geneid | 90799 |
---|---|
ensemblid | ENSG00000258890.8 |
hgncid | 25141 |
symbol | CEP95 |
name | centrosomal protein 95 |
refseq_nuc | NM_138363.3 |
refseq_prot | NP_612372.1 |
ensembl_nuc | ENST00000556440.7 |
ensembl_prot | ENSP00000450461.2 |
mane_status | MANE Select |
chr | chr17 |
start | 64506977 |
end | 64537946 |
strand | + |
ver | v1.2 |
region | chr17:64506977-64537946 |
region5000 | chr17:64501977-64542946 |
regionname0 | CEP95_chr17_64506977_64537946 |
regionname5000 | CEP95_chr17_64501977_64542946 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 821 | 238 | 81 | 44 | 73 | 7 | 31 | 54 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0002 | 0/0 | 821 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0003 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0004 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0005 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0006 | 0/0 | 821 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0007 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0008 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0009 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0010 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2466 | 237 | 81 | 44 | 72 | 7 | 31 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0002 | 0/0 | 2466 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0003 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0004 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0005 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0006 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0007 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0008 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0009 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0010 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
c0011 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 289 | 137 | 13 | 27 | 62 | 5 | 28 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
t0002 | 0/0 | 289 | 108 | 72 | 15 | 12 | 3 | 6 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
t0003 | 0/0 | 289 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
t0004 | 0/0 | 289 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 29 | 5 | 7 | 12 | 1 | 4 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0002 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0003 | 0/0 | 9 | 0 | 2 | 3 | 0 | 4 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0004 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0006 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0008 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0010 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0014 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2466 | 237 | 81 | 44 | 72 | 7 | 31 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0001c0009 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0002c0002 | 0/0 | 2466 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0003c0003 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0004c0005 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0005c0007 | 0/0 | 2466 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0006c0008 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0007c0006 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0008c0010 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0009c0004 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0010c0011 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2754 | 132 | 13 | 27 | 61 | 4 | 25 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0001c0001t0002 | 0/0 | 2754 | 102 | 67 | 15 | 11 | 3 | 6 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0001c0001t0003 | 0/0 | 2754 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0001c0001t0004 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0001c0009t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0002c0002t0002 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0003c0003t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0004c0005t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0005c0007t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0006c0008t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0007c0006t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0008c0010t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0009c0004t0002 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
a0010c0011t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | copy fasta | chr17 | 64501977 | 64542946 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 28 | 5 | 7 | 12 | 1 | 3 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 3 | 0 | 4 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0002 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0004 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0006 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0001c0009t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0003c0003t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0004c0005t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0005c0007t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0006c0008t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0007c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0008c0010t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0009c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
a0010c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01517 | hp2 | a0006 | c0008 | t0001 | g0080 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02129 | hp2 | a0009 | c0004 | t0002 | g0053 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02630 | hp2 | a0004 | c0005 | t0002 | g0126 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02723 | hp2 | a0003 | c0003 | t0002 | g0141 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0137 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03453 | hp2 | a0005 | c0007 | t0002 | g0041 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03654 | hp2 | a0010 | c0011 | t0001 | g0001 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03834 | hp1 | a0008 | c0010 | t0001 | g0014 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03834 | hp2 | a0007 | c0006 | t0001 | g0109 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18973 | hp2 | a0001 | c0009 | t0001 | g0025 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ASW | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0089 | REF | REF | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0121 | REF | REF | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:64519342
|
G | A | 1 | a0003 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.495G>A | p.Met165Ile | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/20 | 616/2754 | 495/2466 | 165/821 | chr17 | 64519342 | ||
chr17:64522809
|
C | T | 1 | a0010 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.823C>T | p.Pro275Ser | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/20 | 944/2754 | 823/2466 | 275/821 | chr17 | 64522809 | ||
chr17:64526195
|
G | A | 1 | a0009 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.1147G>A | p.Asp383Asn | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/20 | 1268/2754 | 1147/2466 | 383/821 | chr17 | 64526195 | ||
chr17:64529353
|
C | T | 1 | a0008 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1372C>T | p.His458Tyr | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/20 | 1493/2754 | 1372/2466 | 458/821 | chr17 | 64529353 | ||
chr17:64534646
|
G | A | 1 | a0004 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1979G>A | p.Arg660Gln | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/20 | 2100/2754 | 1979/2466 | 660/821 | chr17 | 64534646 | ||
chr17:64534675
|
T | G | 1 | a0002 | 2 | HG02258.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2008T>G | p.Tyr670Asp | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/20 | 2129/2754 | 2008/2466 | 670/821 | chr17 | 64534675 | ||
chr17:64536719
|
G | A | 1 | a0007 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2188G>A | p.Asp730Asn | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 18/20 | 2309/2754 | 2188/2466 | 730/821 | chr17 | 64536719 | ||
chr17:64537729
|
