geneid | 80321 |
---|---|
ensemblid | ENSG00000114107.9 |
hgncid | 29972 |
symbol | CEP70 |
name | centrosomal protein 70 |
refseq_nuc | NM_024491.4 |
refseq_prot | NP_077817.2 |
ensembl_nuc | ENST00000264982.8 |
ensembl_prot | ENSP00000264982.3 |
mane_status | MANE Select |
chr | chr3 |
start | 138494344 |
end | 138594260 |
strand | - |
ver | v1.2 |
region | chr3:138494344-138594260 |
region5000 | chr3:138489344-138599260 |
regionname0 | CEP70_chr3_138494344_138594260 |
regionname5000 | CEP70_chr3_138489344_138599260 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 597 | 118 | 16 | 23 | 59 | 5 | 15 | 44 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0002 | 0/1 | 597 | 105 | 34 | 6 | 54 | 0 | 10 | 40 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003 | 1/0 | 597 | 89 | 31 | 19 | 13 | 9 | 16 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0004 | 0/0 | 597 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0005 | 0/0 | 597 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0006 | 0/0 | 597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0007 | 0/0 | 597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1794 | 111 | 9 | 23 | 59 | 5 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0002 | 0/1 | 1794 | 104 | 34 | 6 | 53 | 0 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0003 | 0/0 | 1794 | 81 | 25 | 19 | 13 | 8 | 16 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0004 | 0/0 | 1794 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0005 | 0/0 | 1794 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0006 | 0/0 | 1794 | 3 | 2 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0007 | 1/0 | 1794 | 2 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0008 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0009 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0010 | 0/0 | 1794 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0011 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
c0012 | 0/0 | 1794 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 843 | 145 | 31 | 31 | 59 | 7 | 17 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
t0002 | 0/1 | 843 | 82 | 14 | 3 | 54 | 0 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
t0003 | 0/0 | 838 | 79 | 30 | 14 | 13 | 7 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
t0004 | 1/0 | 843 | 7 | 5 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
t0005 | 0/0 | 843 | 3 | 2 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
t0006 | 0/0 | 843 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0022 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1794 | 111 | 9 | 23 | 59 | 5 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0001c0004 | 0/0 | 1794 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0001c0011 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0002c0002 | 0/1 | 1794 | 104 | 34 | 6 | 53 | 0 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0002c0012 | 0/0 | 1794 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0003 | 0/0 | 1794 | 81 | 25 | 19 | 13 | 8 | 16 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0005 | 0/0 | 1794 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0007 | 1/0 | 1794 | 2 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0004c0006 | 0/0 | 1794 | 3 | 2 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0005c0008 | 0/0 | 1794 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0006c0010 | 0/0 | 1794 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0007c0009 | 0/0 | 1794 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2636 | 111 | 9 | 23 | 59 | 5 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0001c0004t0004 | 0/0 | 2636 | 4 | 4 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0001c0004t0006 | 0/0 | 2636 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0001c0011t0001 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0002c0002t0001 | 0/0 | 2636 | 23 | 20 | 3 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0002c0002t0002 | 0/1 | 2636 | 81 | 14 | 3 | 53 | 0 | 10 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0002c0012t0002 | 0/0 | 2636 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0003t0001 | 0/0 | 2636 | 9 | 1 | 5 | 0 | 2 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0003t0003 | 0/0 | 2631 | 72 | 24 | 14 | 13 | 6 | 15 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0005t0003 | 0/0 | 2631 | 6 | 6 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0007t0003 | 0/0 | 2631 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0003c0007t0004 | 1/0 | 2636 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0004c0006t0005 | 0/0 | 2636 | 3 | 2 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0005c0008t0001 | 0/0 | 2636 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0006c0010t0004 | 0/0 | 2636 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
a0007c0009t0004 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | copy fasta | chr3 | 138489344 | 138599260 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0004t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0004t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0004t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0004t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0004t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0004t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0001c0011t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0022 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0002c0012t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0005t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0005t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0005t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0005t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0005t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0005t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0007t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0003c0007t0004g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0004c0006t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0004c0006t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0004c0006t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0005c0008t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0006c0010t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
a0007c0009t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0003 | t0003 | g0063 | EUR | GBR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00280 | hp2 | a0003 | c0003 | t0003 | g0070 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00323 | hp1 | a0003 | c0007 | t0003 | g0045 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00323 | hp2 | a0003 | c0003 | t0003 | g0071 | EUR | FIN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00621 | hp1 | a0003 | c0003 | t0003 | g0047 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0073 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00673 | hp2 | a0003 | c0003 | t0003 | g0048 | EAS | CHS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00735 | hp1 | a0003 | c0003 | t0003 | g0093 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00735 | hp2 | a0004 | c0006 | t0005 | g0030 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01069 | hp1 | a0003 | c0003 | t0003 | g0069 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0067 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01099 | hp2 | a0003 | c0003 | t0003 | g0055 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01106 | hp2 | a0003 | c0003 | t0003 | g0044 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01109 | hp2 | a0003 | c0003 | t0003 | g0091 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01167 | hp1 | a0003 | c0003 | t0003 | g0102 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01168 | hp1 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01169 | hp1 | a0003 | c0003 | t0003 | g0104 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01175 | hp1 | a0003 | c0003 | t0003 | g0011 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01243 | hp1 | a0006 | c0010 | t0004 | g0023 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01243 | hp2 | a0003 | c0003 | t0003 | g0098 | AMR | PUR | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01256 | hp1 | a0003 | c0003 | t0003 | g0092 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01257 | hp2 | a0003 | c0003 | t0001 | g0072 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01258 | hp1 | a0003 | c0003 | t0001 | g0075 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0240 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01433 | hp2 | a0003 | c0003 | t0003 | g0010 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01496 | hp1 | a0003 | c0003 | t0003 | g0039 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0202 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01516 | hp1 | a0003 | c0003 | t0001 | g0074 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01516 | hp2 | a0003 | c0003 | t0003 | g0053 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01517 | hp1 | a0003 | c0003 | t0003 | g0052 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0221 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01891 | hp1 | a0004 | c0006 | t0005 | g0031 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02004 | hp1 | a0003 | c0003 | t0003 | g0085 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0219 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02080 | hp1 | a0003 | c0003 | t0003 | g0043 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | KHV | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02145 | hp1 | a0003 | c0003 | t0003 | g0068 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02148 | hp1 | a0003 | c0003 | t0003 | g0061 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | CDX | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02258 | hp1 | a0001 | c0004 | t0004 | g0109 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02280 | hp1 | a0003 | c0005 | t0003 | g0088 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0220 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02451 | hp2 | a0003 | c0005 | t0003 | g0078 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02572 | hp1 | a0003 | c0003 | t0003 | g0108 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02602 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02615 | hp2 | a0001 | c0004 | t0006 | g0029 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02622 | hp1 | a0003 | c0003 | t0003 | g0101 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02622 | hp2 | a0003 | c0003 | t0003 | g0213 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02630 | hp2 | a0003 | c0003 | t0003 | g0003 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02647 | hp1 | a0003 | c0003 | t0003 | g0106 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02683 | hp1 | a0003 | c0003 | t0003 | g0054 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0245 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02723 | hp2 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02738 | hp1 | a0003 | c0003 | t0001 | g0060 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02818 | hp1 | a0003 | c0003 | t0003 | g0059 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02818 | hp2 | a0003 | c0003 | t0003 | g0095 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02895 | hp2 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02897 | hp1 | a0003 | c0003 | t0003 | g0103 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02897 | hp2 | a0003 | c0003 | t0003 | g0094 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02922 | hp1 | a0003 | c0005 | t0003 | g0058 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02965 | hp1 | a0003 | c0003 | t0003 | g0097 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02970 | hp1 | a0003 | c0003 | t0003 | g0057 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03041 | hp2 | a0001 | c0004 | t0004 | g0110 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03098 | hp1 | a0003 | c0003 | t0003 | g0076 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03098 | hp2 | a0003 | c0003 | t0003 | g0056 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03130 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03139 | hp2 | a0001 | c0011 | t0001 | g0111 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03195 | hp2 | a0001 | c0004 | t0004 | g0215 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03225 | hp1 | a0003 | c0003 | t0003 | g0107 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03225 | hp2 | a0007 | c0009 | t0004 | g0217 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03239 | hp2 | a0003 | c0003 | t0003 | g0009 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03453 | hp1 | a0001 | c0004 | t0006 | g0032 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03453 | hp2 | a0003 | c0003 | t0003 | g0003 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0100 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03490 | hp1 | a0003 | c0003 | t0003 | g0009 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03516 | hp2 | a0001 | c0004 | t0004 | g0216 | AFR | ESN | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03579 | hp1 | a0003 | c0003 | t0003 | g0105 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0261 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03669 | hp1 | a0003 | c0003 | t0003 | g0084 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03688 | hp1 | a0003 | c0003 | t0003 | g0062 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0022 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03704 | hp2 | a0003 | c0003 | t0003 | g0041 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0087 | SAS | PJL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03831 | hp1 | a0003 | c0003 | t0003 | g0066 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0020 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03834 | hp1 | a0003 | c0003 | t0003 | g0046 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0234 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03927 | hp1 | a0003 | c0003 | t0003 | g0214 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0265 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03942 | hp2 | a0003 | c0003 | t0003 | g0064 | SAS | BEB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG04115 | hp1 | a0003 | c0003 | t0003 | g0090 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG04199 | hp1 | a0003 | c0003 | t0003 | g0065 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | CHB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18939 | hp2 | a0003 | c0003 | t0003 | g0042 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18941 | hp1 | a0002 | c0012 | t0002 | g0268 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18957 | hp2 | a0003 | c0003 | t0003 | g0114 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18968 | hp2 | a0003 | c0003 | t0003 | g0034 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18980 | hp2 | a0003 | c0003 | t0003 | g0113 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18986 | hp2 | a0003 | c0003 | t0003 | g0050 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19002 | hp1 | a0003 | c0003 | t0003 | g0115 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19082 | hp2 | a0003 | c0003 | t0003 | g0081 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19086 | hp2 | a0003 | c0003 | t0003 | g0082 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19087 | hp2 | a0003 | c0003 | t0003 | g0083 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0260 | AFR | YRI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA19240 | hp2 | a0003 | c0003 | t0003 | g0077 | AFR | YRI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20129 | hp1 | a0003 | c0005 | t0003 | g0079 | AFR | ASW | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | ASW | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20752 | hp2 | a0003 | c0003 | t0003 | g0049 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20805 | hp2 | a0003 | c0003 | t0001 | g0192 | EUR | TSI | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20905 | hp1 | a0003 | c0003 | t0003 | g0096 | SAS | GIH | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA20905 | hp2 | a0005 | c0008 | t0001 | g0190 | SAS | GIH | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | CLM | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02559 | hp1 | a0003 | c0003 | t0003 | g0099 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG02559 | hp2 | a0003 | c0005 | t0003 | g0089 | AFR | ACB | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG03471 | hp2 | a0003 | c0005 | t0003 | g0080 | AFR | MSL | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | USA | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
HG06807 | hp2 | a0004 | c0006 | t0005 | g0028 | AFR | USA | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
NA21309 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | LWK | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0022 | REF | REF | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
homoSapiens_grch38 | hp1 | a0003 | c0007 | t0004 | g0051 | REF | REF | CEP70_chr3_138489344_138599260 | CEP70 | chr3 | 138489344 | 138599260 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138500152
|
T | C | 1 | a0002 | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
missense_variant | MODERATE | c.1610A>G | p.Asn537Ser | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/18 | 1781/2636 | 1610/1794 | 537/597 | chr3 | 138500152 | ||
chr3:138500549
|
A | G | 1 | a0006 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1387T>C | p.Phe463Leu | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 15/18 | 1558/2636 | 1387/1794 | 463/597 | chr3 | 138500549 | ||
chr3:138500832
|
A | T | 1 | a0004 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.1271T>A | p.Leu424His | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/18 | 1442/2636 | 1271/1794 | 424/597 | chr3 | 138500832 | ||
chr3:138505372
|
C | T | 1 | a0007 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1144G>A | p.Asp382Asn | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/18 | 1315/2636 | 1144/1794 | 382/597 | chr3 | 138505372 | ||
chr3:138570379
|
C | T | 6 | a0001a0002a0004others(3): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
missense_variant | MODERATE | c.404G>A | p.Ser135Asn | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/18 | 575/2636 | 404/1794 | 135/597 | chr3 | 138570379 | ||
chr3:138570472
|
C | T | 1 | a0005 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.311G>A | p.Arg104Gln | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/18 | 482/2636 | 311/1794 | 104/597 | chr3 | 138570472 | ||
chr3:138572893
|
C | T | 1 | a0004 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.35G>A | p.Ser12Asn | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/18 | 206/2636 | 35/1794 | 12/597 | chr3 | 138572893 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138500827
|
A | G | 1 | a0001c0011 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1276T>C | p.Leu426Leu | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/18 | 1447/2636 | 1276/1794 | 426/597 | chr3 | 138500827 | ||
chr3:138525558
|
C | T | 3 | a0003c0003a0003c0005a0004c0006 | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
synonymous_variant | LOW | c.876G>A | p.Thr292Thr | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/18 | 1047/2636 | 876/1794 | 292/597 | chr3 | 138525558 | ||
chr3:138570321
|
T | C | 5 | a0001c0001a0001c0011a0002c0012others(2): Show | 120 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(117): Show |
synonymous_variant | LOW | c.462A>G | p.Leu154Leu | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/18 | 633/2636 | 462/1794 | 154/597 | chr3 | 138570321 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138494450
|
C | T | 2 | a0002c0002t0002a0002c0012t0002 | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*565G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 18/18 | 565 | chr3 | 138494450 | |||||
chr3:138494867
|
T | C | 6 | a0001c0001t0001a0001c0004t0006a0001c0011t0001others(3): Show | 147 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*148A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 18/18 | 148 | chr3 | 138494867 | |||||
chr3:138495007
|
ATTTGT | A | 3 | a0003c0003t0003a0003c0005t0003a0003c0007t0003 | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3_*7delACAAA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 18/18 | 3 | chr3 | 138495007 | |||||
chr3:138591865
|
C | T | 2 | a0001c0004t0006a0004c0006t0005 | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-17G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/18 | 18938 | chr3 | 138591865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:138495552
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1733-476T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495552 | ||||||
chr3:138495652
|
G | C | 67 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(64): Show | 79 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1733-576C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495652 | ||||||
chr3:138495669
|
C | T | 1 | a0003c0003t0003g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1733-593G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495669 | ||||||
chr3:138495790
|
T | G | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1733-714A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495790 | ||||||
chr3:138495862
|
C | A | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1733-786G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495862 | ||||||
chr3:138495984
|
C | A | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1733-908G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138495984 | ||||||
chr3:138496196
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1733-1120C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496196 | ||||||
chr3:138496203
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1733-1127G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496203 | ||||||
chr3:138496272
|
C | T | 152 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(149): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1733-1196G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496272 | ||||||
chr3:138496318
|
CT | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1733-1243delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496318 | ||||||
chr3:138496351
|
T | C | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1733-1275A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496351 | ||||||
chr3:138496445
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1733-1369C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496445 | ||||||
chr3:138496535
|
A | T | 1 | a0001c0004t0006g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1733-1459T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496535 | ||||||
chr3:138496618
|
G | A | 1 | a0002c0002t0002g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1732+1413C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496618 | ||||||
chr3:138496673
|
C | A | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1732+1358G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496673 | ||||||
chr3:138496703
|
A | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1732+1328T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496703 | ||||||
chr3:138496779
|
C | T | 1 | a0002c0002t0002g0239 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1732+1252G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496779 | ||||||
chr3:138496935
|
T | G | 74 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0002g0002others(71): Show | 86 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1732+1096A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138496935 | ||||||
chr3:138497149
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1732+882A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497149 | ||||||
chr3:138497331
|
T | TA | 14 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(11): Show | 14 | HG00741.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1732+699dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497331 | ||||||
chr3:138497388
|
C | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1732+643G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497388 | ||||||
chr3:138497715
|
A | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1732+316T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497715 | ||||||
chr3:138497763
|
T | C | 1 | a0002c0002t0002g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1732+268A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497763 | ||||||
chr3:138497871
|
A | C | 24 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(21): Show | 26 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1732+160T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497871 | ||||||
chr3:138497890
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0142others(2): Show | 5 | HG02071.hp2 NA18947.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1732+141C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497890 | ||||||
chr3:138497928
|
C | G | 1 | a0003c0003t0003g0034 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1732+103G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 17/17 | chr3 | 138497928 | ||||||
chr3:138498244
|
TTTTC | T | 3 | a0002c0002t0002g0022a0002c0002t0002g0221a0002c0002t0002g0266 | 4 | HG01884.hp1 HG01884.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653-138_1653-135d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498244 | ||||||
chr3:138498383
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1653-273T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498383 | ||||||
chr3:138498576
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1653-466G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498576 | ||||||
chr3:138498578
|
C | T | 1 | a0003c0003t0003g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1653-468G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498578 | ||||||
chr3:138498683
|
C | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1653-573G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498683 | ||||||
chr3:138498897
|
T | G | 1 | a0003c0003t0001g0073 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1653-787A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498897 | ||||||
chr3:138498914
|
C | T | 2 | a0002c0002t0002g0036a0002c0002t0002g0037 | 2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1653-804G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138498914 | ||||||
chr3:138499146
|
C | T | 13 | a0003c0003t0003g0012a0003c0003t0003g0039a0003c0003t0003g0102others(10): Show | 14 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1652+964G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499146 | ||||||
chr3:138499169
|
G | C | 1 | a0002c0002t0001g0018 | 2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1652+941C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499169 | ||||||
chr3:138499266
|
T | TG | 72 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(69): Show | 77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1652+843dupC | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499266 | ||||||
chr3:138499357
|
T | A | 2 | a0003c0003t0003g0069a0003c0003t0003g0071 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1652+753A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499357 | ||||||
chr3:138499493
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1652+617T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499493 | ||||||
chr3:138499559
|
A | G | 1 | a0003c0003t0003g0093 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1652+551T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499559 | ||||||
chr3:138499724
|
C | T | 3 | a0002c0002t0001g0018a0002c0002t0001g0194a0002c0002t0001g0195 | 4 | HG02257.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1652+386G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499724 | ||||||
chr3:138499772
|
A | C | 1 | a0002c0002t0002g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1652+338T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499772 | ||||||
chr3:138499783
|
T | TAC | 5 | a0001c0001t0001g0126a0001c0001t0001g0276a0001c0004t0004g0215others(2): Show | 5 | HG01261.hp2 HG02071.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1652+325_1652+326d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACAC | 70 | a0001c0001t0001g0138a0003c0003t0001g0026a0003c0003t0001g0027others(67): Show | 74 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1652+323_1652+326d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACAC | 12 | a0002c0002t0002g0244a0003c0003t0003g0003a0003c0003t0003g0050others(9): Show | 14 | HG01243.hp2 HG02559.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1652+321_1652+326d others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACACA others(1): Show |
