | ||||||
chr11:93726361
|
C | G | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(259): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.6499+530C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726361 | ||||||
chr11:93726472
|
C | T | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6500-504C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726472 | ||||||
chr11:93726738
|
TATAGCCA others(25): Show |
T | 1 | a0029c0039t0001g0307 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6500-236_6500-205d others(34): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr11 | 93726738 | |||||
chr11:93727695
|
T | C | 4 | a0003c0003t0001g0025a0003c0003t0001g0308a0003c0003t0001g0309others(1): Show | 5 | NA18953.hp1 NA18968.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.7161+58T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727695 | ||||||
chr11:93727728
|
A | G | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.7161+91A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727728 | ||||||
chr11:93727731
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7161+94C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727731 | ||||||
chr11:93727770
|
C | T | 1 | a0022c0030t0001g0215 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7161+133C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727770 | ||||||
chr11:93727895
|
A | G | 6 | a0005c0006t0001g0040a0005c0006t0001g0042a0005c0006t0001g0274others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.7161+258A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727895 | ||||||
chr11:93728015
|
T | A | 2 | a0010c0018t0001g0311a0010c0018t0001g0312 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.7161+378T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728015 | ||||||
chr11:93728056
|
A | G | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7161+419A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728056 | ||||||
chr11:93728196
|
A | C | 1 | a0001c0001t0001g0277 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.7162-485A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728196 | ||||||
chr11:93728235
|
G | A | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(259): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7162-446G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728235 | ||||||
chr11:93728274
|
C | G | 1 | a0004c0005t0001g0104 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7162-407C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728274 | ||||||
chr11:93728329
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7162-352C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728329 | ||||||
chr11:93728434
|
C | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0252 | 2 | HG00621.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.7162-247C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728434 | ||||||
chr11:93728555
|
T | C | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.7162-126T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728555 | ||||||
chr11:93728674
|
T | G | 1 | a0029c0039t0001g0307 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-7T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728674 | ||||||
chr11:93728675
|
T | G | 1 | a0029c0039t0001g0307 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-6T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728675 | ||||||
chr11:93728676
|
C | G | 1 | a0029c0039t0001g0307 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-5C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728676 | ||||||
chr11:93728677
|
A | G | 1 | a0029c0039t0001g0307 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-4A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728677 | ||||||
chr11:93728678
|
C | G | 1 | a0029c0039t0001g0307 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-3C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728678 | ||||||
chr11:93728679
|
A | G | 1 | a0029c0039t0001g0307 | 1 | NA18986.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.7162-2A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728679 | ||||||
chr11:93728891
|
T | G | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7302+70T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93728891 | ||||||
chr11:93728936
|
G | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.7302+115G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93728936 | ||||||
chr11:93729039
|
G | C | 2 | a0005c0014t0001g0077a0005c0014t0001g0078 | 2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.7302+218G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729039 | ||||||
chr11:93729159
|
A | G | 1 | a0009c0017t0002g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7303-275A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729159 | ||||||
chr11:93729359
|
C | T | 1 | a0005c0006t0001g0276 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7303-75C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729359 | ||||||
chr11:93729385
|
C | T | 2 | a0009c0017t0002g0310a0009c0017t0002g0313 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7303-49C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729385 | ||||||
chr11:93729394
|
C | T | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7303-40C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729394 | ||||||
chr11:93729403
|
A | AGAGTT | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7303-27_7303-26ins others(5): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr11 | 93729403 | |||||
chr11:93729414
|
T | C | 1 | a0003c0010t0001g0022 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.7303-20T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729414 | ||||||
chr11:93729415
|
G | C | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7303-19G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729415 | ||||||
chr11:93729419
|
C | CT | 11 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(8): Show | 14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.7303-12dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr11 | 93729419 | |||||
chr11:93729553
|
A | T | 1 | a0005c0026t0001g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7399+23A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/29 | chr11 | 93729553 | ||||||
chr11:93729603
|
T | TC | 13 | a0006c0004t0001g0002a0006c0004t0001g0027a0006c0004t0001g0029others(10): Show | 16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.7400-6dupC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr11 | 93729603 | |||||
chr11:93729975
|
GTTAA | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7667+9_7667+12delA others(3): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr11 | 93729975 | |||||
chr11:93729979
|
A | AT | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 129 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.7667+26dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr11 | 93729979 | |||||
chr11:93730151
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G | A | 1 | a0005c0006t0001g0062 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.7767+3G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 29/29 | chr11 | 93730151 | ||||||
chr11:93730166
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A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(277): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.7767+18A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 29/29 | chr11 | 93730166 | ||||||
chr11:93730221
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C | T | 1 | a0005c0006t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7768-10C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 29/29 | chr11 | 93730221 |