T | C | 1 | a0005 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2416T>C | p.Ser806Pro | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 20/20 | 2537/2754 | 2416/2466 | 806/821 | chr17 | 64537729 | ||
chr17:64537772
|
C | T | 1 | a0006 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.2459C>T | p.Ser820Phe | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 20/20 | 2580/2754 | 2459/2466 | 820/821 | chr17 | 64537772 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:64533122
|
A | G | 1 | a0001c0009 | 1 | NA18973.hp2 | synonymous_variant | LOW | c.1848A>G | p.Glu616Glu | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/20 | 1969/2754 | 1848/2466 | 616/821 | chr17 | 64533122 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:64507013
|
T | C | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | 111 | HG00558.hp2 HG00639.hp1 HG01069.hp2 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-85T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/20 | 85 | chr17 | 64507013 | |||||
chr17:64507093
|
G | A | 1 | a0001c0001t0004 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-5G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/20 | 5 | chr17 | 64507093 | |||||
chr17:64537905
|
A | G | 1 | a0001c0001t0003 | 2 | HG01069.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*126A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 20/20 | 126 | chr17 | 64537905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:64507365
|
C | T | 3 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150 | 3 | HG03139.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.19+249C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507365 | ||||||
chr17:64507412
|
T | C | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01175.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19+296T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507412 | ||||||
chr17:64507414
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.19+298T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507414 | ||||||
chr17:64507480
|
GCTTTTGT others(6): Show |
G | 1 | a0001c0001t0002g0034 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.19+369_19+381delTG others(11): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr17 | 64507480 | |||||
chr17:64507570
|
C | G | 10 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+454C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507570 | ||||||
chr17:64507766
|
G | C | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.19+650G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507766 | ||||||
chr17:64507809
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19+693T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507809 | ||||||
chr17:64507845
|
C | G | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19+729C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507845 | ||||||
chr17:64507917
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0140 | 6 | HG01109.hp1 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-675C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507917 | ||||||
chr17:64508115
|
G | A | 10 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0011others(7): Show | 19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.20-477G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64508115 | ||||||
chr17:64508217
|
C | G | 20 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(17): Show | 32 | HG01175.hp1 HG01243.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-375C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64508217 | ||||||
chr17:64508234
|
GTTGT | G | 10 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-355_20-352delGT others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr17 | 64508234 | |||||
chr17:64508351
|
C | G | 20 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0029others(17): Show | 32 | HG01175.hp1 HG01243.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-241C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64508351 | ||||||
chr17:64508866
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.148+146A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508866 | ||||||
chr17:64508872
|
C | T | 7 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0016others(4): Show | 15 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.148+152C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508872 | ||||||
chr17:64508916
|
C | T | 3 | a0001c0001t0002g0139a0002c0002t0002g0137a0002c0002t0002g0138 | 3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.148+196C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508916 | ||||||
chr17:64508955
|
C | G | 1 | a0004c0005t0002g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148+235C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508955 | ||||||
chr17:64508956
|
C | T | 1 | a0004c0005t0002g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148+236C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508956 | ||||||
chr17:64509040
|
C | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0007others(46): Show | 80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.148+320C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509040 | ||||||
chr17:64509222
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.148+502T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509222 | ||||||
chr17:64509319
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.148+599A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509319 | ||||||
chr17:64509402
|
C | T | 8 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0054others(5): Show | 11 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+682C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509402 | ||||||
chr17:64509405
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(6): Show | 15 | HG00438.hp1 HG00544.hp2 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.148+685G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509405 | ||||||
chr17:64509514
|
A | G | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.149-659A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509514 | ||||||
chr17:64509762
|
G | A | 1 | a0005c0007t0002g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.149-411G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509762 | ||||||
chr17:64509818
|
A | G | 1 | a0009c0004t0002g0053 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.149-355A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509818 | ||||||
chr17:64509871
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.149-302T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509871 | ||||||
chr17:64509881
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149-292G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509881 | ||||||
chr17:64509905
|
C | CTA | 13 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(10): Show | 14 | HG00639.hp1 HG01175.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.149-254_149-253dup others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr17 | 64509905 | |||||
chr17:64509960
|
T | C | 1 | a0001c0001t0002g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149-213T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509960 | ||||||
chr17:64509970
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0128 | 3 | HG02486.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.149-203G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509970 | ||||||
chr17:64510156
|
A | AT | 10 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0035others(7): Show | 13 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.149-11dupT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr17 | 64510156 | |||||
chr17:64510162
|
T | C | 34 | a0001c0001t0001g0066a0001c0001t0002g0002a0001c0001t0002g0004others(31): Show | 61 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.149-11T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64510162 | ||||||
chr17:64510169
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.149-4C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64510169 | ||||||
chr17:64510305
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.256+25T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510305 | ||||||
chr17:64510629
|