65 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(62): Show | 77 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1652+319_1652+326d others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACACA others(3): Show |
5 | a0002c0002t0002g0035a0002c0002t0002g0251a0002c0002t0002g0265others(2): Show | 5 | HG02027.hp1 HG02129.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1652+317_1652+326d others(12): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACACA others(5): Show |
1 | a0002c0002t0002g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1652+315_1652+326d others(14): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACACA others(11): Show |
16 | a0002c0002t0001g0018a0002c0002t0001g0196a0002c0002t0001g0197others(13): Show | 17 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1652+309_1652+326d others(20): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACACA others(13): Show |
5 | a0002c0002t0001g0019a0002c0002t0001g0194a0002c0002t0001g0195others(2): Show | 6 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1652+307_1652+326d others(22): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACACA others(17): Show |
2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1652+326_1652+327i others(26): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499783
|
T | TACACACA others(19): Show |
1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1652+326_1652+327i others(28): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499783 | ||||||
chr3:138499810
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1652+300A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499810 | ||||||
chr3:138499867
|
C | A | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1652+243G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138499867 | ||||||
chr3:138500076
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1652+34A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 16/17 | chr3 | 138500076 | ||||||
chr3:138500593
|
AAG | A | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1369-28_1369-27del others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/17 | chr3 | 138500593 | ||||||
chr3:138500725
|
T | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1368+10A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 14/17 | chr3 | 138500725 | ||||||
chr3:138501011
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1222-130G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501011 | ||||||
chr3:138501050
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1222-169A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501050 | ||||||
chr3:138501065
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-184G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501065 | ||||||
chr3:138501081
|
A | G | 59 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(56): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1222-200T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501081 | ||||||
chr3:138501295
|
T | A | 1 | a0003c0003t0003g0046 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222-414A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501295 | ||||||
chr3:138501296
|
C | G | 1 | a0003c0003t0003g0046 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1222-415G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501296 | ||||||
chr3:138501400
|
C | T | 3 | a0003c0003t0003g0052a0003c0003t0003g0053a0003c0003t0003g0092 | 3 | HG01256.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1222-519G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501400 | ||||||
chr3:138501432
|
T | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1222-551A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501432 | ||||||
chr3:138501482
|
A | G | 1 | a0003c0003t0003g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1222-601T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501482 | ||||||
chr3:138501498
|
G | C | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1222-617C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501498 | ||||||
chr3:138501528
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-647C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501528 | ||||||
chr3:138501588
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-707T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501588 | ||||||
chr3:138501652
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-771C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501652 | ||||||
chr3:138501664
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1222-783T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501664 | ||||||
chr3:138501737
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1222-856C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501737 | ||||||
chr3:138501747
|
G | A | 7 | a0003c0003t0003g0009a0003c0003t0003g0062a0003c0003t0003g0063others(4): Show | 8 | HG00140.hp1 HG03239.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222-866C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501747 | ||||||
chr3:138501897
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-1016A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138501897 | ||||||
chr3:138502010
|
T | C | 1 | a0002c0002t0002g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1222-1129A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502010 | ||||||
chr3:138502089
|
G | C | 2 | a0003c0003t0003g0076a0003c0003t0003g0091 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1222-1208C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502089 | ||||||
chr3:138502451
|
T | C | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1222-1570A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502451 | ||||||
chr3:138502539
|
GA | G | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(66): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1222-1659delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502539 | ||||||
chr3:138502744
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1222-1863G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502744 | ||||||
chr3:138502769
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1222-1888T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502769 | ||||||
chr3:138502840
|
C | A | 1 | a0003c0003t0003g0034 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1222-1959G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502840 | ||||||
chr3:138502846
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-1965G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502846 | ||||||
chr3:138502881
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1222-2000T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138502881 | ||||||
chr3:138503266
|
A | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1221+2029T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503266 | ||||||
chr3:138503338
|
A | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+1957T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503338 | ||||||
chr3:138503455
|
C | T | 6 | a0002c0002t0001g0019a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 7 | HG01123.hp2 HG01496.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1221+1840G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503455 | ||||||
chr3:138503552
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+1743A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503552 | ||||||
chr3:138503710
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+1585G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503710 | ||||||
chr3:138503884
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1221+1411G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138503884 | ||||||
chr3:138504155
|
A | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0119others(8): Show | 13 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1221+1140T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504155 | ||||||
chr3:138504172
|
A | G | 84 | a0001c0001t0001g0170a0001c0001t0001g0171a0003c0003t0001g0026others(81): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1221+1123T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504172 | ||||||
chr3:138504220
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1221+1075C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504220 | ||||||
chr3:138504279
|
G | A | 1 | a0002c0002t0002g0249 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1221+1016C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504279 | ||||||
chr3:138504282
|
T | G | 1 | a0002c0002t0002g0249 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1221+1013A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504282 | ||||||
chr3:138504283
|
A | G | 1 | a0002c0002t0002g0249 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1221+1012T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504283 | ||||||
chr3:138504439
|
T | C | 1 | a0002c0002t0002g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1221+856A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504439 | ||||||
chr3:138504825
|
G | T | 2 | a0003c0003t0003g0102a0003c0003t0003g0104 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1221+470C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504825 | ||||||
chr3:138504833
|
C | A | 2 | a0003c0003t0003g0102a0003c0003t0003g0104 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1221+462G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504833 | ||||||
chr3:138504841
|
C | CAGAAAAT others(15): Show |
1 | a0002c0002t0002g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1221+432_1221+453d others(24): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504841 | ||||||
chr3:138504863
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+432C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504863 | ||||||
chr3:138504917
|
G | A | 1 | a0003c0003t0003g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1221+378C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138504917 | ||||||
chr3:138505098
|
C | T | 1 | a0003c0003t0003g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1221+197G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138505098 | ||||||
chr3:138505181
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1221+114G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 13/17 | chr3 | 138505181 | ||||||
chr3:138505621
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1051-156A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505621 | ||||||
chr3:138505719
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1051-254G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505719 | ||||||
chr3:138505935
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0129a0001c0001t0001g0188 | 5 | HG01123.hp1 HG01257.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-470G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505935 | ||||||
chr3:138505960
|
A | G | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1051-495T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505960 | ||||||
chr3:138505964
|
C | T | 1 | a0001c0004t0004g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1051-499G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505964 | ||||||
chr3:138505978
|
C | T | 5 | a0003c0003t0003g0076a0003c0003t0003g0091a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01109.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-513G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138505978 | ||||||
chr3:138506058
|
ACTAT | A | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1051-597_1051-594d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506058 | ||||||
chr3:138506308
|
A | C | 4 | a0002c0002t0002g0237a0002c0002t0002g0257a0002c0002t0002g0258others(1): Show | 4 | HG00408.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-843T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506308 | ||||||
chr3:138506616
|
A | G | 2 | a0003c0003t0003g0010a0003c0003t0003g0011 | 4 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-1151T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506616 | ||||||
chr3:138506690
|
T | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1051-1225A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506690 | ||||||
chr3:138506697
|
A | T | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1051-1232T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506697 | ||||||
chr3:138506795
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1051-1330C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506795 | ||||||
chr3:138506824
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1051-1359C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506824 | ||||||
chr3:138506948
|
G | A | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1051-1483C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506948 | ||||||
chr3:138506953
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1050+1486C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138506953 | ||||||
chr3:138507068
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1050+1371G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507068 | ||||||
chr3:138507080
|
A | C | 1 | a0002c0002t0002g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1050+1359T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507080 | ||||||
chr3:138507507
|
A | G | 1 | a0003c0003t0001g0073 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1050+932T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507507 | ||||||
chr3:138507539
|
T | C | 1 | a0002c0002t0002g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1050+900A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507539 | ||||||
chr3:138507645
|
C | T | 1 | a0003c0003t0001g0060 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1050+794G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507645 | ||||||
chr3:138507832
|
GT | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+606delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507832 | ||||||
chr3:138507882
|
T | A | 1 | a0002c0002t0002g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1050+557A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507882 | ||||||
chr3:138507887
|
A | T | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1050+552T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507887 | ||||||
chr3:138507934
|
A | C | 4 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0001g0210others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050+505T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507934 | ||||||
chr3:138507992
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1050+447G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138507992 | ||||||
chr3:138508081
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+358C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508081 | ||||||
chr3:138508188
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+251C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508188 | ||||||
chr3:138508191
|
A | T | 163 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(160): Show | 181 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1050+248T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508191 | ||||||
chr3:138508347
|
T | A | 5 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243others(2): Show | 5 | NA18947.hp2 NA18949.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050+92A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 12/17 | chr3 | 138508347 | ||||||
chr3:138508709
|
A | G | 1 | a0003c0003t0003g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.945-165T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508709 | ||||||
chr3:138508729
|
A | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-185T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508729 | ||||||
chr3:138508736
|
A | T | 2 | a0003c0003t0003g0064a0003c0003t0003g0065 | 2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.945-192T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508736 | ||||||
chr3:138508737
|
T | A | 3 | a0003c0005t0003g0058a0003c0005t0003g0088a0003c0005t0003g0089 | 3 | HG02280.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.945-193A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508737 | ||||||
chr3:138508761
|
T | G | 1 | a0001c0001t0001g0017 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945-217A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508761 | ||||||
chr3:138508765
|
G | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-221C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508765 | ||||||
chr3:138508878
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.945-334G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508878 | ||||||
chr3:138508884
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-340G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138508884 | ||||||
chr3:138509011
|
G | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-467C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509011 | ||||||
chr3:138509013
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.945-469C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509013 | ||||||
chr3:138509101
|
T | G | 4 | a0002c0002t0001g0019a0002c0002t0001g0201a0002c0002t0001g0204others(1): Show | 5 | HG01123.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.945-557A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509101 | ||||||
chr3:138509163
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-619C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509163 | ||||||
chr3:138509225
|
C | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.945-681G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509225 | ||||||
chr3:138509255
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.945-711C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509255 | ||||||
chr3:138509359
|
A | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-815T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509359 | ||||||
chr3:138509518
|
A | G | 7 | a0002c0002t0002g0005a0002c0002t0002g0036a0002c0002t0002g0037others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.945-974T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509518 | ||||||
chr3:138509539
|
G | A | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.945-995C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509539 | ||||||
chr3:138509579
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-1035G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509579 | ||||||
chr3:138509852
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-1308T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509852 | ||||||
chr3:138509906
|
C | A | 182 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(179): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.945-1362G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509906 | ||||||
chr3:138509985
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-1441A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138509985 | ||||||
chr3:138510251
|
T | TA | 79 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(76): Show | 91 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.945-1708dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510251 | ||||||
chr3:138510276
|
T | C | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-1732A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510276 | ||||||
chr3:138510349
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.945-1805G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510349 | ||||||
chr3:138510433
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(81): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.945-1890dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510433 | ||||||
chr3:138510574
|
C | G | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.945-2030G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510574 | ||||||
chr3:138510636
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2092C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510636 | ||||||
chr3:138510662
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2118A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510662 | ||||||
chr3:138510719
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2175G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510719 | ||||||
chr3:138510772
|
G | C | 2 | a0002c0002t0002g0036a0002c0002t0002g0037 | 2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.945-2228C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510772 | ||||||
chr3:138510843
|
A | T | 2 | a0002c0002t0002g0036a0002c0002t0002g0037 | 2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.945-2299T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510843 | ||||||
chr3:138510856
|
C | CT | 7 | a0002c0002t0002g0035a0002c0002t0002g0227a0002c0002t0002g0242others(4): Show | 7 | HG00408.hp2 HG01256.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.945-2313dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510856 | ||||||
chr3:138510856
|
CT | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(100): Show | 116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.945-2313delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510856 | ||||||
chr3:138510883
|
C | T | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-2339G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510883 | ||||||
chr3:138510892
|
G | A | 5 | a0002c0002t0002g0223a0002c0002t0002g0225a0002c0002t0002g0226others(2): Show | 5 | HG02071.hp1 NA18747.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.945-2348C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138510892 | ||||||
chr3:138511026
|
T | TTTG | 183 | a0001c0001t0001g0134a0001c0004t0004g0109a0001c0004t0004g0110others(180): Show | 203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.945-2485_945-2483d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511026 | ||||||
chr3:138511060
|
A | G | 7 | a0002c0002t0002g0005a0002c0002t0002g0036a0002c0002t0002g0037others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.945-2516T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511060 | ||||||
chr3:138511163
|
G | GC | 23 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(20): Show | 27 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.945-2620dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511163 | ||||||
chr3:138511168
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.945-2624G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511168 | ||||||
chr3:138511245
|
C | A | 1 | a0003c0005t0003g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.945-2701G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511245 | ||||||
chr3:138511286
|
C | G | 2 | a0003c0003t0003g0084a0003c0003t0003g0085 | 2 | HG02004.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.945-2742G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511286 | ||||||
chr3:138511300
|
T | C | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.945-2756A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511300 | ||||||
chr3:138511337
|
T | C | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.945-2793A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511337 | ||||||
chr3:138511393
|
G | C | 3 | a0003c0003t0003g0043a0003c0003t0003g0047a0003c0003t0003g0048 | 3 | HG00621.hp1 HG00673.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.945-2849C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511393 | ||||||
chr3:138511473
|
C | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-2929G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511473 | ||||||
chr3:138511566
|
A | G | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.945-3022T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511566 | ||||||
chr3:138511604
|
C | T | 1 | a0003c0003t0003g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.945-3060G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511604 | ||||||
chr3:138511657
|
T | C | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-3113A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511657 | ||||||
chr3:138511788
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-3244T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138511788 | ||||||
chr3:138512113
|
T | C | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-3569A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512113 | ||||||
chr3:138512421
|
T | C | 67 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(64): Show | 79 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.945-3877A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512421 | ||||||
chr3:138512504
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.945-3960G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512504 | ||||||
chr3:138512576
|
C | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-4032G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512576 | ||||||
chr3:138512604
|
A | C | 1 | a0002c0002t0001g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.945-4060T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512604 | ||||||
chr3:138512620
|
T | C | 1 | a0003c0003t0003g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.945-4076A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512620 | ||||||
chr3:138512756
|
C | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-4212G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512756 | ||||||
chr3:138512796
|
A | G | 1 | a0002c0002t0002g0270 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.945-4252T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512796 | ||||||
chr3:138512893
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-4349G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512893 | ||||||
chr3:138512920
|
C | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-4376G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512920 | ||||||
chr3:138512980
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.945-4436T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138512980 | ||||||
chr3:138513231
|
C | A | 1 | a0002c0002t0001g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945-4687G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513231 | ||||||
chr3:138513373
|
C | G | 1 | a0001c0004t0004g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.945-4829G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513373 | ||||||
chr3:138513474
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.945-4930G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513474 | ||||||
chr3:138513525
|
T | TC | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.945-4982dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513525 | ||||||
chr3:138513563
|
G | A | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.945-5019C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513563 | ||||||
chr3:138513952
|
T | TA | 91 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.945-5409dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513952 | ||||||
chr3:138513965
|
C | A | 8 | a0003c0003t0001g0026a0003c0003t0001g0060a0003c0003t0001g0067others(5): Show | 8 | HG00639.hp1 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.945-5421G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138513965 | ||||||
chr3:138514004
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-5460C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514004 | ||||||
chr3:138514202
|
T | C | 2 | a0002c0002t0002g0021a0002c0002t0002g0235 | 3 | HG00544.hp1 HG00558.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.945-5658A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514202 | ||||||
chr3:138514234
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-5690C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514234 | ||||||
chr3:138514496
|
C | T | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.945-5952G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514496 | ||||||
chr3:138514781
|
G | C | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-6237C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514781 | ||||||
chr3:138514849
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.945-6305C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514849 | ||||||
chr3:138514877
|
T | C | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-6333A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514877 | ||||||
chr3:138514961
|
A | G | 80 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(77): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.945-6417T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138514961 | ||||||
chr3:138515039
|
G | A | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.945-6495C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515039 | ||||||
chr3:138515059
|
CAAG | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-6518_945-6516d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515059 | ||||||
chr3:138515062
|
G | C | 181 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(178): Show | 201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.945-6518C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515062 | ||||||
chr3:138515170
|
T | C | 1 | a0002c0002t0002g0036 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.945-6626A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515170 | ||||||
chr3:138515298
|
C | T | 1 | a0003c0003t0003g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.945-6754G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515298 | ||||||
chr3:138515404
|
C | G | 1 | a0002c0002t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.945-6860G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515404 | ||||||
chr3:138515467
|
C | CA | 87 | a0001c0001t0001g0136a0001c0001t0001g0153a0001c0001t0001g0170others(84): Show | 93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.945-6924dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | ||||||
chr3:138515467
|
C | CAA | 28 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0020others(25): Show | 34 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.945-6925_945-6924d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | ||||||
chr3:138515467
|
C | CAAA | 39 | a0002c0002t0002g0002a0002c0002t0002g0007a0002c0002t0002g0021others(36): Show | 45 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.945-6926_945-6924d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | ||||||
chr3:138515467
|
C | CAAAA | 8 | a0002c0002t0002g0038a0002c0002t0002g0225a0002c0002t0002g0228others(5): Show | 8 | HG01433.hp1 NA18968.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.945-6927_945-6924d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515467 | ||||||
chr3:138515471
|
A | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-6927T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515471 | ||||||
chr3:138515472
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-6928T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515472 | ||||||
chr3:138515569
|
GA | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7026delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515569 | ||||||
chr3:138515612
|
A | G | 180 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(177): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.945-7068T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515612 | ||||||
chr3:138515616
|
T | C | 1 | a0003c0003t0003g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.945-7072A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515616 | ||||||
chr3:138515684
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7140T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515684 | ||||||
chr3:138515725
|
C | T | 58 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(55): Show | 68 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.945-7181G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515725 | ||||||
chr3:138515734
|
C | T | 159 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0002g0002others(156): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.945-7190G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515734 | ||||||
chr3:138515756
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7212A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515756 | ||||||
chr3:138515763
|
G | A | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.945-7219C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515763 | ||||||
chr3:138515769
|
G | A | 2 | a0002c0002t0002g0261a0002c0002t0002g0265 | 2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.945-7225C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515769 | ||||||
chr3:138515872
|
A | G | 4 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031others(1): Show | 4 | HG00735.hp2 HG01243.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.945-7328T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515872 | ||||||
chr3:138515910
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-7366A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515910 | ||||||
chr3:138515941
|
C | G | 1 | a0002c0002t0002g0006 | 3 | HG02735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.945-7397G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515941 | ||||||
chr3:138515952
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7408G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138515952 | ||||||
chr3:138516102
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.945-7558G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516102 | ||||||
chr3:138516133
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-7589T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516133 | ||||||
chr3:138516136
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.945-7592C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516136 | ||||||
chr3:138516361
|
T | A | 3 | a0002c0002t0002g0229a0002c0002t0002g0230a0002c0002t0002g0231 | 3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.945-7817A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516361 | ||||||
chr3:138516385
|
T | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945-7841A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516385 | ||||||
chr3:138516393
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-7849G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516393 | ||||||
chr3:138516399
|
G | A | 1 | a0003c0003t0003g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.945-7855C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516399 | ||||||
chr3:138516410
|
G | A | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.945-7866C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516410 | ||||||
chr3:138516443
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.945-7899A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516443 | ||||||
chr3:138516535
|
A | AC | 9 | a0001c0001t0001g0159a0001c0001t0001g0185a0001c0001t0001g0275others(6): Show | 9 | HG00621.hp1 HG02080.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.945-7992dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516535 | ||||||
chr3:138516572
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.945-8028C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516572 | ||||||
chr3:138516616
|
A | G | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.945-8072T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516616 | ||||||
chr3:138516665
|
C | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.945-8121G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516665 | ||||||
chr3:138516750
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-8206C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516750 | ||||||
chr3:138516775
|
G | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.945-8231C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516775 | ||||||
chr3:138516797
|
CAT | C | 59 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(56): Show | 69 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.945-8255_945-8254d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516797 | ||||||
chr3:138516811
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.945-8267G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138516811 | ||||||
chr3:138517276
|
G | A | 6 | a0003c0003t0003g0052a0003c0003t0003g0053a0003c0003t0003g0055others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.944+8214C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517276 | ||||||
chr3:138517402
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+8088T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517402 | ||||||
chr3:138517449
|
C | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+8041G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517449 | ||||||
chr3:138517455
|
G | A | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.944+8035C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517455 | ||||||
chr3:138517578
|
A | G | 1 | a0002c0002t0002g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.944+7912T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517578 | ||||||
chr3:138517593
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7897G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517593 | ||||||
chr3:138517788
|
A | T | 91 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.944+7702T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517788 | ||||||
chr3:138517794
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7696C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517794 | ||||||
chr3:138517854
|
G | A | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.944+7636C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138517854 | ||||||
chr3:138518003
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.944+7487G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518003 | ||||||
chr3:138518011
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0193 | 2 | NA18957.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.944+7479C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518011 | ||||||
chr3:138518017
|
A | G | 180 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(177): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.944+7473T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518017 | ||||||
chr3:138518044
|
C | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7446G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518044 | ||||||
chr3:138518044
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+7446G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518044 | ||||||
chr3:138518117
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+7373G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518117 | ||||||
chr3:138518118
|
G | A | 1 | a0003c0003t0001g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.944+7372C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518118 | ||||||
chr3:138518132
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG01175.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.944+7358C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518132 | ||||||
chr3:138518151
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.944+7339C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518151 | ||||||
chr3:138518209
|
C | T | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.944+7281G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518209 | ||||||
chr3:138518323
|
T | C | 1 | a0002c0002t0002g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.944+7167A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518323 | ||||||
chr3:138518327
|
T | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+7163A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518327 | ||||||
chr3:138518350
|
G | A | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.944+7140C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518350 | ||||||
chr3:138518373
|
C | T | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.944+7117G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518373 | ||||||
chr3:138518789
|
A | T | 1 | a0002c0002t0002g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.944+6701T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518789 | ||||||
chr3:138518828
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+6662G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518828 | ||||||
chr3:138518845
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+6645C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518845 | ||||||
chr3:138518884
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0212 | 3 | HG02572.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.944+6606C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518884 | ||||||
chr3:138518903
|
G | C | 1 | a0002c0002t0002g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.944+6587C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138518903 | ||||||
chr3:138519057
|
C | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+6433G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519057 | ||||||
chr3:138519158
|
G | T | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.944+6332C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519158 | ||||||
chr3:138519225
|
C | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+6265G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519225 | ||||||
chr3:138519236
|
G | C | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.944+6254C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519236 | ||||||
chr3:138519253
|
ACT | A | 80 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(77): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.944+6235_944+6236d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519253 | ||||||
chr3:138519260
|
A | C | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.944+6230T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519260 | ||||||
chr3:138519262
|
T | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+6228A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519262 | ||||||
chr3:138519314
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+6176G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519314 | ||||||
chr3:138519459
|
G | T | 1 | a0003c0003t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.944+6031C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519459 | ||||||
chr3:138519568
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5922G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519568 | ||||||
chr3:138519589
|
A | G | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.944+5901T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519589 | ||||||
chr3:138519611
|
C | A | 3 | a0003c0003t0003g0098a0003c0003t0003g0099a0003c0003t0003g0100 | 3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.944+5879G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519611 | ||||||
chr3:138519639
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.944+5851A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519639 | ||||||
chr3:138519707
|
G | A | 5 | a0001c0001t0001g0157a0003c0003t0003g0056a0003c0005t0003g0078others(2): Show | 5 | HG02451.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+5783C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519707 | ||||||
chr3:138519726
|
T | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5764A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519726 | ||||||
chr3:138519729
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.944+5761A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519729 | ||||||
chr3:138519738
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5752T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519738 | ||||||
chr3:138519747
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5743C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519747 | ||||||
chr3:138519778
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+5712G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138519778 | ||||||
chr3:138520109
|
C | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5381G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520109 | ||||||
chr3:138520230
|
A | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+5260T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520230 | ||||||
chr3:138520233
|
G | A | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.944+5257C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520233 | ||||||
chr3:138520329
|
G | A | 4 | a0001c0001t0001g0173a0004c0006t0005g0028a0004c0006t0005g0030others(1): Show | 4 | HG00735.hp2 HG01891.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+5161C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520329 | ||||||
chr3:138520347
|
C | T | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.944+5143G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520347 | ||||||
chr3:138520355
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+5135A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520355 | ||||||
chr3:138520362
|
C | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+5128G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520362 | ||||||
chr3:138520463
|
T | C | 180 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(177): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.944+5027A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520463 | ||||||
chr3:138520542
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+4948G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520542 | ||||||
chr3:138520683
|
A | G | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.944+4807T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520683 | ||||||
chr3:138520827
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4663G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520827 | ||||||
chr3:138520933
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4557A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520933 | ||||||
chr3:138520947
|
T | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+4543A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520947 | ||||||
chr3:138520966
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0118 | 3 | NA18961.hp1 NA19064.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.944+4524C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138520966 | ||||||
chr3:138521056
|
T | C | 180 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(177): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.944+4434A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521056 | ||||||
chr3:138521057
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+4433C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521057 | ||||||
chr3:138521069
|
C | T | 3 | a0002c0002t0002g0229a0002c0002t0002g0230a0002c0002t0002g0231 | 3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.944+4421G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521069 | ||||||
chr3:138521221
|
G | A | 2 | a0002c0002t0001g0205a0004c0006t0005g0030 | 2 | HG00735.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.944+4269C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521221 | ||||||
chr3:138521225
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4265T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521225 | ||||||
chr3:138521251
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+4239C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521251 | ||||||
chr3:138521344
|
A | AC | 12 | a0001c0001t0001g0134a0001c0001t0001g0149a0001c0001t0001g0159others(9): Show | 12 | HG01243.hp1 HG01516.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.944+4145dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521344 | ||||||
chr3:138521349
|
G | A | 2 | a0003c0003t0003g0105a0003c0003t0003g0108 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.944+4141C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521349 | ||||||
chr3:138521367
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.944+4123C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521367 | ||||||
chr3:138521388
|
A | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+4102T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521388 | ||||||
chr3:138521401
|
G | A | 1 | a0002c0002t0002g0253 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.944+4089C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521401 | ||||||
chr3:138521420
|
G | A | 1 | a0003c0003t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.944+4070C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521420 | ||||||
chr3:138521441
|
G | A | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+4049C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521441 | ||||||
chr3:138521492
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3998A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521492 | ||||||
chr3:138521535
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.944+3955G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521535 | ||||||
chr3:138521570
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3920C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521570 | ||||||
chr3:138521577
|
T | C | 182 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(179): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.944+3913A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521577 | ||||||
chr3:138521578
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.944+3912C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521578 | ||||||
chr3:138521645
|
C | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+3845G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521645 | ||||||
chr3:138521649
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3841G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521649 | ||||||
chr3:138521657
|
C | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+3833G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521657 | ||||||
chr3:138521676
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.944+3814C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521676 | ||||||
chr3:138521685
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+3805G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521685 | ||||||
chr3:138521694
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3796G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521694 | ||||||
chr3:138521771
|
C | T | 1 | a0002c0002t0002g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.944+3719G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521771 | ||||||
chr3:138521808
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3682T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521808 | ||||||
chr3:138521825
|
C | T | 1 | a0002c0002t0002g0270 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.944+3665G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138521825 | ||||||
chr3:138522007
|
C | T | 66 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(63): Show | 78 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.944+3483G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522007 | ||||||
chr3:138522044
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+3446C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522044 | ||||||
chr3:138522091
|
C | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+3399G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522091 | ||||||
chr3:138522105
|
C | T | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.944+3385G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522105 | ||||||
chr3:138522117
|
T | C | 180 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(177): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.944+3373A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522117 | ||||||
chr3:138522294
|
TA | T | 77 | a0001c0001t0001g0141a0001c0001t0001g0282a0002c0002t0002g0002others(74): Show | 89 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.944+3195delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522294 | ||||||
chr3:138522462
|
T | C | 1 | a0002c0002t0002g0262 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.944+3028A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522462 | ||||||
chr3:138522517
|
C | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+2973G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522517 | ||||||
chr3:138522518
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+2972C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522518 | ||||||
chr3:138522522
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+2968G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522522 | ||||||
chr3:138522563
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+2927T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522563 | ||||||
chr3:138522578
|
G | A | 80 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(77): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.944+2912C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522578 | ||||||
chr3:138522602
|
G | A | 1 | a0002c0002t0002g0274 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.944+2888C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522602 | ||||||
chr3:138522681
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(81): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.944+2809A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522681 | ||||||
chr3:138522859
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+2631A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522859 | ||||||
chr3:138522992
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+2498C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138522992 | ||||||
chr3:138523099
|
T | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+2391A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523099 | ||||||
chr3:138523158
|
T | C | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+2332A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523158 | ||||||
chr3:138523174
|
AC | A | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.944+2315delG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523174 | ||||||
chr3:138523176
|
C | G | 2 | a0003c0005t0003g0058a0003c0005t0003g0089 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.944+2314G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523176 | ||||||
chr3:138523379
|
A | G | 1 | a0002c0002t0002g0270 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.944+2111T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523379 | ||||||
chr3:138523442
|
T | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+2048A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523442 | ||||||
chr3:138523479
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.944+2011A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523479 | ||||||
chr3:138523506
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1984A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523506 | ||||||
chr3:138523542
|
T | C | 1 | a0002c0002t0002g0237 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.944+1948A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523542 | ||||||
chr3:138523649
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.944+1841G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523649 | ||||||
chr3:138523664
|
C | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1826G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523664 | ||||||
chr3:138523667
|
G | T | 1 | a0002c0002t0002g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.944+1823C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523667 | ||||||
chr3:138523671
|
C | T | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.944+1819G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523671 | ||||||
chr3:138523734
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1756G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523734 | ||||||
chr3:138523780
|
G | A | 1 | a0003c0003t0003g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.944+1710C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523780 | ||||||
chr3:138523843
|
C | A | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+1647G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523843 | ||||||
chr3:138523849
|
T | C | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+1641A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523849 | ||||||
chr3:138523907
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1583C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523907 | ||||||
chr3:138523908
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+1582G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523908 | ||||||
chr3:138523975
|
T | C | 1 | a0001c0004t0006g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.944+1515A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138523975 | ||||||
chr3:138524005
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.944+1485A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524005 | ||||||
chr3:138524026
|
T | G | 182 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(179): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.944+1464A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524026 | ||||||
chr3:138524028
|
C | T | 181 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(178): Show | 199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.944+1462G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524028 | ||||||
chr3:138524034
|
A | C | 182 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(179): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.944+1456T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524034 | ||||||
chr3:138524077
|
A | T | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.944+1413T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524077 | ||||||
chr3:138524135
|
T | C | 1 | a0001c0001t0001g0016 | 2 | HG01255.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.944+1355A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524135 | ||||||
chr3:138524207
|
C | T | 1 | a0003c0003t0003g0034 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.944+1283G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524207 | ||||||
chr3:138524388
|
A | C | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.944+1102T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524388 | ||||||
chr3:138524591
|