A | G | 10 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0011others(7): Show | 19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.256+349A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510629 | ||||||
chr17:64510671
|
TC | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0052 | 3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.256+394delC | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr17 | 64510671 | |||||
chr17:64510682
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0128 | 3 | HG02486.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.256+402C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510682 | ||||||
chr17:64510705
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0136 | 4 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+425A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510705 | ||||||
chr17:64510725
|
A | G | 1 | a0001c0001t0001g0028 | 2 | NA18997.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.256+445A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510725 | ||||||
chr17:64510908
|
G | A | 11 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(8): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.256+628G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510908 | ||||||
chr17:64510968
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.256+688G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510968 | ||||||
chr17:64511303
|
G | A | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.256+1023G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511303 | ||||||
chr17:64511323
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.256+1043A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511323 | ||||||
chr17:64511366
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01070.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.256+1086C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511366 | ||||||
chr17:64511386
|
T | C | 2 | a0001c0001t0002g0007a0001c0001t0002g0042 | 5 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.256+1106T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511386 | ||||||
chr17:64511396
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.256+1116C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511396 | ||||||
chr17:64511397
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.256+1117G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511397 | ||||||
chr17:64511459
|
T | C | 1 | a0001c0001t0001g0020 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.256+1179T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511459 | ||||||
chr17:64511546
|
C | A | 1 | a0001c0001t0002g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.256+1266C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511546 | ||||||
chr17:64511663
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.256+1383C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511663 | ||||||
chr17:64511802
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.256+1522C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511802 | ||||||
chr17:64511884
|
T | C | 2 | a0001c0001t0002g0017a0001c0001t0002g0052 | 3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.256+1604T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511884 | ||||||
chr17:64511895
|
G | A | 27 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(24): Show | 45 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.256+1615G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511895 | ||||||
chr17:64511920
|
T | C | 11 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0035others(8): Show | 14 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.256+1640T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511920 | ||||||
chr17:64512143
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.256+1863G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64512143 | ||||||
chr17:64512251
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.256+1971C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64512251 | ||||||
chr17:64513067
|
T | G | 10 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.257-1181T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513067 | ||||||
chr17:64513527
|
A | G | 2 | a0001c0001t0002g0040a0001c0001t0004g0051 | 2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.257-721A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513527 | ||||||
chr17:64513842
|
A | G | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.257-406A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513842 | ||||||
chr17:64513917
|
A | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0003g0011 | 4 | HG01069.hp2 HG01071.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.257-331A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513917 | ||||||
chr17:64513976
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.257-272G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513976 | ||||||
chr17:64514000
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.257-248C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514000 | ||||||
chr17:64514034
|
A | C | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.257-214A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514034 | ||||||
chr17:64514064
|
C | T | 29 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(26): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.257-184C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514064 | ||||||
chr17:64514078
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.257-170T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514078 | ||||||
chr17:64514379
|
T | G | 1 | a0001c0001t0002g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.367+21T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64514379 | ||||||
chr17:64514882
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.367+524T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64514882 | ||||||
chr17:64514918
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.367+560C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64514918 | ||||||
chr17:64514990
|
C | CCTT | 41 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(38): Show | 62 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.367+633_367+634ins others(3): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr17 | 64514990 | |||||
chr17:64515299
|
G | A | 1 | a0001c0001t0001g0010 | 4 | HG03017.hp2 HG03710.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+941G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515299 | ||||||
chr17:64515339
|
A | C | 1 | a0004c0005t0002g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.367+981A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515339 | ||||||
chr17:64515552
|
C | G | 14 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(11): Show | 29 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.368-1171C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515552 | ||||||
chr17:64515614
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.368-1109A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515614 | ||||||
chr17:64515955
|
C | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0127others(5): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-768C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515955 | ||||||
chr17:64516122
|
T | C | 2 | a0001c0001t0002g0017a0001c0001t0002g0052 | 3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.368-601T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516122 | ||||||
chr17:64516127
|
GT | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0128 | 3 | HG02486.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.368-595delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516127 | ||||||
chr17:64516156
|
A | T | 10 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.368-567A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516156 | ||||||
chr17:64516161
|
C | T | 11 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(8): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.368-562C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516161 | ||||||
chr17:64516344
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.368-379G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516344 | ||||||
chr17:64516493
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.368-230A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516493 | ||||||