C | A | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.944+899G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524591 | ||||||
chr3:138524600
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+890T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524600 | ||||||
chr3:138524654
|
C | T | 4 | a0003c0003t0003g0097a0003c0003t0003g0098a0003c0003t0003g0099others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+836G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524654 | ||||||
chr3:138524775
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+715T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524775 | ||||||
chr3:138524797
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+693G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524797 | ||||||
chr3:138524811
|
T | C | 1 | a0002c0002t0002g0237 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.944+679A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524811 | ||||||
chr3:138524953
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+537C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138524953 | ||||||
chr3:138525019
|
G | A | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+471C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525019 | ||||||
chr3:138525024
|
A | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.944+466T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525024 | ||||||
chr3:138525158
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.944+332C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525158 | ||||||
chr3:138525184
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(81): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.944+306A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525184 | ||||||
chr3:138525270
|
G | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+220C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525270 | ||||||
chr3:138525303
|
T | C | 1 | a0002c0002t0002g0229 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.944+187A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525303 | ||||||
chr3:138525305
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+185G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525305 | ||||||
chr3:138525334
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.944+156A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525334 | ||||||
chr3:138525343
|
A | C | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.944+147T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525343 | ||||||
chr3:138525385
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.944+105C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525385 | ||||||
chr3:138525393
|
A | G | 1 | a0002c0002t0002g0272 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.944+97T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 11/17 | chr3 | 138525393 | ||||||
chr3:138525599
|
T | A | 1 | a0002c0002t0001g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.870-35A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525599 | ||||||
chr3:138525670
|
C | G | 1 | a0002c0002t0002g0220 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.870-106G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525670 | ||||||
chr3:138525699
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.870-135G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525699 | ||||||
chr3:138525770
|
C | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.870-206G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525770 | ||||||
chr3:138525842
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-278T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525842 | ||||||
chr3:138525870
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.870-306G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138525870 | ||||||
chr3:138526086
|
G | C | 21 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(18): Show | 23 | HG00639.hp1 HG01071.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.870-522C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526086 | ||||||
chr3:138526302
|
C | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-738G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526302 | ||||||
chr3:138526344
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-780C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526344 | ||||||
chr3:138526354
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.870-790C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526354 | ||||||
chr3:138526379
|
GT | G | 161 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(158): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.870-816delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526379 | ||||||
chr3:138526410
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-846A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526410 | ||||||
chr3:138526452
|
C | T | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.870-888G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526452 | ||||||
chr3:138526749
|
C | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.870-1185G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526749 | ||||||
chr3:138526936
|
T | C | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.870-1372A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526936 | ||||||
chr3:138526982
|
A | C | 80 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(77): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.870-1418T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138526982 | ||||||
chr3:138527011
|
CA | C | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.870-1448delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527011 | ||||||
chr3:138527166
|
TTTTTG | T | 3 | a0003c0003t0003g0010a0003c0003t0003g0011a0007c0009t0004g0217 | 5 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-1607_870-1603d others(7): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527166 | ||||||
chr3:138527187
|
A | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(96): Show | 112 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.870-1623T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527187 | ||||||
chr3:138527188
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.870-1624C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527188 | ||||||
chr3:138527195
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-1631T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527195 | ||||||
chr3:138527270
|
A | ATCT | 180 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(177): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.870-1709_870-1707d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527270 | ||||||
chr3:138527329
|
A | AT | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(84): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.870-1766dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527329 | ||||||
chr3:138527382
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+1817G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527382 | ||||||
chr3:138527470
|
G | A | 68 | a0001c0001t0001g0123a0002c0002t0002g0002a0002c0002t0002g0005others(65): Show | 80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.869+1729C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527470 | ||||||
chr3:138527496
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+1703G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527496 | ||||||
chr3:138527576
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0161a0001c0001t0001g0191 | 3 | NA18967.hp2 NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.869+1623G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527576 | ||||||
chr3:138527600
|
A | G | 1 | a0003c0003t0003g0042 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.869+1599T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527600 | ||||||
chr3:138527602
|
A | G | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.869+1597T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527602 | ||||||
chr3:138527641
|
C | A | 1 | a0001c0004t0004g0110 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.869+1558G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527641 | ||||||
chr3:138527690
|
G | A | 1 | a0003c0003t0003g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.869+1509C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527690 | ||||||
chr3:138527694
|
C | CA | 6 | a0001c0001t0001g0149a0001c0001t0001g0277a0004c0006t0005g0028others(3): Show | 6 | HG00735.hp2 HG01175.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+1504dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | ||||||
chr3:138527694
|
CA | C | 100 | a0001c0001t0001g0156a0001c0001t0001g0164a0001c0001t0001g0167others(97): Show | 107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.869+1504delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | ||||||
chr3:138527694
|
CAA | C | 7 | a0002c0002t0002g0037a0002c0002t0002g0229a0003c0003t0001g0072others(4): Show | 7 | HG01257.hp2 HG01891.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.869+1503_869+1504d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | ||||||
chr3:138527694
|
CAAA | C | 68 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(65): Show | 80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.869+1502_869+1504d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527694 | ||||||
chr3:138527843
|
T | A | 1 | a0001c0001t0001g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.869+1356A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527843 | ||||||
chr3:138527861
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+1338G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138527861 | ||||||
chr3:138528045
|
G | GT | 10 | a0001c0001t0001g0118a0001c0001t0001g0137a0001c0001t0001g0139others(7): Show | 10 | HG00673.hp1 HG01261.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.869+1153dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528045 | ||||||
chr3:138528457
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.869+742C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528457 | ||||||
chr3:138528541
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.869+658A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528541 | ||||||
chr3:138528629
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.869+570G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528629 | ||||||
chr3:138528749
|
TG | T | 180 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(177): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.869+449delC | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528749 | ||||||
chr3:138528884
|
C | T | 1 | a0003c0003t0003g0043 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.869+315G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528884 | ||||||
chr3:138528954
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+245A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528954 | ||||||
chr3:138528993
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+206C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138528993 | ||||||
chr3:138529012
|
T | A | 182 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(179): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.869+187A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138529012 | ||||||
chr3:138529079
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.869+120A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138529079 | ||||||
chr3:138529167
|
G | GA | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(66): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.869+31dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 10/17 | chr3 | 138529167 | ||||||
chr3:138529336
|
TTTA | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.780+36_780+38delTA others(1): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 9/17 | chr3 | 138529336 | ||||||
chr3:138529599
|
G | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.693-137C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529599 | ||||||
chr3:138529746
|
A | T | 1 | a0004c0006t0005g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.693-284T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529746 | ||||||
chr3:138529803
|
C | G | 1 | a0002c0002t0002g0229 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.693-341G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529803 | ||||||
chr3:138529922
|
T | C | 1 | a0003c0003t0003g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.693-460A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529922 | ||||||
chr3:138529943
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.693-481A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138529943 | ||||||
chr3:138530032
|
T | G | 1 | a0003c0003t0003g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.693-570A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530032 | ||||||
chr3:138530153
|
A | G | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.693-691T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530153 | ||||||
chr3:138530226
|
T | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.693-764A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530226 | ||||||
chr3:138530416
|
C | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.693-954G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530416 | ||||||
chr3:138530506
|
A | AAAC | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.693-1047_693-1045d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530506 | ||||||
chr3:138530541
|
T | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.693-1079A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530541 | ||||||
chr3:138530684
|
C | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.693-1222G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530684 | ||||||
chr3:138530795
|
A | G | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.693-1333T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138530795 | ||||||
chr3:138531250
|
T | G | 1 | a0002c0002t0002g0245 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.692+1264A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531250 | ||||||
chr3:138531280
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.692+1234T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531280 | ||||||
chr3:138531281
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.692+1233G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531281 | ||||||
chr3:138531383
|
A | G | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.692+1131T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531383 | ||||||
chr3:138531472
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.692+1042C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531472 | ||||||
chr3:138531591
|
G | A | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.692+923C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531591 | ||||||
chr3:138531683
|
T | G | 1 | a0002c0002t0002g0262 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.692+831A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531683 | ||||||
chr3:138531698
|
C | CT | 10 | a0001c0001t0001g0116a0001c0001t0001g0132a0001c0001t0001g0155others(7): Show | 10 | HG01069.hp1 HG01109.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.692+815dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531698 | ||||||
chr3:138531698
|
C | CTT | 74 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0067others(71): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.692+814_692+815dup others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531698 | ||||||
chr3:138531698
|
CT | C | 67 | a0001c0004t0004g0109a0001c0004t0004g0110a0002c0002t0002g0002others(64): Show | 79 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.692+815delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531698 | ||||||
chr3:138531732
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.692+782A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531732 | ||||||
chr3:138531736
|
G | A | 1 | a0002c0002t0001g0209 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.692+778C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138531736 | ||||||
chr3:138532054
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.692+460A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532054 | ||||||
chr3:138532156
|
A | G | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.692+358T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532156 | ||||||
chr3:138532424
|
T | C | 2 | a0003c0003t0003g0003a0003c0003t0003g0077 | 4 | HG02630.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.692+90A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532424 | ||||||
chr3:138532460
|
G | T | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.692+54C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532460 | ||||||
chr3:138532469
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.692+45T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532469 | ||||||
chr3:138532501
|
G | C | 1 | a0004c0006t0005g0030 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.692+13C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 8/17 | chr3 | 138532501 | ||||||
chr3:138532605
|
CGGTAT | C | 85 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(82): Show | 91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.636-40_636-36delAT others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532605 | ||||||
chr3:138532677
|
A | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.636-107T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532677 | ||||||
chr3:138532914
|
A | G | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-344T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532914 | ||||||
chr3:138532984
|
A | G | 2 | a0003c0003t0003g0057a0003c0003t0003g0059 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.636-414T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138532984 | ||||||
chr3:138533212
|
C | T | 1 | a0003c0003t0003g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.636-642G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533212 | ||||||
chr3:138533326
|
G | C | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.636-756C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533326 | ||||||
chr3:138533368
|
G | A | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.636-798C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533368 | ||||||
chr3:138533590
|
C | T | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.636-1020G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533590 | ||||||
chr3:138533672
|
A | C | 1 | a0003c0005t0003g0088 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.636-1102T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533672 | ||||||
chr3:138533699
|
G | C | 3 | a0003c0005t0003g0078a0003c0005t0003g0079a0003c0005t0003g0080 | 3 | HG02451.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.636-1129C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533699 | ||||||
chr3:138533812
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.636-1242T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533812 | ||||||
chr3:138533846
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.636-1276C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533846 | ||||||
chr3:138533909
|
C | T | 59 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(56): Show | 69 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.636-1339G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138533909 | ||||||
chr3:138534020
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.636-1450C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534020 | ||||||
chr3:138534079
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.636-1509G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534079 | ||||||
chr3:138534336
|
C | T | 1 | a0003c0003t0003g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.636-1766G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534336 | ||||||
chr3:138534490
|
G | T | 1 | a0001c0001t0001g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.636-1920C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534490 | ||||||
chr3:138534577
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.636-2007A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534577 | ||||||
chr3:138534603
|
T | C | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-2033A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534603 | ||||||
chr3:138534613
|
C | T | 1 | a0001c0004t0006g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.636-2043G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534613 | ||||||
chr3:138534758
|
T | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.636-2188A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534758 | ||||||
chr3:138534773
|
T | C | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.636-2203A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534773 | ||||||
chr3:138534785
|
T | C | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.636-2215A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534785 | ||||||
chr3:138534801
|
C | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-2231G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534801 | ||||||
chr3:138534867
|
T | C | 1 | a0002c0002t0002g0262 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.636-2297A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534867 | ||||||
chr3:138534969
|
A | G | 1 | a0002c0002t0002g0238 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.635+2209T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138534969 | ||||||
chr3:138535163
|
A | T | 1 | a0002c0002t0001g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.635+2015T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535163 | ||||||
chr3:138535192
|
C | G | 1 | a0002c0012t0002g0268 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.635+1986G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535192 | ||||||
chr3:138535276
|
T | G | 1 | a0002c0002t0002g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.635+1902A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535276 | ||||||
chr3:138535436
|
A | G | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.635+1742T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535436 | ||||||
chr3:138535528
|
C | T | 1 | a0003c0003t0003g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.635+1650G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535528 | ||||||
chr3:138535529
|
G | A | 7 | a0002c0002t0002g0005a0002c0002t0002g0036a0002c0002t0002g0037others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.635+1649C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535529 | ||||||
chr3:138535795
|
CTCT | C | 5 | a0001c0001t0001g0131a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 5 | HG00140.hp2 HG01167.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+1380_635+1382d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535795 | ||||||
chr3:138535808
|
C | T | 1 | a0003c0003t0003g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.635+1370G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535808 | ||||||
chr3:138535852
|
T | C | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.635+1326A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535852 | ||||||
chr3:138535855
|
C | T | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.635+1323G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535855 | ||||||
chr3:138535876
|
A | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+1302T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138535876 | ||||||
chr3:138536067
|
T | A | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.635+1111A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536067 | ||||||
chr3:138536236
|
T | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+942A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536236 | ||||||
chr3:138536356
|
C | T | 87 | a0001c0004t0006g0029a0001c0004t0006g0032a0003c0003t0001g0026others(84): Show | 93 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.635+822G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536356 | ||||||
chr3:138536375
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+803T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536375 | ||||||
chr3:138536498
|
T | C | 2 | a0002c0002t0001g0194a0002c0002t0001g0195 | 2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.635+680A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536498 | ||||||
chr3:138536538
|
A | G | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635+640T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536538 | ||||||
chr3:138536540
|
G | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+638C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536540 | ||||||
chr3:138536563
|
C | T | 161 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(158): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.635+615G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536563 | ||||||
chr3:138536616
|
T | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.635+562A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536616 | ||||||
chr3:138536679
|
G | A | 159 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0002g0002others(156): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.635+499C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536679 | ||||||
chr3:138536776
|
T | C | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.635+402A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536776 | ||||||
chr3:138536868
|
C | T | 161 | a0001c0004t0004g0215a0001c0004t0004g0216a0001c0004t0006g0029others(158): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.635+310G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536868 | ||||||
chr3:138536910
|
T | C | 2 | a0003c0003t0003g0010a0003c0003t0003g0011 | 4 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+268A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138536910 | ||||||
chr3:138537001
|
C | CA | 19 | a0001c0001t0001g0118a0001c0001t0001g0133a0001c0001t0001g0137others(16): Show | 19 | HG00544.hp2 HG00735.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.635+176dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537001 | ||||||
chr3:138537001
|
C | CAA | 120 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(117): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.635+175_635+176dup others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537001 | ||||||
chr3:138537001
|
C | CAAA | 30 | a0002c0002t0002g0005a0002c0002t0002g0025a0002c0002t0002g0037others(27): Show | 32 | HG00621.hp1 HG00673.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.635+174_635+176dup others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537001 | ||||||
chr3:138537061
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+117T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537061 | ||||||
chr3:138537139
|
A | T | 2 | a0003c0003t0003g0107a0003c0003t0003g0213 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.635+39T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 7/17 | chr3 | 138537139 | ||||||
chr3:138537410
|
G | A | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.466-63C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537410 | ||||||
chr3:138537458
|
C | T | 1 | a0003c0003t0003g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-111G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537458 | ||||||
chr3:138537536
|
A | G | 3 | a0002c0002t0002g0224a0002c0002t0002g0254a0002c0002t0002g0255 | 3 | NA19054.hp2 NA19063.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.466-189T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537536 | ||||||
chr3:138537582
|
G | A | 161 | a0001c0004t0004g0215a0001c0004t0004g0216a0001c0004t0006g0029others(158): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.466-235C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537582 | ||||||
chr3:138537583
|
T | C | 1 | a0002c0002t0002g0252 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.466-236A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537583 | ||||||
chr3:138537656
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-309C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537656 | ||||||
chr3:138537927
|
G | C | 1 | a0002c0002t0002g0253 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466-580C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537927 | ||||||
chr3:138537928
|
A | C | 1 | a0002c0002t0002g0253 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466-581T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537928 | ||||||
chr3:138537929
|
T | C | 1 | a0002c0002t0002g0253 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.466-582A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138537929 | ||||||
chr3:138538112
|
G | A | 1 | a0003c0003t0001g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.466-765C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538112 | ||||||
chr3:138538165
|
T | C | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.466-818A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538165 | ||||||