chr17:64516544
|
C | A | 1 | a0009c0004t0002g0053 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.368-179C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516544 | ||||||
chr17:64517007
|
C | G | 1 | a0001c0001t0002g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.473+179C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517007 | ||||||
chr17:64517015
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.473+187C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517015 | ||||||
chr17:64517208
|
G | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0047 | 5 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+380G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517208 | ||||||
chr17:64517253
|
G | A | 1 | a0001c0001t0002g0008 | 4 | HG01257.hp2 HG01258.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+425G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517253 | ||||||
chr17:64517300
|
T | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(149): Show | 246 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.473+472T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517300 | ||||||
chr17:64517401
|
A | G | 1 | a0001c0001t0004g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.473+573A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517401 | ||||||
chr17:64517407
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.473+579A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517407 | ||||||
chr17:64517639
|
G | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0052 | 3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.473+811G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517639 | ||||||
chr17:64517672
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.473+844C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517672 | ||||||
chr17:64517673
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+845G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517673 | ||||||
chr17:64517690
|
A | AT | 15 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(12): Show | 16 | HG00639.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.473+885dupT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr17 | 64517690 | |||||
chr17:64517690
|
AT | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0072others(3): Show | 8 | HG01257.hp1 HG02129.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.473+885delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr17 | 64517690 | |||||
chr17:64517772
|
G | A | 1 | a0005c0007t0002g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+944G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517772 | ||||||
chr17:64518028
|
C | T | 11 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(8): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.473+1200C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518028 | ||||||
chr17:64518400
|
G | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0037a0001c0001t0003g0011 | 4 | HG01069.hp2 HG01071.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-921G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518400 | ||||||
chr17:64518403
|
T | C | 1 | a0001c0001t0001g0022 | 2 | NA18941.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.474-918T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518403 | ||||||
chr17:64518617
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.474-704A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518617 | ||||||
chr17:64518637
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.474-684A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518637 | ||||||
chr17:64518826
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-495G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518826 | ||||||
chr17:64518838
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.474-483G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518838 | ||||||
chr17:64518899
|
C | T | 1 | a0005c0007t0002g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-422C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518899 | ||||||
chr17:64518920
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474-401A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518920 | ||||||
chr17:64518961
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.474-360G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518961 | ||||||
chr17:64518976
|
C | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.474-345C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518976 | ||||||
chr17:64519077
|
C | T | 1 | a0001c0001t0002g0029 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.474-244C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64519077 | ||||||
chr17:64519091
|
C | G | 3 | a0001c0001t0002g0139a0002c0002t0002g0137a0002c0002t0002g0138 | 3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.474-230C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64519091 | ||||||
chr17:64519218
|
G | A | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.474-103G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64519218 | ||||||
chr17:64519535
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.589+99C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519535 | ||||||
chr17:64519605
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.589+169C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519605 | ||||||
chr17:64519817
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.589+381T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519817 | ||||||
chr17:64519866
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.589+430A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519866 | ||||||
chr17:64520123
|
T | G | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.589+687T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520123 | ||||||
chr17:64520183
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.589+747C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520183 | ||||||
chr17:64520248
|
CATT | C | 10 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+815_589+817del others(3): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr17 | 64520248 | |||||
chr17:64520458
|
CT | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(134): Show | 227 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.590-925delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr17 | 64520458 | |||||
chr17:64520520
|
C | T | 1 | a0007c0006t0001g0109 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.590-882C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520520 | ||||||
chr17:64520747
|
A | G | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-655A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520747 | ||||||
chr17:64520786
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.590-616A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520786 | ||||||
chr17:64520841
|
A | C | 1 | a0001c0001t0002g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.590-561A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520841 | ||||||
chr17:64521059
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.590-343A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521059 | ||||||
chr17:64521193
|
C | T | 1 | a0001c0001t0002g0031 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.590-209C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521193 | ||||||
chr17:64521217
|
CAA | C | 10 | a0001c0001t0001g0118a0001c0001t0002g0012a0001c0001t0002g0018others(7): Show | 13 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.590-184_590-183del others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521217 | ||||||
chr17:64521232
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.590-170G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521232 | ||||||
chr17:64521346
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.590-56G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521346 | ||||||
chr17:64521358
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.590-44A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521358 | ||||||
chr17:64521580
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0106 | 3 | NA19009.hp1 NA19011.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.715+53A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521580 | ||||||