chr3:138538168
|
A | G | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-821T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538168 | ||||||
chr3:138538173
|
A | C | 14 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(11): Show | 16 | HG00738.hp2 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.466-826T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538173 | ||||||
chr3:138538208
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.466-861T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538208 | ||||||
chr3:138538391
|
A | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1044T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538391 | ||||||
chr3:138538482
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.466-1135G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538482 | ||||||
chr3:138538686
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.466-1339C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538686 | ||||||
chr3:138538695
|
T | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1348A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138538695 | ||||||
chr3:138539021
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-1674C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539021 | ||||||
chr3:138539170
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-1823C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539170 | ||||||
chr3:138539496
|
A | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-2149T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539496 | ||||||
chr3:138539554
|
G | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-2207C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539554 | ||||||
chr3:138539676
|
C | A | 1 | a0002c0002t0001g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.466-2329G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539676 | ||||||
chr3:138539699
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-2352A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138539699 | ||||||
chr3:138540004
|
A | G | 1 | a0002c0002t0002g0229 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.466-2657T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540004 | ||||||
chr3:138540065
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0129a0001c0001t0001g0188others(5): Show | 10 | HG00735.hp2 HG01123.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-2718C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540065 | ||||||
chr3:138540095
|
G | A | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.466-2748C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540095 | ||||||
chr3:138540223
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-2876C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540223 | ||||||
chr3:138540228
|
C | T | 1 | a0003c0003t0003g0093 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.466-2881G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540228 | ||||||
chr3:138540304
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466-2957C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540304 | ||||||
chr3:138540412
|
A | AC | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-3066dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540412 | ||||||
chr3:138540466
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466-3119T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540466 | ||||||
chr3:138540480
|
T | TA | 18 | a0001c0001t0001g0040a0001c0001t0001g0128a0001c0001t0001g0132others(15): Show | 18 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.466-3134dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540480 | ||||||
chr3:138540480
|
TAA | T | 154 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0002g0002others(151): Show | 172 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.466-3135_466-3134d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540480 | ||||||
chr3:138540609
|
G | T | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-3262C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540609 | ||||||
chr3:138540707
|
G | A | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-3360C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540707 | ||||||
chr3:138540892
|
C | A | 2 | a0003c0003t0003g0057a0003c0003t0003g0059 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.466-3545G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540892 | ||||||
chr3:138540962
|
C | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-3615G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540962 | ||||||
chr3:138540975
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-3628T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138540975 | ||||||
chr3:138541196
|
C | T | 12 | a0003c0003t0003g0034a0003c0003t0003g0041a0003c0003t0003g0042others(9): Show | 12 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-3849G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541196 | ||||||
chr3:138541394
|
G | A | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.466-4047C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541394 | ||||||
chr3:138541430
|
G | GA | 82 | a0001c0001t0001g0159a0003c0003t0001g0026a0003c0003t0001g0027others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-4084dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541430 | ||||||
chr3:138541430
|
GA | G | 74 | a0001c0001t0001g0134a0002c0002t0001g0207a0002c0002t0002g0002others(71): Show | 86 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.466-4084delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541430 | ||||||
chr3:138541625
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.466-4278A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541625 | ||||||
chr3:138541636
|
G | T | 28 | a0003c0003t0003g0009a0003c0003t0003g0050a0003c0003t0003g0052others(25): Show | 29 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-4289C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541636 | ||||||
chr3:138541941
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-4594T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138541941 | ||||||
chr3:138542108
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-4761C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542108 | ||||||
chr3:138542446
|
G | A | 80 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(77): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.466-5099C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542446 | ||||||
chr3:138542576
|
G | C | 1 | a0002c0002t0002g0237 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.466-5229C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542576 | ||||||
chr3:138542583
|
G | A | 1 | a0003c0003t0001g0060 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.466-5236C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542583 | ||||||
chr3:138542720
|
C | T | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-5373G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542720 | ||||||
chr3:138542739
|
G | A | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-5392C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542739 | ||||||
chr3:138542965
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466-5618C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542965 | ||||||
chr3:138542974
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.466-5627C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138542974 | ||||||
chr3:138543085
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.466-5738C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543085 | ||||||
chr3:138543251
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-5904T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543251 | ||||||
chr3:138543398
|
C | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-6051G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543398 | ||||||
chr3:138543610
|
C | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-6263G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543610 | ||||||
chr3:138543629
|
T | C | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-6282A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543629 | ||||||
chr3:138543636
|
C | A | 1 | a0002c0002t0002g0274 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.466-6289G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543636 | ||||||
chr3:138543696
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6349A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543696 | ||||||
chr3:138543839
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6492A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543839 | ||||||
chr3:138543972
|
G | A | 74 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0002g0002others(71): Show | 86 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.466-6625C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543972 | ||||||
chr3:138543989
|
T | TCTATTTA others(477): Show |
2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-6643_466-6642i others(486): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138543989 | ||||||
chr3:138544110
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-6763T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544110 | ||||||
chr3:138544133
|
C | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-6786G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544133 | ||||||
chr3:138544225
|
A | AAAAAAAA others(475): Show |
2 | a0001c0004t0006g0032a0004c0006t0005g0028 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.466-6879_466-6878i others(484): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544225 | ||||||
chr3:138544233
|
A | G | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.466-6886T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544233 | ||||||
chr3:138544307
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.466-6960G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544307 | ||||||
chr3:138544357
|
C | CAAAAAAA others(483): Show |
1 | a0001c0004t0006g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.466-7011_466-7010i others(492): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544357 | ||||||
chr3:138544357
|
CA | C | 176 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(173): Show | 196 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.466-7011delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544357 | ||||||
chr3:138544507
|
G | C | 1 | a0004c0006t0005g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.466-7160C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544507 | ||||||
chr3:138544509
|
G | GTGTA | 84 | a0001c0001t0001g0112a0001c0001t0001g0166a0001c0001t0001g0277others(81): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.466-7166_466-7163d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | ||||||
chr3:138544509
|
G | GTGTATGT others(1): Show |
5 | a0003c0003t0003g0039a0003c0003t0003g0064a0003c0003t0003g0065others(2): Show | 5 | HG01496.hp1 HG02622.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-7170_466-7163d others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | ||||||
chr3:138544509
|
G | GTGTATGT others(5): Show |
2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-7174_466-7163d others(14): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | ||||||
chr3:138544509
|
GTGTA | G | 4 | a0001c0004t0004g0215a0001c0004t0004g0216a0006c0010t0004g0023others(1): Show | 4 | HG01243.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-7166_466-7163d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544509 | ||||||
chr3:138544537
|
A | G | 2 | a0002c0002t0002g0241a0002c0002t0002g0242 | 2 | NA18949.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.466-7190T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544537 | ||||||
chr3:138544804
|
G | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7457C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544804 | ||||||
chr3:138544873
|
G | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7526C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544873 | ||||||
chr3:138544883
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.466-7536G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544883 | ||||||
chr3:138544888
|
G | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-7541C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544888 | ||||||
chr3:138544899
|
C | T | 1 | a0003c0003t0003g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.466-7552G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138544899 | ||||||
chr3:138545018
|
C | A | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.466-7671G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545018 | ||||||
chr3:138545048
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7701C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545048 | ||||||
chr3:138545184
|
C | T | 1 | a0002c0002t0002g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.466-7837G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545184 | ||||||
chr3:138545205
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.466-7858A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545205 | ||||||
chr3:138545653
|
T | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8306A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545653 | ||||||
chr3:138545815
|
T | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8468A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545815 | ||||||
chr3:138545914
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8567A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545914 | ||||||
chr3:138545948
|
C | T | 1 | a0002c0002t0002g0237 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.466-8601G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138545948 | ||||||
chr3:138546042
|
T | G | 2 | a0003c0003t0003g0010a0003c0003t0003g0011 | 4 | HG01175.hp1 HG01433.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-8695A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546042 | ||||||
chr3:138546134
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466-8787G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546134 | ||||||
chr3:138546259
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-8912G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546259 | ||||||
chr3:138546348
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.466-9001A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546348 | ||||||
chr3:138546549
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-9202C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546549 | ||||||
chr3:138546578
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-9231C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546578 | ||||||
chr3:138546593
|
A | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-9246T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546593 | ||||||
chr3:138546610
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-9263C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546610 | ||||||
chr3:138546612
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-9265T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546612 | ||||||
chr3:138546738
|
G | A | 7 | a0002c0002t0002g0002a0002c0002t0002g0224a0002c0002t0002g0247others(4): Show | 10 | NA18950.hp1 NA19007.hp1 NA19054.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-9391C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546738 | ||||||
chr3:138546765
|
T | TA | 91 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.466-9419dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546765 | ||||||
chr3:138546828
|
G | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-9481C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546828 | ||||||
chr3:138546864
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-9517T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546864 | ||||||
chr3:138546897
|
G | A | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466-9550C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138546897 | ||||||
chr3:138547016
|
AAATGAAA others(12): Show |
A | 3 | a0001c0001t0001g0280a0002c0002t0001g0196a0002c0002t0001g0197 | 3 | HG02647.hp2 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.466-9688_466-9670d others(21): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547016 | ||||||
chr3:138547142
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(280): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.466-9795C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547142 | ||||||
chr3:138547146
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(280): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.466-9799T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547146 | ||||||
chr3:138547336
|
T | C | 2 | a0003c0003t0003g0069a0003c0003t0003g0071 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.466-9989A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547336 | ||||||
chr3:138547754
|
G | A | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.466-10407C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547754 | ||||||
chr3:138547793
|
G | A | 91 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.466-10446C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547793 | ||||||
chr3:138547861
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.466-10514A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547861 | ||||||
chr3:138547922
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.466-10575G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138547922 | ||||||
chr3:138548044
|
A | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-10697T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548044 | ||||||
chr3:138548055
|
A | C | 2 | a0003c0003t0003g0114a0003c0003t0003g0115 | 2 | NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.466-10708T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548055 | ||||||
chr3:138548063
|
T | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-10716A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548063 | ||||||
chr3:138548202
|
G | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-10855C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548202 | ||||||
chr3:138548251
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-10904A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548251 | ||||||
chr3:138548388
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-11041G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548388 | ||||||
chr3:138548632
|
C | T | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.466-11285G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548632 | ||||||
chr3:138548695
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.466-11348A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548695 | ||||||
chr3:138548931
|
A | G | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.466-11584T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548931 | ||||||
chr3:138548963
|
T | C | 184 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(181): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.466-11616A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138548963 | ||||||
chr3:138549051
|
G | A | 1 | a0003c0003t0001g0027 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.466-11704C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549051 | ||||||
chr3:138549231
|
T | C | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.466-11884A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549231 | ||||||
chr3:138549303
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.466-11956C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549303 | ||||||
chr3:138549304
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.466-11957G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549304 | ||||||
chr3:138549305
|
A | C | 1 | a0001c0001t0001g0040 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.466-11958T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549305 | ||||||
chr3:138549363
|
C | T | 1 | a0003c0003t0003g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.466-12016G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549363 | ||||||
chr3:138549364
|
G | A | 1 | a0003c0003t0003g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.466-12017C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549364 | ||||||
chr3:138549367
|
T | C | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-12020A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549367 | ||||||
chr3:138549588
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12241G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549588 | ||||||
chr3:138549590
|
C | T | 10 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0138others(7): Show | 10 | HG00544.hp2 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-12243G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549590 | ||||||
chr3:138549649
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12302T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549649 | ||||||
chr3:138549673
|
G | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.466-12326C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549673 | ||||||
chr3:138549696
|
C | T | 28 | a0003c0003t0003g0009a0003c0003t0003g0050a0003c0003t0003g0052others(25): Show | 29 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-12349G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549696 | ||||||
chr3:138549697
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12350C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549697 | ||||||
chr3:138549709
|
C | T | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-12362G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549709 | ||||||
chr3:138549719
|
A | T | 182 | a0001c0004t0004g0215a0001c0004t0004g0216a0001c0004t0006g0029others(179): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.466-12372T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549719 | ||||||
chr3:138549820
|
T | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02083.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.466-12473A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549820 | ||||||
chr3:138549874
|
G | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12527C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549874 | ||||||
chr3:138549949
|
T | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-12602A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138549949 | ||||||
chr3:138550041
|
G | A | 1 | a0003c0003t0003g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-12694C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550041 | ||||||
chr3:138550151
|
C | T | 91 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.466-12804G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550151 | ||||||
chr3:138550161
|
C | A | 5 | a0002c0002t0002g0005a0002c0002t0002g0219a0002c0002t0002g0220others(2): Show | 7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-12814G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550161 | ||||||
chr3:138550390
|
T | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-13043A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550390 | ||||||
chr3:138550485
|
T | A | 1 | a0003c0003t0003g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-13138A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550485 | ||||||
chr3:138550609
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-13262G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138550609 | ||||||
chr3:138551180
|
A | T | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.466-13833T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551180 | ||||||
chr3:138551313
|
G | A | 82 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(79): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.466-13966C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551313 | ||||||
chr3:138551557
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.466-14210G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551557 | ||||||
chr3:138551574
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0154 | 2 | NA18941.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.466-14227G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551574 | ||||||
chr3:138551702
|
C | T | 3 | a0003c0003t0003g0043a0003c0003t0003g0047a0003c0003t0003g0048 | 3 | HG00621.hp1 HG00673.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.466-14355G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551702 | ||||||
chr3:138551758
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.466-14411T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551758 | ||||||
chr3:138551758
|
AT | A | 93 | a0001c0004t0004g0109a0001c0004t0004g0110a0002c0002t0002g0005others(90): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.466-14412delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551758 | ||||||
chr3:138551759
|
T | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.466-14412A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551759 | ||||||
chr3:138551760
|
A | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14413T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551760 | ||||||
chr3:138551760
|
A | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 5 | HG02027.hp2 HG02040.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14413T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551760 | ||||||
chr3:138551761
|
A | T | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-14414T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551761 | ||||||
chr3:138551764
|
T | A | 12 | a0001c0004t0006g0029a0001c0004t0006g0032a0002c0002t0002g0233others(9): Show | 12 | HG00323.hp2 HG00735.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.466-14417A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551764 | ||||||
chr3:138551764
|
T | C | 172 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(169): Show | 192 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.466-14417A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551764 | ||||||
chr3:138551769
|
C | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14422G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551769 | ||||||
chr3:138551796
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-14449A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551796 | ||||||
chr3:138551877
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14530A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551877 | ||||||
chr3:138551985
|
T | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-14638A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138551985 | ||||||
chr3:138552312
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-14965G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552312 | ||||||
chr3:138552357
|
C | A | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.466-15010G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552357 | ||||||
chr3:138552447
|
T | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.466-15100A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552447 | ||||||
chr3:138552483
|
A | T | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.466-15136T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552483 | ||||||
chr3:138552511
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.466-15164G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552511 | ||||||
chr3:138552535
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.466-15188A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552535 | ||||||
chr3:138552608
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-15261G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552608 | ||||||
chr3:138552925
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-15578G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552925 | ||||||
chr3:138552938
|
G | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-15591C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138552938 | ||||||
chr3:138553052
|
A | G | 3 | a0002c0002t0002g0233a0002c0002t0002g0249a0002c0002t0002g0267 | 3 | NA18612.hp2 NA18969.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.466-15705T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553052 | ||||||
chr3:138553053
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.466-15706G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553053 | ||||||
chr3:138553207
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.466-15860G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553207 | ||||||
chr3:138553290
|
T | G | 59 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(56): Show | 69 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.466-15943A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553290 | ||||||
chr3:138553341
|
G | A | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.466-15994C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553341 | ||||||
chr3:138553352
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-16005A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553352 | ||||||