chr17:64521867
|
A | G | 1 | a0004c0005t0002g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.715+340A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521867 | ||||||
chr17:64521874
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0065 | 5 | NA18956.hp1 NA18970.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+347C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521874 | ||||||
chr17:64521970
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.715+443C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521970 | ||||||
chr17:64522259
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.716-443T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522259 | ||||||
chr17:64522259
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-443T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522259 | ||||||
chr17:64522263
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-439A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522263 | ||||||
chr17:64522265
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-437A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522265 | ||||||
chr17:64522269
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-433T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522269 | ||||||
chr17:64522271
|
A | G | 4 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.716-431A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522271 | ||||||
chr17:64522276
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-426C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522276 | ||||||
chr17:64522276
|
C | T | 1 | a0001c0001t0002g0046 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.716-426C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522276 | ||||||
chr17:64522283
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-419C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522283 | ||||||
chr17:64522286
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-416T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522286 | ||||||
chr17:64522288
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-414T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522288 | ||||||
chr17:64522290
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-412A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522290 | ||||||
chr17:64522291
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-411G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522291 | ||||||
chr17:64522294
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-408G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522294 | ||||||
chr17:64522301
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-401G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522301 | ||||||
chr17:64522302
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-400T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522302 | ||||||
chr17:64522304
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-398T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522304 | ||||||
chr17:64522308
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-394A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522308 | ||||||
chr17:64522310
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-392G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522310 | ||||||
chr17:64522311
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-391T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522311 | ||||||
chr17:64522314
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-388C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522314 | ||||||
chr17:64522315
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-387T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522315 | ||||||
chr17:64522341
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-361A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522341 | ||||||
chr17:64522342
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-360C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522342 | ||||||
chr17:64522344
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-358T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522344 | ||||||
chr17:64522345
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-357T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522345 | ||||||
chr17:64522347
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-355A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522347 | ||||||
chr17:64522351
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-351T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522351 | ||||||
chr17:64522353
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-349C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522353 | ||||||
chr17:64522354
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-348A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522354 | ||||||
chr17:64522356
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-346C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522356 | ||||||
chr17:64522358
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-344G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522358 | ||||||
chr17:64522359
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-343G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522359 | ||||||
chr17:64522364
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-338A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522364 | ||||||
chr17:64522366
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-336T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522366 | ||||||
chr17:64522369
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-333T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522369 | ||||||
chr17:64522380
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-322A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522380 | ||||||
chr17:64522390
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-312C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522390 | ||||||
chr17:64522425
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-277T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522425 | ||||||
chr17:64522426
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-276G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522426 | ||||||
chr17:64522427
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-275A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522427 | ||||||
chr17:64522429
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-273C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522429 | ||||||
chr17:64522432
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-270A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522432 | ||||||
chr17:64522433
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-269G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522433 | ||||||
chr17:64522453
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-249G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522453 | ||||||
chr17:64522462
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-240C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522462 | ||||||
chr17:64522463
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-239G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522463 | ||||||
chr17:64522464
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-238A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522464 | ||||||
chr17:64522467
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-235C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522467 | ||||||
chr17:64522469
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-233T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522469 | ||||||
chr17:64522493
|
A | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG02015.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.716-209A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522493 | ||||||
chr17:64522504
|
A | G | 7 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0054others(4): Show | 10 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.716-198A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522504 | ||||||
chr17:64522694
|
C | T | 8 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0054others(5): Show | 11 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.716-8C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522694 | ||||||
chr17:64522979
|
CGTGTGT | C | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.909+89_909+94delGT others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64522979 | |||||
chr17:64523152
|
C | T | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.909+257C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523152 | ||||||
chr17:64523319
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.909+424A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523319 | ||||||
chr17:64523337
|
A | C | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.909+442A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523337 | ||||||
chr17:64523389
|
G | A | 8 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0127others(5): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.909+494G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523389 | ||||||
chr17:64523566
|
C | CA | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0017others(1): Show | 5 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+683dupA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64523566 | |||||
chr17:64523566
|
C | CAA | 11 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0011others(8): Show | 21 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.909+682_909+683dup others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64523566 | |||||
chr17:64523566
|
CA | C | 10 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+683delA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64523566 | |||||
chr17:64523682
|
T | C | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0007others(46): Show | 79 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(76): Show |
intron_variant | MODIFIER | c.909+787T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523682 | ||||||
chr17:64523793
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909+898A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523793 | ||||||
chr17:64523910
|
A | G | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.909+1015A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523910 | ||||||
chr17:64523965
|
A | G | 16 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(13): Show | 31 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.909+1070A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523965 | ||||||
chr17:64523968
|
T | C | 69 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(66): Show | 110 | HG00558.hp2 HG00639.hp1 HG01069.hp2 others(107): Show |
intron_variant | MODIFIER | c.909+1073T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523968 | ||||||
chr17:64524005
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.909+1110C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524005 | ||||||
chr17:64524151
|
T | G | 2 | a0001c0001t0001g0079a0006c0008t0001g0080 | 2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.909+1256T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524151 | ||||||
chr17:64524170
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.909+1275G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524170 | ||||||
chr17:64524307
|
T | G | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01175.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.909+1412T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524307 | ||||||
chr17:64524477
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.910-1293T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524477 | ||||||
chr17:64524483
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.910-1287T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524483 | ||||||
chr17:64524514
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.910-1256C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524514 | ||||||
chr17:64524551
|
C | T | 36 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(33): Show | 55 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.910-1219C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524551 | ||||||
chr17:64524609
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.910-1161C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524609 | ||||||
chr17:64524823
|
T | G | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.910-947T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524823 | ||||||
chr17:64524833
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.910-937C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524833 | ||||||
chr17:64524968
|
C | CA | 9 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0054others(6): Show | 12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-796dupA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64524968 | |||||
chr17:64525031
|
A | G | 1 | a0004c0005t0002g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.910-739A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525031 | ||||||
chr17:64525063
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.910-707G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525063 | ||||||
chr17:64525317
|
C | G | 1 | a0001c0001t0001g0022 | 2 | NA18941.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.910-453C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525317 | ||||||
chr17:64525373
|
G | C | 11 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(8): Show | 26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-397G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525373 | ||||||
chr17:64525382
|
T | C | 10 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0036others(7): Show | 12 | HG01346.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-388T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525382 | ||||||
chr17:64525513
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.910-257T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525513 | ||||||
chr17:64525645
|
A | G | 2 | a0001c0001t0001g0079a0006c0008t0001g0080 | 2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.910-125A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525645 | ||||||
chr17:64525656
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0104 | 3 | HG00673.hp2 NA18974.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.910-114C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525656 | ||||||
chr17:64525908
|
T | C | 9 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0038others(6): Show | 19 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022+26T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 9/19 | chr17 | 64525908 | ||||||
chr17:64525937
|
A | G | 10 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(7): Show | 11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1022+55A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 9/19 | chr17 | 64525937 | ||||||
chr17:64526237
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1152+37T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526237 | ||||||
chr17:64526712
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1153-399A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526712 | ||||||
chr17:64526764
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1153-347C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526764 | ||||||
chr17:64526939
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1153-172G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526939 | ||||||
chr17:64527850
|
TAA | T | 3 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02818.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1306+587_1306+588d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527850 | ||||||
chr17:64527850
|
TAATG | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0127others(1): Show | 14 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306+587_1306+590d others(6): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527850 | ||||||
chr17:64527851
|
A | T | 1 | a0001c0001t0002g0130 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1306+587A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527851 | ||||||
chr17:64527852
|