chr3:138553353
|
G | A | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-16006C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553353 | ||||||
chr3:138553379
|
C | A | 1 | a0002c0002t0002g0248 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.466-16032G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553379 | ||||||
chr3:138553487
|
C | CA | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(118): Show | 141 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.466-16141dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553487 | ||||||
chr3:138553544
|
A | AAAG | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-16200_466-1619 others(7): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553544 | ||||||
chr3:138553745
|
C | T | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.466-16398G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553745 | ||||||
chr3:138553783
|
T | A | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.466-16436A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138553783 | ||||||
chr3:138554169
|
C | G | 1 | a0003c0003t0003g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.465+16149G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554169 | ||||||
chr3:138554200
|
G | GA | 13 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0167others(10): Show | 13 | HG00280.hp2 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.465+16117dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554200 | ||||||
chr3:138554200
|
GA | G | 30 | a0001c0001t0001g0013a0001c0001t0001g0123a0001c0001t0001g0134others(27): Show | 33 | HG00738.hp2 HG01123.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.465+16117delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554200 | ||||||
chr3:138554292
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+16026G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554292 | ||||||
chr3:138554523
|
G | A | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+15795C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554523 | ||||||
chr3:138554645
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(201): Show | 231 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.465+15673A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554645 | ||||||
chr3:138554827
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+15491A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554827 | ||||||
chr3:138554872
|
G | C | 2 | a0003c0003t0003g0099a0003c0003t0003g0100 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.465+15446C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554872 | ||||||
chr3:138554935
|
T | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15383A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554935 | ||||||
chr3:138554969
|
T | C | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+15349A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554969 | ||||||
chr3:138554998
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15320A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138554998 | ||||||
chr3:138555060
|
C | T | 1 | a0002c0002t0002g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.465+15258G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555060 | ||||||
chr3:138555156
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15162C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555156 | ||||||
chr3:138555180
|
G | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+15138C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555180 | ||||||
chr3:138555193
|
G | A | 1 | a0003c0003t0003g0071 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.465+15125C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555193 | ||||||
chr3:138555248
|
C | CAAAA | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(93): Show | 109 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.465+15066_465+1506 others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555248 | ||||||
chr3:138555248
|
C | CAAAAA | 44 | a0001c0001t0001g0138a0001c0001t0001g0169a0001c0001t0001g0171others(41): Show | 48 | HG00738.hp2 HG01123.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.465+15065_465+1506 others(9): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555248 | ||||||
chr3:138555248
|
C | CAAAAAA | 57 | a0001c0004t0004g0216a0002c0002t0002g0002a0002c0002t0002g0006others(54): Show | 67 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.465+15064_465+1506 others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555248 | ||||||
chr3:138555375
|
T | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+14943A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555375 | ||||||
chr3:138555673
|
A | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14645T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555673 | ||||||
chr3:138555709
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+14609T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555709 | ||||||
chr3:138555910
|
C | T | 1 | a0003c0003t0001g0060 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.465+14408G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138555910 | ||||||
chr3:138556013
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.465+14305C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556013 | ||||||
chr3:138556043
|
G | C | 1 | a0002c0002t0002g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.465+14275C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556043 | ||||||
chr3:138556069
|
C | T | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.465+14249G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556069 | ||||||
chr3:138556121
|
A | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14197T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556121 | ||||||
chr3:138556137
|
T | C | 1 | a0003c0003t0003g0047 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.465+14181A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556137 | ||||||
chr3:138556288
|
C | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14030G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556288 | ||||||
chr3:138556308
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+14010A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556308 | ||||||
chr3:138556414
|
G | C | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+13904C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556414 | ||||||
chr3:138556527
|
C | CA | 17 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0060others(14): Show | 17 | HG00621.hp1 HG00639.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.465+13790dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556527 | ||||||
chr3:138556527
|
CA | C | 94 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0171others(91): Show | 108 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.465+13790delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556527 | ||||||
chr3:138556527
|
CAA | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+13789_465+1379 others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556527 | ||||||
chr3:138556584
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13734C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556584 | ||||||
chr3:138556617
|
C | T | 2 | a0002c0002t0002g0238a0004c0006t0005g0028 | 2 | HG06807.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.465+13701G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556617 | ||||||
chr3:138556635
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13683C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556635 | ||||||
chr3:138556649
|
G | A | 1 | a0003c0003t0003g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.465+13669C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556649 | ||||||
chr3:138556717
|
C | G | 4 | a0001c0004t0004g0215a0001c0004t0004g0216a0006c0010t0004g0023others(1): Show | 4 | HG01243.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+13601G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556717 | ||||||
chr3:138556728
|
G | A | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.465+13590C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556728 | ||||||
chr3:138556776
|
G | T | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+13542C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556776 | ||||||
chr3:138556780
|
T | C | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.465+13538A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556780 | ||||||
chr3:138556797
|
G | A | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+13521C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556797 | ||||||
chr3:138556865
|
G | A | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+13453C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556865 | ||||||
chr3:138556969
|
T | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.465+13349A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556969 | ||||||
chr3:138556985
|
G | A | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.465+13333C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138556985 | ||||||
chr3:138557036
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13282T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557036 | ||||||
chr3:138557043
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+13275G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557043 | ||||||
chr3:138557049
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+13269A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557049 | ||||||
chr3:138557100
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+13218G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557100 | ||||||
chr3:138557120
|
T | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13198A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557120 | ||||||
chr3:138557141
|
A | G | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465+13177T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557141 | ||||||
chr3:138557201
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13117T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557201 | ||||||
chr3:138557209
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+13109C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557209 | ||||||
chr3:138557291
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.465+13027G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557291 | ||||||
chr3:138557313
|
TACAA | T | 9 | a0001c0004t0006g0029a0001c0004t0006g0032a0003c0003t0003g0050others(6): Show | 9 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+13001_465+1300 others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557313 | ||||||
chr3:138557354
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+12964A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557354 | ||||||
chr3:138557428
|
G | T | 2 | a0003c0003t0001g0067a0003c0003t0001g0192 | 2 | HG01071.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.465+12890C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557428 | ||||||
chr3:138557435
|
T | C | 1 | a0002c0002t0002g0231 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.465+12883A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557435 | ||||||
chr3:138557440
|
G | T | 1 | a0003c0003t0003g0042 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.465+12878C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557440 | ||||||
chr3:138557576
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+12742A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557576 | ||||||
chr3:138557644
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.465+12674A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557644 | ||||||
chr3:138557669
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.465+12649T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557669 | ||||||
chr3:138557699
|
T | C | 77 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(74): Show | 90 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.465+12619A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557699 | ||||||
chr3:138557712
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.465+12606T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557712 | ||||||
chr3:138557843
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.465+12475C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557843 | ||||||
chr3:138557873
|
T | C | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+12445A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557873 | ||||||
chr3:138557970
|
A | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+12348T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138557970 | ||||||
chr3:138558018
|
T | C | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.465+12300A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558018 | ||||||
chr3:138558106
|
T | C | 1 | a0002c0002t0002g0259 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.465+12212A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558106 | ||||||
chr3:138558124
|
C | T | 1 | a0002c0002t0002g0232 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.465+12194G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558124 | ||||||
chr3:138558139
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.465+12179G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558139 | ||||||
chr3:138558167
|
C | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+12151G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558167 | ||||||
chr3:138558274
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(104): Show | 120 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.465+12044G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558274 | ||||||
chr3:138558275
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.465+12043T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558275 | ||||||
chr3:138558329
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+11989G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558329 | ||||||
chr3:138558360
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+11958C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558360 | ||||||
chr3:138558388
|
T | C | 1 | a0003c0003t0003g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.465+11930A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558388 | ||||||
chr3:138558510
|
T | C | 3 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028 | 3 | HG02615.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+11808A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558510 | ||||||
chr3:138558608
|
T | C | 1 | a0002c0002t0001g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.465+11710A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558608 | ||||||
chr3:138558848
|
C | T | 1 | a0001c0004t0004g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.465+11470G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138558848 | ||||||
chr3:138559069
|
T | C | 1 | a0002c0002t0001g0210 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.465+11249A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559069 | ||||||
chr3:138559086
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.465+11232G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559086 | ||||||
chr3:138559159
|
C | T | 12 | a0003c0003t0001g0027a0003c0003t0003g0009a0003c0003t0003g0061others(9): Show | 13 | HG00140.hp1 HG00735.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+11159G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559159 | ||||||
chr3:138559202
|
G | A | 1 | a0002c0002t0002g0261 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.465+11116C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559202 | ||||||
chr3:138559364
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(194): Show | 224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.465+10954C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559364 | ||||||
chr3:138559377
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+10941A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559377 | ||||||
chr3:138559378
|
G | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+10940C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559378 | ||||||
chr3:138559413
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+10905C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559413 | ||||||
chr3:138559487
|
C | T | 11 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(8): Show | 11 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.465+10831G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559487 | ||||||
chr3:138559632
|
G | A | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+10686C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559632 | ||||||
chr3:138559656
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.465+10662G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138559656 | ||||||
chr3:138560112
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+10206G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560112 | ||||||
chr3:138560143
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | NA18945.hp1 NA18975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.465+10175G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560143 | ||||||
chr3:138560218
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02083.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.465+10100C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560218 | ||||||
chr3:138560338
|
T | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9980A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560338 | ||||||
chr3:138560373
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9945C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560373 | ||||||
chr3:138560473
|
G | GT | 14 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0135others(11): Show | 14 | HG01099.hp2 HG01243.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.465+9844dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560473 | ||||||
chr3:138560473
|
G | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465+9845C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560473 | ||||||
chr3:138560567
|
AGGTCTG | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9745_465+9750d others(8): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560567 | ||||||
chr3:138560708
|
G | A | 91 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.465+9610C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560708 | ||||||
chr3:138560944
|
G | A | 2 | a0003c0003t0003g0076a0003c0003t0003g0091 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.465+9374C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560944 | ||||||
chr3:138560960
|
G | T | 1 | a0001c0001t0001g0134 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.465+9358C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560960 | ||||||
chr3:138560973
|
G | A | 1 | a0002c0002t0001g0207 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.465+9345C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560973 | ||||||
chr3:138560986
|
G | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+9332C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138560986 | ||||||
chr3:138561015
|
C | G | 1 | a0002c0002t0001g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.465+9303G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561015 | ||||||
chr3:138561032
|
G | A | 8 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(5): Show | 8 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+9286C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561032 | ||||||
chr3:138561046
|
G | A | 1 | a0003c0003t0003g0097 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.465+9272C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561046 | ||||||
chr3:138561136
|
G | A | 1 | a0002c0002t0001g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.465+9182C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561136 | ||||||
chr3:138561171
|
G | A | 1 | a0002c0002t0002g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.465+9147C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561171 | ||||||
chr3:138561376
|
C | T | 1 | a0002c0002t0002g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.465+8942G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561376 | ||||||
chr3:138561401
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.465+8917C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561401 | ||||||
chr3:138561826
|
A | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.465+8492T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561826 | ||||||
chr3:138561852
|
G | A | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+8466C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561852 | ||||||
chr3:138561896
|
C | T | 1 | a0003c0003t0003g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.465+8422G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561896 | ||||||
chr3:138561968
|
A | G | 1 | a0003c0003t0003g0101 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.465+8350T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138561968 | ||||||
chr3:138562002
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+8316C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562002 | ||||||
chr3:138562022
|
CA | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(184): Show | 210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.465+8295delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562022 | ||||||
chr3:138562074
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.465+8244G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562074 | ||||||
chr3:138562075
|
C | T | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+8243G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562075 | ||||||
chr3:138562163
|
T | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+8155A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562163 | ||||||
chr3:138562242
|
A | C | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+8076T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562242 | ||||||
chr3:138562321
|
T | C | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+7997A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562321 | ||||||
chr3:138562326
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.465+7992C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562326 | ||||||
chr3:138562332
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+7986G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562332 | ||||||
chr3:138562344
|
G | GA | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+7973dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562344 | ||||||
chr3:138562361
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+7957G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562361 | ||||||
chr3:138562434
|
A | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.465+7884T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562434 | ||||||
chr3:138562449
|
C | A | 4 | a0002c0002t0002g0237a0002c0002t0002g0257a0002c0002t0002g0258others(1): Show | 4 | HG00408.hp2 HG02074.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+7869G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562449 | ||||||
chr3:138562497
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.465+7821G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562497 | ||||||
chr3:138562522
|
C | T | 1 | a0002c0002t0002g0225 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.465+7796G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562522 | ||||||
chr3:138562742
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.465+7576G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562742 | ||||||
chr3:138562933
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.465+7385A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138562933 | ||||||
chr3:138563029
|
CA | C | 6 | a0001c0001t0001g0218a0001c0004t0006g0029a0001c0004t0006g0032others(3): Show | 6 | HG00280.hp1 HG00735.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+7288delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563029 | ||||||
chr3:138563062
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.465+7256A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563062 | ||||||
chr3:138563080
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.465+7238T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563080 | ||||||
chr3:138563135
|
G | GCAA | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+7180_465+7182d others(5): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563135 | ||||||
chr3:138563254
|
G | A | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+7064C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563254 | ||||||
chr3:138563350
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.465+6968G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563350 | ||||||
chr3:138563601
|
G | A | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6717C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563601 | ||||||
chr3:138563634
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+6684C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563634 | ||||||
chr3:138563649
|
T | C | 3 | a0003c0003t0003g0098a0003c0003t0003g0099a0003c0003t0003g0100 | 3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.465+6669A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563649 | ||||||
chr3:138563655
|
C | A | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6663G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563655 | ||||||
chr3:138563726
|
G | A | 1 | a0002c0002t0002g0270 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.465+6592C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563726 | ||||||
chr3:138563764
|
A | AC | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+6553dupG | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563764 | ||||||
chr3:138563764
|
A | G | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+6554T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563764 | ||||||
chr3:138563778
|
T | C | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6540A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563778 | ||||||
chr3:138563789
|
A | G | 1 | a0002c0002t0002g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.465+6529T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563789 | ||||||
chr3:138563809
|
A | T | 15 | a0002c0002t0002g0006a0002c0002t0002g0020a0002c0002t0002g0022others(12): Show | 19 | HG01346.hp1 HG01884.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.465+6509T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563809 | ||||||
chr3:138563857
|
T | C | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+6461A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138563857 | ||||||
chr3:138564104
|
T | C | 1 | a0002c0002t0001g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.465+6214A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564104 | ||||||
chr3:138564310
|
C | T | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.465+6008G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564310 | ||||||
chr3:138564428
|
C | G | 1 | a0002c0002t0002g0262 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.465+5890G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564428 | ||||||
chr3:138564501
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(97): Show | 113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.465+5817C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564501 | ||||||
chr3:138564617
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+5701A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564617 | ||||||
chr3:138564687
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+5631G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564687 | ||||||
chr3:138564824
|
A | C | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+5494T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138564824 | ||||||
chr3:138565149
|
G | A | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+5169C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565149 | ||||||
chr3:138565208
|
A | C | 1 | a0002c0002t0002g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.465+5110T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565208 | ||||||
chr3:138565220
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.465+5098A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565220 | ||||||
chr3:138565266
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+5052A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565266 | ||||||
chr3:138565518
|
C | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+4800G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565518 | ||||||
chr3:138565528
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+4790C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565528 | ||||||
chr3:138565555
|
C | T | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+4763G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565555 | ||||||
chr3:138565670
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.465+4648G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565670 | ||||||