A | ATG | 4 | a0001c0001t0001g0014a0001c0001t0001g0102a0001c0001t0001g0117others(1): Show | 5 | HG00597.hp2 HG00642.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306+606_1306+607d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527852 | |||||
chr17:64527852
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1306+588A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527852 | ||||||
chr17:64527852
|
ATG | A | 5 | a0001c0001t0002g0017a0001c0001t0002g0052a0001c0001t0002g0059others(2): Show | 6 | HG02257.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+606_1306+607d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527852 | |||||
chr17:64527852
|
ATGTG | A | 10 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0034others(7): Show | 13 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306+604_1306+607d others(6): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527852 | |||||
chr17:64527860
|
G | T | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1306+596G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527860 | ||||||
chr17:64527866
|
G | GTA | 6 | a0001c0001t0002g0031a0001c0001t0002g0142a0001c0001t0002g0143others(3): Show | 7 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306+603_1306+604i others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527866 | |||||
chr17:64527866
|
G | GTATA | 5 | a0001c0001t0002g0145a0001c0001t0002g0148a0001c0001t0002g0149others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+603_1306+604i others(6): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527866 | |||||
chr17:64527866
|
GTGTGTA | G | 16 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(13): Show | 32 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1306+604_1306+609d others(8): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527866 | |||||
chr17:64527868
|
G | A | 17 | a0001c0001t0002g0017a0001c0001t0002g0031a0001c0001t0002g0033others(14): Show | 19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1306+604G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527868 | ||||||
chr17:64527870
|
G | A | 29 | a0001c0001t0001g0082a0001c0001t0001g0123a0001c0001t0002g0017others(26): Show | 31 | HG00323.hp1 HG00639.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1306+606G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527870 | ||||||
chr17:64527870
|
G | GTA | 11 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0105others(8): Show | 19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1306+627_1306+628d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527870 | |||||
chr17:64527872
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1306+608A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527872 | ||||||
chr17:64527889
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0063others(1): Show | 6 | NA18956.hp1 NA18970.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+625T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527889 | ||||||
chr17:64527891
|
T | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(13): Show | 21 | HG00597.hp2 HG00642.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1306+627T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527891 | ||||||
chr17:64527891
|
T | TAC | 27 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0022others(24): Show | 40 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1306+642_1306+643d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527891 | |||||
chr17:64527893
|
C | T | 27 | a0001c0001t0001g0101a0001c0001t0002g0002a0001c0001t0002g0007others(24): Show | 45 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1306+629C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527893 | ||||||
chr17:64527904
|
A | G | 3 | a0001c0001t0002g0139a0002c0002t0002g0137a0002c0002t0002g0138 | 3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1306+640A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527904 | ||||||
chr17:64527910
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0132 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1306+646G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527910 | ||||||
chr17:64528354
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1307-934T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528354 | ||||||
chr17:64528359
|
T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0063others(2): Show | 7 | NA18942.hp2 NA18956.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-929T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528359 | ||||||
chr17:64528478
|
A | C | 1 | a0001c0001t0002g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1307-810A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528478 | ||||||
chr17:64528628
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG00639.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1307-660C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528628 | ||||||
chr17:64528963
|
G | A | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1307-325G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528963 | ||||||
chr17:64529025
|
A | G | 1 | a0005c0007t0002g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1307-263A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64529025 | ||||||
chr17:64529060
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1307-228G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64529060 | ||||||
chr17:64529099
|
C | T | 1 | a0004c0005t0002g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1307-189C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64529099 | ||||||
chr17:64529454
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1446+27T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64529454 | ||||||
chr17:64529586
|
T | C | 50 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0007others(47): Show | 81 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.1446+159T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64529586 | ||||||
chr17:64529714
|
T | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1446+287T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64529714 | ||||||
chr17:64530064
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1446+637A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530064 | ||||||
chr17:64530122
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1446+695A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530122 | ||||||
chr17:64530176
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1446+749G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530176 | ||||||
chr17:64530178
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1447-748G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530178 | ||||||
chr17:64530250
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1447-676G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530250 | ||||||
chr17:64530342
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1447-584T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530342 | ||||||
chr17:64530482
|
A | G | 37 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(34): Show | 57 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1447-444A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530482 | ||||||
chr17:64530506
|
AT | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(147): Show | 244 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.1447-404delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr17 | 64530506 | |||||
chr17:64530546
|
C | T | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1447-380C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530546 | ||||||
chr17:64530564
|
A | G | 8 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0127others(5): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1447-362A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530564 | ||||||
chr17:64530756
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1447-170T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530756 | ||||||
chr17:64530869
|
G | T | 1 | a0001c0001t0002g0017 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1447-57G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530869 | ||||||
chr17:64531253
|
TC | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0127others(5): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1539+238delC | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr17 | 64531253 | |||||
chr17:64531526
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1540-364A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531526 | ||||||
chr17:64531587
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0007others(46): Show | 80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.1540-303G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531587 | ||||||
chr17:64531699
|
G | A | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0007others(46): Show | 80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.1540-191G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531699 | ||||||
chr17:64531705
|
T | A | 1 | a0001c0001t0001g0010 | 4 | HG03017.hp2 HG03710.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-185T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531705 | ||||||
chr17:64531757
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1540-133G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531757 | ||||||
chr17:64532061
|
A | G | 49 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0007others(46): Show | 80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.1672+39A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532061 | ||||||
chr17:64532125
|
C | CGAAGAAA others(4): Show |
1 | a0001c0001t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1672+104_1672+114d others(13): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr17 | 64532125 | |||||
chr17:64532133
|
G | GT | 10 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0011others(7): Show | 19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1672+123dupT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr17 | 64532133 | |||||
chr17:64532133
|
GT | G | 9 | a0001c0001t0001g0065a0001c0001t0002g0004a0001c0001t0002g0015others(6): Show | 19 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1672+123delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr17 | 64532133 | |||||
chr17:64532169
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1672+147T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532169 | ||||||
chr17:64532181
|
G | A | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1672+159G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532181 | ||||||
chr17:64532204
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1672+182G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532204 | ||||||
chr17:64532268
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1672+246C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532268 | ||||||
chr17:64532282
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0104 | 3 | HG00673.hp2 NA18974.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1672+260G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532282 | ||||||
chr17:64532287
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG04184.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1672+265C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532287 | ||||||
chr17:64532523
|
C | T | 3 | a0001c0001t0002g0139a0002c0002t0002g0137a0002c0002t0002g0138 | 3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1673-316C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532523 | ||||||
chr17:64532528
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1673-311G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532528 | ||||||
chr17:64532547
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1673-292G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532547 | ||||||
chr17:64532708
|
A | G | 15 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(12): Show | 30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1673-131A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532708 | ||||||
chr17:64533110
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.1843-7C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 15/19 | chr17 | 64533110 | ||||||
chr17:64533244
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1917+53C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533244 | ||||||
chr17:64533298
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1917+107C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533298 | ||||||
chr17:64533452
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1917+261A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533452 | ||||||
chr17:64533880
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1917+689C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533880 | ||||||
chr17:64533958
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1918-627C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533958 | ||||||
chr17:64534018
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1918-567C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534018 | ||||||
chr17:64534025
|
G | A | 7 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0016others(4): Show | 15 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1918-560G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534025 | ||||||
chr17:64534163
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1918-422G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534163 | ||||||
chr17:64534175
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1918-410T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534175 | ||||||
chr17:64534788
|
C | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0123 | 3 | HG00323.hp1 HG01070.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2070+51C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64534788 | ||||||
chr17:64535296
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2070+559T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535296 | ||||||
chr17:64535580
|
C | T | 9 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0054others(6): Show | 12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2070+843C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535580 | ||||||
chr17:64535582
|
A | C | 10 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0036others(7): Show | 12 | HG01346.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2070+845A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535582 | ||||||
chr17:64535694
|
A | G | 1 | a0001c0001t0002g0030 | 2 | HG01346.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2071-908A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535694 | ||||||
chr17:64535954
|
A | G | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2071-648A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535954 | ||||||
chr17:64536201
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2071-401G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536201 | ||||||
chr17:64536260
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2071-342G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536260 | ||||||
chr17:64536270
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2071-332G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536270 | ||||||
chr17:64536484
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2071-118A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536484 | ||||||
chr17:64536494
|
A | T | 1 | a0003c0003t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2071-108A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536494 | ||||||
chr17:64536504
|
T | TA | 9 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0033others(6): Show | 12 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.2071-86dupA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr17 | 64536504 | |||||
chr17:64536521
|
G | C | 8 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0054others(5): Show | 11 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.2071-81G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536521 | ||||||
chr17:64536522
|
G | T | 29 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0008others(26): Show | 48 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.2071-80G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536522 | ||||||
chr17:64536888
|
G | C | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2217+140G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 18/19 | chr17 | 64536888 | ||||||
chr17:64537510
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2290-93G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 19/19 | chr17 | 64537510 |