chr3:138565721
|
C | G | 1 | a0002c0002t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.465+4597G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565721 | ||||||
chr3:138565733
|
C | T | 2 | a0002c0002t0002g0261a0002c0002t0002g0265 | 2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.465+4585G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565733 | ||||||
chr3:138565749
|
G | A | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+4569C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565749 | ||||||
chr3:138565874
|
A | G | 1 | a0002c0002t0002g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.465+4444T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565874 | ||||||
chr3:138565921
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.465+4397G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565921 | ||||||
chr3:138565922
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.465+4396G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138565922 | ||||||
chr3:138566060
|
C | T | 7 | a0002c0002t0002g0005a0002c0002t0002g0036a0002c0002t0002g0037others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.465+4258G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566060 | ||||||
chr3:138566153
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.465+4165C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566153 | ||||||
chr3:138566184
|
C | T | 1 | a0001c0004t0004g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.465+4134G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566184 | ||||||
chr3:138566220
|
T | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+4098A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566220 | ||||||
chr3:138566278
|
A | G | 1 | a0001c0004t0006g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.465+4040T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566278 | ||||||
chr3:138566373
|
T | C | 1 | a0003c0003t0003g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.465+3945A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566373 | ||||||
chr3:138566379
|
C | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+3939G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566379 | ||||||
chr3:138566379
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+3939G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566379 | ||||||
chr3:138566493
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+3825G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566493 | ||||||
chr3:138566601
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+3717C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566601 | ||||||
chr3:138566681
|
G | A | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.465+3637C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566681 | ||||||
chr3:138566803
|
G | GTA | 65 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(62): Show | 76 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.465+3513_465+3514d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566803 | ||||||
chr3:138566803
|
G | GTATA | 2 | a0002c0002t0002g0021a0002c0002t0002g0260 | 3 | HG00544.hp1 NA19012.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.465+3511_465+3514d others(6): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566803 | ||||||
chr3:138566803
|
GTA | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+3513_465+3514d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566803 | ||||||
chr3:138566815
|
A | C | 1 | a0003c0003t0003g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.465+3503T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566815 | ||||||
chr3:138566820
|
A | T | 14 | a0002c0002t0002g0006a0002c0002t0002g0020a0003c0003t0003g0034others(11): Show | 17 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.465+3498T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138566820 | ||||||
chr3:138567060
|
A | T | 2 | a0003c0003t0003g0050a0003c0003t0003g0081 | 2 | NA18986.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.465+3258T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567060 | ||||||
chr3:138567199
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.465+3119A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567199 | ||||||
chr3:138567338
|
T | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+2980A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567338 | ||||||
chr3:138567576
|
G | A | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.465+2742C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567576 | ||||||
chr3:138567619
|
T | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465+2699A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567619 | ||||||
chr3:138567633
|
C | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.465+2685G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567633 | ||||||
chr3:138567867
|
T | C | 1 | a0003c0003t0003g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.465+2451A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567867 | ||||||
chr3:138567888
|
G | A | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.465+2430C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567888 | ||||||
chr3:138567983
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+2335C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567983 | ||||||
chr3:138567985
|
C | T | 1 | a0002c0002t0002g0239 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.465+2333G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567985 | ||||||
chr3:138567999
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.465+2319A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138567999 | ||||||
chr3:138568058
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+2260G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568058 | ||||||
chr3:138568230
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.465+2088G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568230 | ||||||
chr3:138568427
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.465+1891A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568427 | ||||||
chr3:138568703
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG00408.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.465+1615C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568703 | ||||||
chr3:138568836
|
G | A | 5 | a0001c0004t0004g0109a0001c0004t0004g0110a0001c0004t0004g0215others(2): Show | 5 | HG02258.hp1 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1482C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568836 | ||||||
chr3:138568843
|
G | A | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+1475C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568843 | ||||||
chr3:138568889
|
G | A | 1 | a0003c0003t0003g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.465+1429C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568889 | ||||||
chr3:138568994
|
C | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(198): Show | 228 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.465+1324G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568994 | ||||||
chr3:138568994
|
C | CA | 6 | a0003c0003t0003g0003a0003c0003t0003g0077a0003c0003t0003g0097others(3): Show | 8 | HG01243.hp2 HG02559.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.465+1323dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568994 | ||||||
chr3:138568995
|
A | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(188): Show | 218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.465+1323T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568995 | ||||||
chr3:138568996
|
A | C | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.465+1322T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138568996 | ||||||
chr3:138569000
|
A | C | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+1318T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569000 | ||||||
chr3:138569009
|
A | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1309T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569009 | ||||||
chr3:138569101
|
A | C | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.465+1217T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569101 | ||||||
chr3:138569171
|
C | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.465+1147G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569171 | ||||||
chr3:138569279
|
C | G | 1 | a0002c0002t0002g0238 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.465+1039G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569279 | ||||||
chr3:138569282
|
G | T | 1 | a0002c0002t0001g0201 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.465+1036C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569282 | ||||||
chr3:138569283
|
C | T | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+1035G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569283 | ||||||
chr3:138569482
|
A | C | 2 | a0001c0001t0001g0112a0001c0011t0001g0111 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.465+836T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569482 | ||||||
chr3:138569530
|
A | C | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+788T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569530 | ||||||
chr3:138569633
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+685G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569633 | ||||||
chr3:138569729
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.465+589C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569729 | ||||||
chr3:138569737
|
A | G | 1 | a0002c0002t0002g0237 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.465+581T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569737 | ||||||
chr3:138569758
|
C | T | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.465+560G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569758 | ||||||
chr3:138569962
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+356C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569962 | ||||||
chr3:138569980
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.465+338G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138569980 | ||||||
chr3:138570224
|
A | G | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+94T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 6/17 | chr3 | 138570224 | ||||||
chr3:138570574
|
T | C | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.285-76A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 5/17 | chr3 | 138570574 | ||||||
chr3:138570778
|
T | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(277): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.284+256A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 5/17 | chr3 | 138570778 | ||||||
chr3:138570787
|
C | G | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.284+247G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 5/17 | chr3 | 138570787 | ||||||
chr3:138571189
|
A | AAAAATAA others(1801): Show |
2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.161-33_161-32insGT others(1806): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 4/17 | chr3 | 138571189 | ||||||
chr3:138571220
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.160+46T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 4/17 | chr3 | 138571220 | ||||||
chr3:138571594
|
G | C | 1 | a0003c0003t0003g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.70-238C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571594 | ||||||
chr3:138571647
|
A | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70-291T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571647 | ||||||
chr3:138571740
|
T | TAAAGA | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-389_70-385dupTC others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571740 | ||||||
chr3:138571766
|
C | A | 1 | a0002c0002t0001g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.70-410G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571766 | ||||||
chr3:138571820
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.70-464G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571820 | ||||||
chr3:138571836
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.70-480G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571836 | ||||||
chr3:138571905
|
A | G | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.70-549T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571905 | ||||||
chr3:138571935
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.70-579G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138571935 | ||||||
chr3:138572069
|
C | CA | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.70-714_70-713insT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572069 | ||||||
chr3:138572200
|
G | A | 2 | a0002c0002t0002g0261a0002c0002t0002g0265 | 2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.69+659C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572200 | ||||||
chr3:138572216
|
G | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.69+643C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572216 | ||||||
chr3:138572310
|
C | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.69+549G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572310 | ||||||
chr3:138572369
|
C | G | 1 | a0003c0003t0003g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.69+490G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572369 | ||||||
chr3:138572370
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG00673.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.69+489C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572370 | ||||||
chr3:138572392
|
A | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.69+467T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572392 | ||||||
chr3:138572395
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.69+464A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572395 | ||||||
chr3:138572515
|
A | G | 1 | a0004c0006t0005g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.69+344T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572515 | ||||||
chr3:138572531
|
C | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.69+328G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572531 | ||||||
chr3:138572664
|
G | A | 3 | a0002c0002t0002g0262a0002c0002t0002g0263a0002c0002t0002g0264 | 3 | NA18994.hp2 NA19062.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.69+195C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572664 | ||||||
chr3:138572690
|
T | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0127a0001c0001t0001g0179 | 4 | HG01256.hp2 HG01258.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+169A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572690 | ||||||
chr3:138572706
|
T | C | 1 | a0003c0003t0003g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.69+153A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572706 | ||||||
chr3:138572727
|
T | C | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(66): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.69+132A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 3/17 | chr3 | 138572727 | ||||||
chr3:138572976
|
T | C | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-44A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138572976 | ||||||
chr3:138573091
|
G | C | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-159C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573091 | ||||||
chr3:138573142
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-5-210T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573142 | ||||||
chr3:138573205
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-273G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573205 | ||||||
chr3:138573207
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-275G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573207 | ||||||
chr3:138573309
|
A | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-377T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573309 | ||||||
chr3:138573380
|
T | TA | 16 | a0001c0001t0001g0180a0002c0002t0002g0033a0003c0003t0003g0050others(13): Show | 16 | HG01243.hp2 HG01255.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-449dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573380 | ||||||
chr3:138573420
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-5-488G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573420 | ||||||
chr3:138573561
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-629A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138573561 | ||||||
chr3:138574025
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-5-1093C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574025 | ||||||
chr3:138574118
|
C | T | 1 | a0003c0003t0003g0034 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-5-1186G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574118 | ||||||
chr3:138574122
|
C | T | 1 | a0002c0002t0002g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-5-1190G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574122 | ||||||
chr3:138574141
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-1209A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574141 | ||||||
chr3:138574168
|
G | A | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(66): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-5-1236C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574168 | ||||||
chr3:138574194
|
A | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0129a0001c0001t0001g0188 | 5 | HG01123.hp1 HG01257.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-1262T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574194 | ||||||
chr3:138574200
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(97): Show | 113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-5-1268A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574200 | ||||||
chr3:138574246
|
C | T | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-1314G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574246 | ||||||
chr3:138574247
|
G | A | 3 | a0002c0002t0002g0229a0002c0002t0002g0230a0002c0002t0002g0231 | 3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-5-1315C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574247 | ||||||
chr3:138574411
|
G | A | 1 | a0003c0003t0003g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-1479C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574411 | ||||||
chr3:138574431
|
C | T | 5 | a0002c0002t0002g0005a0002c0002t0002g0219a0002c0002t0002g0220others(2): Show | 7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-1499G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574431 | ||||||
chr3:138574449
|
T | C | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(66): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-5-1517A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574449 | ||||||
chr3:138574518
|
T | C | 1 | a0003c0003t0003g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-5-1586A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574518 | ||||||
chr3:138574558
|
T | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-1626A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574558 | ||||||
chr3:138574564
|
T | C | 1 | a0002c0002t0002g0265 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-5-1632A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574564 | ||||||
chr3:138574656
|
C | T | 58 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(55): Show | 68 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-5-1724G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574656 | ||||||
chr3:138574660
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-1728C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574660 | ||||||
chr3:138574895
|
A | G | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-1963T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574895 | ||||||
chr3:138574898
|
G | A | 3 | a0003c0005t0003g0058a0003c0005t0003g0088a0003c0005t0003g0089 | 3 | HG02280.hp1 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-5-1966C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574898 | ||||||
chr3:138574987
|
A | C | 1 | a0003c0003t0003g0043 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-5-2055T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138574987 | ||||||
chr3:138575080
|
C | G | 1 | a0003c0005t0003g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5-2148G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575080 | ||||||
chr3:138575090
|
T | C | 1 | a0002c0002t0002g0006 | 3 | HG02735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-5-2158A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575090 | ||||||
chr3:138575107
|
G | T | 1 | a0003c0003t0003g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-5-2175C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575107 | ||||||
chr3:138575264
|
G | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2332C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575264 | ||||||
chr3:138575304
|
A | T | 13 | a0001c0001t0001g0112a0001c0001t0001g0275a0001c0001t0001g0276others(10): Show | 13 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5-2372T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575304 | ||||||
chr3:138575383
|
C | T | 2 | a0003c0003t0003g0054a0006c0010t0004g0023 | 2 | HG01243.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-5-2451G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575383 | ||||||
chr3:138575393
|
A | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-2461T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575393 | ||||||
chr3:138575471
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(201): Show | 231 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.-5-2539G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575471 | ||||||
chr3:138575473
|
G | C | 2 | a0003c0003t0003g0094a0003c0003t0003g0095 | 2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-5-2541C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575473 | ||||||
chr3:138575474
|
T | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(201): Show | 231 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.-5-2542A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575474 | ||||||
chr3:138575494
|
T | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(278): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.-5-2562A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575494 | ||||||
chr3:138575499
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2567C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575499 | ||||||
chr3:138575513
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2581G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575513 | ||||||
chr3:138575529
|
A | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2597T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575529 | ||||||
chr3:138575565
|
G | C | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-2633C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575565 | ||||||
chr3:138575620
|
G | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0127 | 3 | HG01256.hp2 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-5-2688C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575620 | ||||||
chr3:138575944
|
G | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-3012C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575944 | ||||||
chr3:138575975
|
C | G | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-3043G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575975 | ||||||
chr3:138575975
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-3043G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575975 | ||||||
chr3:138575976
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-3044T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138575976 | ||||||
chr3:138576216
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-3284C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576216 | ||||||
chr3:138576287
|
G | C | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5-3355C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576287 | ||||||
chr3:138576332
|
G | A | 2 | a0002c0002t0002g0021a0002c0002t0002g0235 | 3 | HG00544.hp1 HG00558.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-5-3400C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576332 | ||||||
chr3:138576416
|
C | T | 1 | a0004c0006t0005g0030 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-5-3484G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576416 | ||||||
chr3:138576419
|
G | A | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-3487C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576419 | ||||||
chr3:138576501
|
T | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-3569A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576501 | ||||||
chr3:138576684
|
T | C | 1 | a0003c0003t0003g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-5-3752A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576684 | ||||||
chr3:138576711
|
T | A | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-3779A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576711 | ||||||
chr3:138576770
|
G | A | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-3838C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576770 | ||||||
chr3:138576773
|
A | C | 1 | a0003c0003t0003g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-3841T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576773 | ||||||
chr3:138576808
|
C | G | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-3876G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576808 | ||||||
chr3:138576852
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-5-3920T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138576852 | ||||||
chr3:138577036
|
T | A | 1 | a0002c0002t0001g0211 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-5-4104A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577036 | ||||||
chr3:138577167
|
G | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(275): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-5-4235C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577167 | ||||||
chr3:138577193
|
C | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-4261G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577193 | ||||||
chr3:138577194
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(194): Show | 224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-5-4262C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577194 | ||||||
chr3:138577201
|
G | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-5-4269C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577201 | ||||||
chr3:138577208
|
T | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-4276A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577208 | ||||||
chr3:138577233
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(201): Show | 231 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.-5-4301C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577233 | ||||||
chr3:138577357
|
T | TA | 2 | a0002c0002t0002g0007a0002c0002t0002g0272 | 4 | HG02040.hp1 NA18942.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-4426dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577357 | ||||||
chr3:138577419
|
C | A | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-4487G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577419 | ||||||
chr3:138577421
|
G | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG00408.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-5-4489C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577421 | ||||||
chr3:138577580
|
G | A | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-4648C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577580 | ||||||
chr3:138577596
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-5-4664G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577596 | ||||||
chr3:138577664
|
T | A | 26 | a0001c0004t0006g0029a0001c0004t0006g0032a0002c0002t0001g0018others(23): Show | 28 | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5-4732A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577664 | ||||||
chr3:138577778
|
T | A | 1 | a0002c0002t0002g0273 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-5-4846A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138577778 | ||||||
chr3:138578037
|
C | T | 3 | a0003c0003t0003g0098a0003c0003t0003g0099a0003c0003t0003g0100 | 3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-5-5105G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578037 | ||||||
chr3:138578046
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG01175.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-5-5114T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578046 | ||||||
chr3:138578126
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(97): Show | 113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-5-5194G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578126 | ||||||
chr3:138578272
|
C | T | 3 | a0004c0006t0005g0028a0004c0006t0005g0030a0004c0006t0005g0031 | 3 | HG00735.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5-5340G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578272 | ||||||
chr3:138578564
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-5632G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578564 | ||||||
chr3:138578642
|
A | T | 59 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(56): Show | 69 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-5-5710T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578642 | ||||||
chr3:138578718
|
C | A | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-5786G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578718 | ||||||
chr3:138578719
|
A | C | 2 | a0001c0004t0004g0109a0001c0004t0004g0110 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-5-5787T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578719 | ||||||
chr3:138578844
|
G | A | 1 | a0003c0003t0003g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5-5912C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578844 | ||||||
chr3:138578899
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-5-5967G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138578899 | ||||||
chr3:138579089
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-6157C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579089 | ||||||
chr3:138579140
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-5-6208A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579140 | ||||||
chr3:138579167
|
C | A | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-6235G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579167 | ||||||
chr3:138579235
|
C | T | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(66): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-5-6303G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579235 | ||||||
chr3:138579396
|
C | T | 2 | a0001c0004t0004g0215a0001c0004t0004g0216 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-6464G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579396 | ||||||
chr3:138579513
|
C | T | 1 | a0003c0003t0003g0042 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-5-6581G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579513 | ||||||
chr3:138579535
|
A | G | 1 | a0002c0002t0002g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-5-6603T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579535 | ||||||
chr3:138579741
|
T | C | 3 | a0003c0003t0003g0098a0003c0003t0003g0099a0003c0003t0003g0100 | 3 | HG01243.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-5-6809A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579741 | ||||||
chr3:138579771
|
C | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-6839G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579771 | ||||||
chr3:138579847
|
T | C | 1 | a0003c0003t0003g0049 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-5-6915A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138579847 | ||||||
chr3:138580195
|
T | C | 1 | a0003c0003t0003g0034 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-5-7263A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580195 | ||||||
chr3:138580267
|
C | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-7335G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580267 | ||||||
chr3:138580382
|
A | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-5-7450T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580382 | ||||||
chr3:138580413
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-7481G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580413 | ||||||
chr3:138580421
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-7489G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580421 | ||||||
chr3:138580450
|
T | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-5-7518A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580450 | ||||||
chr3:138580725
|
T | C | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-7793A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580725 | ||||||
chr3:138580795
|
C | G | 7 | a0002c0002t0002g0005a0002c0002t0002g0036a0002c0002t0002g0037others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-7863G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580795 | ||||||
chr3:138580881
|
T | C | 1 | a0001c0001t0001g0017 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-5-7949A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580881 | ||||||
chr3:138580914
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-7982A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580914 | ||||||
chr3:138580990
|
A | C | 1 | a0003c0003t0003g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-5-8058T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138580990 | ||||||
chr3:138581001
|
C | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5-8069G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581001 | ||||||
chr3:138581154
|
G | A | 2 | a0003c0003t0003g0092a0006c0010t0004g0023 | 2 | HG01243.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-5-8222C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581154 | ||||||
chr3:138581215
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(194): Show | 224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-5-8283C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581215 | ||||||
chr3:138581239
|
G | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-5-8307C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581239 | ||||||
chr3:138581281
|
CA | C | 7 | a0001c0004t0006g0029a0001c0004t0006g0032a0002c0002t0002g0235others(4): Show | 7 | HG00558.hp2 HG00735.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-8350delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581281 | ||||||
chr3:138581301
|
G | A | 1 | a0002c0002t0002g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5-8369C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581301 | ||||||
chr3:138581395
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-8463T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581395 | ||||||
chr3:138581489
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-8557A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581489 | ||||||
chr3:138581576
|
G | C | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-8644C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581576 | ||||||
chr3:138581628
|
G | A | 1 | a0002c0002t0002g0231 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-5-8696C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581628 | ||||||
chr3:138581694
|
C | CA | 23 | a0001c0001t0001g0275a0002c0002t0001g0018a0002c0002t0001g0019others(20): Show | 25 | HG00735.hp1 HG01123.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.-5-8763dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581694 | ||||||
chr3:138581694
|
CA | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(161): Show | 189 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.-5-8763delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581694 | ||||||
chr3:138581694
|
CAA | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0004t0004g0215others(4): Show | 7 | HG03195.hp2 HG03516.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-8764_-5-8763del others(2): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581694 | ||||||
chr3:138581719
|
T | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-5-8787A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581719 | ||||||
chr3:138581827
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-8895A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581827 | ||||||
chr3:138581893
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-5-8961T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581893 | ||||||
chr3:138581927
|
A | C | 95 | a0001c0004t0004g0215a0001c0004t0004g0216a0002c0002t0001g0018others(92): Show | 109 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5-8995T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581927 | ||||||
chr3:138581993
|
A | C | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-5-9061T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138581993 | ||||||
chr3:138582011
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-5-9079C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582011 | ||||||
chr3:138582132
|
C | T | 2 | a0002c0002t0001g0198a0002c0002t0001g0199 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-5-9200G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582132 | ||||||
chr3:138582193
|
T | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-9261A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582193 | ||||||
chr3:138582365
|
G | A | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-5-9433C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582365 | ||||||
chr3:138582409
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9445G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582409 | ||||||
chr3:138582472
|
A | AAAAAATT | 91 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.-6+9375_-6+9381dup others(7): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582472 | ||||||
chr3:138582494
|
A | G | 2 | a0002c0002t0001g0196a0002c0002t0001g0197 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-6+9360T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582494 | ||||||
chr3:138582599
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9255T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582599 | ||||||
chr3:138582770
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9084T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582770 | ||||||
chr3:138582773
|
A | AAAAT | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+9077_-6+9080dup others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582773 | ||||||
chr3:138582906
|
A | T | 1 | a0001c0001t0001g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-6+8948T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582906 | ||||||
chr3:138582912
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6+8942G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582912 | ||||||
chr3:138582987
|
A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG00639.hp2 HG02735.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+8867T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138582987 | ||||||
chr3:138583179
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-6+8675T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583179 | ||||||
chr3:138583349
|
T | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+8505A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583349 | ||||||
chr3:138583641
|
GT | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+8212delA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583641 | ||||||
chr3:138583692
|
AG | A | 90 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(87): Show | 104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.-6+8161delC | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583692 | ||||||
chr3:138583694
|
G | C | 90 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(87): Show | 104 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.-6+8160C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583694 | ||||||
chr3:138583737
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+8117T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583737 | ||||||
chr3:138583798
|
C | T | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-6+8056G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583798 | ||||||
chr3:138583973
|
GAAC | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+7878_-6+7880del others(3): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138583973 | ||||||
chr3:138584236
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-6+7618A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584236 | ||||||
chr3:138584281
|
G | C | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-6+7573C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584281 | ||||||
chr3:138584333
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(100): Show | 116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-6+7521G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584333 | ||||||
chr3:138584456
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-6+7398G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584456 | ||||||
chr3:138584461
|
C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(112): Show | 129 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-6+7392dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584461 | ||||||
chr3:138584478
|
A | G | 3 | a0002c0002t0002g0006a0002c0002t0002g0020a0002c0002t0002g0232 | 6 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+7376T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584478 | ||||||
chr3:138584529
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+7325A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584529 | ||||||
chr3:138584722
|
A | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+7132T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584722 | ||||||
chr3:138584782
|
G | T | 3 | a0002c0002t0002g0229a0002c0002t0002g0230a0002c0002t0002g0231 | 3 | NA18965.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-6+7072C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584782 | ||||||
chr3:138584907
|
A | C | 5 | a0002c0002t0002g0223a0002c0002t0002g0225a0002c0002t0002g0226others(2): Show | 5 | HG02071.hp1 NA18747.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+6947T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138584907 | ||||||
chr3:138585122
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-6+6732G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585122 | ||||||
chr3:138585256
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-6+6598T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585256 | ||||||
chr3:138585356
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(100): Show | 116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-6+6498T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585356 | ||||||
chr3:138585397
|
C | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-6+6457G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585397 | ||||||
chr3:138585458
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-6+6396A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585458 | ||||||
chr3:138585830
|
T | C | 4 | a0003c0003t0003g0097a0003c0003t0003g0098a0003c0003t0003g0099others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+6024A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585830 | ||||||
chr3:138585833
|
A | G | 2 | a0002c0002t0002g0036a0002c0002t0002g0037 | 2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-6+6021T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138585833 | ||||||
chr3:138586005
|
C | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+5849G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586005 | ||||||
chr3:138586260
|
C | T | 24 | a0001c0004t0006g0029a0001c0004t0006g0032a0003c0003t0003g0012others(21): Show | 25 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6+5594G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586260 | ||||||
chr3:138586345
|
A | T | 1 | a0002c0002t0002g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-6+5509T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586345 | ||||||
chr3:138586511
|
T | A | 10 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6+5343A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586511 | ||||||
chr3:138586511
|
T | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(90): Show | 106 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-6+5343A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586511 | ||||||
chr3:138586560
|
T | C | 20 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(17): Show | 22 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.-6+5294A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586560 | ||||||
chr3:138586650
|
C | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+5204G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586650 | ||||||
chr3:138586675
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-6+5179C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586675 | ||||||
chr3:138586905
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+4949T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138586905 | ||||||
chr3:138587059
|
C | G | 3 | a0002c0002t0001g0018a0002c0002t0001g0194a0002c0002t0001g0195 | 4 | HG02257.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+4795G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587059 | ||||||
chr3:138587290
|
TA | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-6+4563delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587290 | ||||||
chr3:138587321
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+4533A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587321 | ||||||
chr3:138587471
|
T | A | 1 | a0007c0009t0004g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6+4383A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587471 | ||||||
chr3:138587474
|
A | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(199): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-6+4380T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587474 | ||||||
chr3:138587524
|
T | C | 10 | a0003c0003t0003g0012a0003c0003t0003g0039a0003c0003t0003g0101others(7): Show | 11 | HG01167.hp1 HG01169.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6+4330A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587524 | ||||||
chr3:138587578
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+4276T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587578 | ||||||
chr3:138587620
|
C | CAAAAAAA others(3): Show |
118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-6+4233_-6+4234ins others(10): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587620 | ||||||
chr3:138587620
|
C | CAAAAAAA others(4): Show |
84 | a0001c0001t0001g0191a0001c0004t0006g0029a0001c0004t0006g0032others(81): Show | 96 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-6+4233_-6+4234ins others(11): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138587620 | ||||||
chr3:138588016
|
A | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+3838T>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588016 | ||||||
chr3:138588056
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3798C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588056 | ||||||
chr3:138588192
|
C | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+3662G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588192 | ||||||
chr3:138588296
|
G | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3558C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588296 | ||||||
chr3:138588357
|
T | C | 2 | a0002c0002t0002g0022a0002c0002t0002g0266 | 3 | HG01884.hp1 HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-6+3497A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588357 | ||||||
chr3:138588360
|
G | C | 1 | a0002c0002t0002g0267 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-6+3494C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588360 | ||||||
chr3:138588549
|
C | A | 2 | a0004c0006t0005g0030a0004c0006t0005g0031 | 2 | HG00735.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-6+3305G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588549 | ||||||
chr3:138588688
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-6+3166C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588688 | ||||||
chr3:138588789
|
G | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3065C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588789 | ||||||
chr3:138588811
|
C | A | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6+3043G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588811 | ||||||
chr3:138588846
|
G | C | 1 | a0002c0002t0002g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-6+3008C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138588846 | ||||||
chr3:138589093
|
G | C | 1 | a0003c0003t0003g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-6+2761C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589093 | ||||||
chr3:138589100
|
T | C | 2 | a0003c0003t0003g0114a0003c0003t0003g0115 | 2 | NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-6+2754A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589100 | ||||||
chr3:138589207
|
A | T | 2 | a0001c0004t0006g0029a0001c0004t0006g0032 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+2647T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589207 | ||||||
chr3:138589337
|
T | A | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(66): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-6+2517A>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589337 | ||||||
chr3:138589371
|
T | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(96): Show | 112 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-6+2483A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589371 | ||||||
chr3:138589491
|
GA | G | 7 | a0001c0001t0001g0040a0001c0004t0006g0029a0001c0004t0006g0032others(4): Show | 7 | HG00735.hp2 HG01496.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+2362delT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589491 | ||||||
chr3:138589536
|
T | C | 1 | a0003c0003t0001g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-6+2318A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589536 | ||||||
chr3:138589807
|
C | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2047G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589807 | ||||||
chr3:138589825
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+2029G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138589825 | ||||||
chr3:138590024
|
G | C | 91 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(88): Show | 105 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.-6+1830C>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590024 | ||||||
chr3:138590122
|
C | CA | 6 | a0001c0004t0006g0029a0001c0004t0006g0032a0003c0003t0001g0027others(3): Show | 6 | HG00735.hp2 HG01168.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+1731dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590122 | ||||||
chr3:138590155
|
T | C | 1 | a0001c0004t0006g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-6+1699A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590155 | ||||||
chr3:138590215
|
G | A | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+1639C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590215 | ||||||
chr3:138590246
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+1608A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590246 | ||||||
chr3:138590327
|
A | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+1527T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590327 | ||||||
chr3:138590534
|
C | T | 1 | a0002c0002t0001g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-6+1320G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590534 | ||||||
chr3:138590646
|
T | TA | 68 | a0001c0001t0001g0193a0002c0002t0002g0002a0002c0002t0002g0005others(65): Show | 80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-6+1207dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590646 | ||||||
chr3:138590712
|
G | A | 3 | a0001c0004t0004g0215a0001c0004t0004g0216a0007c0009t0004g0217 | 3 | HG03195.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-6+1142C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590712 | ||||||
chr3:138590767
|
T | C | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+1087A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590767 | ||||||
chr3:138590816
|
T | C | 7 | a0002c0002t0002g0007a0002c0002t0002g0269a0002c0002t0002g0270others(4): Show | 9 | HG02040.hp1 HG02129.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6+1038A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590816 | ||||||
chr3:138590823
|
T | TA | 21 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0194others(18): Show | 23 | HG00738.hp2 HG01123.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6+1030dupT | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590823 | ||||||
chr3:138590882
|
A | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+972T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138590882 | ||||||
chr3:138591013
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-6+841G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591013 | ||||||
chr3:138591217
|
C | A | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+637G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591217 | ||||||
chr3:138591365
|
A | AT | 70 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(67): Show | 82 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-6+488dupA | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591365 | ||||||
chr3:138591691
|
C | T | 1 | a0003c0003t0003g0034 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-6+163G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591691 | ||||||
chr3:138591851
|
T | C | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.-6+3A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 2/17 | chr3 | 138591851 | ||||||
chr3:138592034
|
A | G | 1 | a0002c0002t0002g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-108-78T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592034 | ||||||
chr3:138592126
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-108-170G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592126 | ||||||
chr3:138592359
|
T | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0212 | 3 | HG02572.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-108-403A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592359 | ||||||
chr3:138592372
|
A | G | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-108-416T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592372 | ||||||
chr3:138592518
|
C | G | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-562G>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592518 | ||||||
chr3:138592522
|
C | A | 1 | a0003c0003t0003g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-108-566G>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592522 | ||||||
chr3:138592547
|
TGGGGGTA others(7): Show |
T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-605_-108-592d others(16): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592547 | ||||||
chr3:138592577
|
A | G | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-108-621T>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592577 | ||||||
chr3:138592717
|
G | A | 1 | a0003c0003t0003g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-108-761C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138592717 | ||||||
chr3:138593228
|
T | C | 4 | a0001c0004t0004g0215a0001c0004t0004g0216a0004c0006t0005g0028others(1): Show | 4 | HG03195.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+970A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593228 | ||||||
chr3:138593239
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-109+959A>G | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593239 | ||||||
chr3:138593245
|
CAG | C | 5 | a0002c0002t0002g0005a0002c0002t0002g0219a0002c0002t0002g0220others(2): Show | 7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+951_-109+952d others(4): Show |
CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593245 | ||||||
chr3:138593289
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+909G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593289 | ||||||
chr3:138593291
|
C | T | 5 | a0001c0004t0006g0029a0001c0004t0006g0032a0004c0006t0005g0028others(2): Show | 5 | HG00735.hp2 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+907G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593291 | ||||||
chr3:138593388
|
A | T | 1 | a0004c0006t0005g0028 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-109+810T>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593388 | ||||||
chr3:138593442
|
C | T | 2 | a0003c0003t0001g0026a0003c0003t0001g0027 | 2 | HG01168.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-109+756G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593442 | ||||||
chr3:138593825
|
T | G | 58 | a0002c0002t0002g0002a0002c0002t0002g0006a0002c0002t0002g0007others(55): Show | 68 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-109+373A>C | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593825 | ||||||
chr3:138593916
|
G | T | 2 | a0002c0002t0002g0024a0002c0002t0002g0025 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-109+282C>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138593916 | ||||||
chr3:138594051
|
G | A | 11 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(8): Show | 11 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-109+147C>T | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138594051 | ||||||
chr3:138594184
|
C | T | 1 | a0006c0010t0004g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-109+14G>A | CEP70 | ENSG00000114107.9 | transcript | ENST00000264982.8 | protein_coding | 1/17 | chr3 | 138594184 |